+ All Categories
Home > Documents > Spontaneous Pyogenic Facet Joint Infection

Spontaneous Pyogenic Facet Joint Infection

Date post: 12-Sep-2016
Category:
Upload: javier-narvaez
View: 231 times
Download: 7 times
Share this document with a friend
12
Spontaneous Pyogenic Facet Joint Infection Javier Narváez, MD, PhD,* Joan M. Nolla, MD, PhD,* José A. Narváez, MD, Laura Martinez-Carnicero, MD, Eugenia De Lama, MD, Carmen Gómez-Vaquero, MD, PhD,* Oscar Murillo, MD, José Valverde, MD, PhD,* and Javier Ariza, MD, PhD OBJECTIVE To analyze the clinical features, approaches to management, and out- come of spontaneous pyogenic facet joint infection (PFJI) in adults. PATIENTS AND METHODS Case series of 10 adults with microbiologically proven PFJI diagnosed during a 10-year period in a teaching hospital, plus a review of 32 additional cases previously reported (PubMed 1972 to 2003). Patients with prior spinal instrumentation or surgery and injection drug users were excluded. Only cases that were sufficiently detailed to be individually analyzed were included. These 32 cases, together with our 10 patients, form the basis of the present analysis. RESULTS PFJI represented nearly 20% of all spontaneous pyogenic spinal infection diagnosed in our hospital during a 10-year period. This data suggest that PFJI is more common than was previously thought. Of the 42 patients with PFJI, 26 (62%) were men and 16 (38%) were women, with ages ranging from 20 to 86 years (mean age, 59 15 years); 55% of patients were older than 60 years. The most common location of infections was the lumbosacral region (86%). All patients presented with severe back pain; fever was noted in 83% of the cases and neurological impairment in nearly 48%. In 38% of patients a systemic predisposing factor for infection was present; the most common conditions were diabetes mellitus, malignancies, and alcoholism. In almost 36% of cases, one or more concomitant infectious processes due to the same microorganism was found, mainly arthritis, skin and soft-tissue infections, endocarditis, and urinary tract infections. Staph- ylococcus aureus was the most common etiologic microorganism (86% of cases). Bacteremia was documented in 81% of the cases. The diagnosis of PFJI was based mainly on imaging study findings. Paraspinal and/or epidural extension was frequent (81% of cases), but its presence did not indicate a worse prognosis. Medical treatment alone was usually successful. The overall prognosis of PFJI was good, with a mortality rate of only 2%. The great majority of patients were cured without functional sequelae. CONCLUSION Incidence data from our institution reveal that PFJI is not a rare condi- tion, representing approximately 20% of all pyogenic spinal infections. This entity should be considered in the differential diagnosis of patients with low back pain, especially in the presence of fever, whatever the patient’s immunological status. Semin Arthritis Rheum 35:272-283 © 2006 Elsevier Inc. All rights reserved. KEYWORDS facet or interapophyseal joint, pyogenic arthritis *Rheumatology Department. †Radiology Department. ‡Infectious Diseases Department, Hospital Universitari de Bellvitge–IDIBELL, Barcelona, Spain. Address reprint requests to: Dr. Francisco Javier Narváez García, Department of Rheumatology (Planta 10-2), Hospital Universitari de Bellvitge, Feixa Llarga s/n, Hospitalet de Llobregat, Barcelona 08907, Spain. E-mail: [email protected]. 272 0049-0172/06/$-see front matter © 2006 Elsevier Inc. All rights reserved. doi:10.1016/j.semarthrit.2005.09.003
Transcript
Page 1: Spontaneous Pyogenic Facet Joint Infection

SJLCa

*†‡A

2

pontaneous Pyogenic Facet Joint Infectionavier Narváez, MD, PhD,* Joan M. Nolla, MD, PhD,* José A. Narváez, MD,†

aura Martinez-Carnicero, MD,† Eugenia De Lama, MD,†

armen Gómez-Vaquero, MD, PhD,* Oscar Murillo, MD,‡ José Valverde, MD, PhD,*nd Javier Ariza, MD, PhD‡

OBJECTIVE To analyze the clinical features, approaches to management, and out-come of spontaneous pyogenic facet joint infection (PFJI) in adults.PATIENTS AND METHODS Case series of 10 adults with microbiologically proven PFJIdiagnosed during a 10-year period in a teaching hospital, plus a review of 32additional cases previously reported (PubMed 1972 to 2003). Patients with priorspinal instrumentation or surgery and injection drug users were excluded. Onlycases that were sufficiently detailed to be individually analyzed were included.These 32 cases, together with our 10 patients, form the basis of the presentanalysis.RESULTS PFJI represented nearly 20% of all spontaneous pyogenic spinal infectiondiagnosed in our hospital during a 10-year period. This data suggest that PFJI ismore common than was previously thought. Of the 42 patients with PFJI, 26 (62%)were men and 16 (38%) were women, with ages ranging from 20 to 86 years (meanage, 59 � 15 years); 55% of patients were older than 60 years. The most commonlocation of infections was the lumbosacral region (86%). All patients presentedwith severe back pain; fever was noted in 83% of the cases and neurologicalimpairment in nearly 48%. In 38% of patients a systemic predisposing factor forinfection was present; the most common conditions were diabetes mellitus,malignancies, and alcoholism. In almost 36% of cases, one or more concomitantinfectious processes due to the same microorganism was found, mainly arthritis,skin and soft-tissue infections, endocarditis, and urinary tract infections. Staph-ylococcus aureus was the most common etiologic microorganism (86% of cases).Bacteremia was documented in 81% of the cases. The diagnosis of PFJI wasbased mainly on imaging study findings. Paraspinal and/or epidural extension wasfrequent (81% of cases), but its presence did not indicate a worse prognosis.Medical treatment alone was usually successful. The overall prognosis of PFJIwas good, with a mortality rate of only 2%. The great majority of patients werecured without functional sequelae.CONCLUSION Incidence data from our institution reveal that PFJI is not a rare condi-tion, representing approximately 20% of all pyogenic spinal infections. This entityshould be considered in the differential diagnosis of patients with low back pain,especially in the presence of fever, whatever the patient’s immunological status.

Semin Arthritis Rheum 35:272-283 © 2006 Elsevier Inc. All rights reserved.

KEYWORDS facet or interapophyseal joint, pyogenic arthritis

Rheumatology Department.Radiology Department.Infectious Diseases Department, Hospital Universitari de Bellvitge–IDIBELL, Barcelona, Spain.ddress reprint requests to: Dr. Francisco Javier Narváez García, Department of Rheumatology (Planta 10-2), Hospital Universitari de Bellvitge, Feixa Llarga s/n,

Hospitalet de Llobregat, Barcelona 08907, Spain. E-mail: [email protected].

72 0049-0172/06/$-see front matter © 2006 Elsevier Inc. All rights reserved.doi:10.1016/j.semarthrit.2005.09.003

Page 2: Spontaneous Pyogenic Facet Joint Infection

T(1(cm2it

drw

PST1

PFwauaNgalicaedsc

sopswutsp

DTsfveai(

det

LPbousget

y(jciw(

Cpiv

SCvCtWrcvo�

RTsrovPnd

ofiitt

Spontaneous pyogenic facet joint infection 273

raditionally, pyogenic arthritis of the facet (interapophy-seal) joints, also called pyogenic facet joint infection

PFJI), has been considered a rare clinical entity. Before the990s, information about this condition was very limited1-7). In the last few years, a considerable number of reportsoncerning PFJI have been published (8-34). However, sinceost reports consist of single cases (2-5,7-9,11-13,16-23,25-

9,31-34) or small series (1,6,10,14,15,24,30), certain clin-cal, microbiological, diagnostic, and therapeutic aspects ofhe disease remain to be clarified.

In this study, we present all cases of spontaneous PFJIiagnosed at our institution during a 10-year period andeview the available literature to summarize the experienceith this infectious entity.

atients and Methodstudy Sitehe study was performed at the Hospital Universitari de Bellvitge, a000-bed tertiary care teaching institution in Barcelona, Spain.

atientsrom the database of our institution, we searched for patientsith PFJI who were admitted from 1994, the first year in which

ccess to magnetic resonance imaging (MRI) in our center wasnrestricted, to 2003. Eleven patients were identified; 1 was anctive IV drug user and was excluded to homogenize the series.o cases of PFJI related to prior spinal instrumentation or sur-

ery were found. The 10 patients included had the following: (1)compatible clinical picture (back pain often accompanied by

ocalized tenderness or limited range of motion); (2) compatiblemaging findings in MRI study (synovitis/joint effusion and sub-hondral bone marrow edema in the facet joint, usually associ-ted with bone erosions and inflammatory periarticular chang-s); and (3) a microbiologically proven diagnosis. Bacteriologicaliagnosis was established on the basis of positive cultures ofpinal biopsy specimens or if blood cultures were positive. Theseases were evenly distributed throughout the study period.

In addition to these 10 cases of PFJI, 40 patients withpondylodiscitis and 2 patients with vertebral osteomyelitisf the posterior elements were diagnosed during the sameeriod, for a total of 52 cases of microbiologically provenpontaneous pyogenic spinal infection (excluding patientsith prior spinal instrumentation or surgery, injection drugsers, and those with tuberculosis or brucellosis). Informa-ion about the clinical course and microbiological features ofome of these patients with spondylodiscitis has been re-orted elsewhere (35).

ata Collectionhe medical records of the patients with PFJI were tran-cribed onto a specific form that included the following in-ormation: (1) year of diagnosis; (2) demographic data; (3)ertebral level involved; (4) clinical presentation; (5) pres-nce of fever before diagnosis, defined as an axillary temper-ture over 37.5°C; (6) predisposing factors; (7) concomitantnfectious processes; (8) erythrocyte sedimentation rate

ESR); (9) white blood cell (WBC) count; (10) bacteriologic a

iagnosis; (11) diagnostic imaging studies; (12) presence ofxtravertebral extension (epidural or paraspinal); and (13)reatment and outcome.

iterature Reviewrevious cases of PFJI reported from January 1972 to Decem-er 2003 were identified using the PubMed (National Libraryf Medicine, Bethesda, MD) search engine. The key wordssed were facet joint, interapophyseal joint, zygapophysial joint,eptic arthritis, pyogenic arthritis, and osteomyelitis. Only En-lish, French, and Spanish reports were considered; the ref-rences of the obtained studies were then examined to iden-ify additional reports.

We excluded the following: (1) patients aged under 18ears (2 cases) (13,26) or injection drug users (1 case) (19);2) 7 cases related to spinal procedures, such as therapeuticoint infiltration (20,23,32,33) or placement of epiduralatheters (10,28); and (3) 2 cases in whom no organism wassolated (32,34). Additionally, we also excluded a case inhich PFJI was the initial manifestation of spondylodiscitis

7).Finally, we also excluded the cases reported by David-

hausse and coworkers (1) and Muffoleto and coworkers (6atients; 2 of them IV drug abusers) (30) because their clin-

cal characteristics were not sufficiently detailed to be indi-idually analyzed.

tatistical Analysisontinuous data were described as mean � standard de-iation (SD) and categorical variables as percentages.omparisons between groups were made using Student t

est for independent continuous variables or the Mann–hitney U test when the assumption of normality was not

ealized. To analyze categorical data, we performed thehi-square test or Fisher’s exact test when the expectedalues were less than 5. Correlations were made by meansf Spearman’s test. Statistical significance was defined as P

0.05.

esultshe main characteristics and outcome of the 10 patients withpontaneous PFJI diagnosed in our institution are summa-ized in Tables 1 and 2; their mean age was similar to the restf patients with pyogenic spinal infection (60 � 14 yearsersus 64 � 14 years, respectively; P � nonsignificant [NS]).FJI represented nearly 20% (10/52) of all cases of sponta-eous pyogenic spinal infection diagnosed in our hospitaluring a 10-year period.In addition to our 10 cases, 32 well-documented cases

f spontaneous PFJI in adult nondrug users were identi-ed in the literature. In all cases, the infection occurred

ndependently of spondylodiscitis. Details of these pa-ients are summarized in Tables 3 and 4. Thus, includinghe patients presented here, a total of 42 cases were avail-

ble for review.
Page 3: Spontaneous Pyogenic Facet Joint Infection

DOwtw1w

VAag

sTo(

CPaw

s(

T

C

T

C

*

274 J. Narváez et al

emographic Dataf the 42 patients, 26 (62%) were men and 16 (38%) wereomen (male:female ratio of 1.6), with ages ranging from 20

o 86 years (mean, 59 � 15 years). The age at onset of PFJIas similar in men and women (58 � 16 years versus 60 �3 years, respectively; P � NS). Fifty-five percent of patientsere older than 60 years (see Table 5).

ertebral Level Involvedll patients had unilateral facet joint involvement, mainlyffecting the right side (55% of cases). The lumbosacral re-ion was affected in 86% (36/42) of the cases, the cervical

able 1 Clinical Characteristics of Our Patients

Patients YearAge/Sex

(yrs)Vertebral Le

Involved

1 1996 33/M Left L4–L5

2 1997 46/M Right L5–S3 1998 60/F Right L4–L4 1998 74/M Right L5–S

5 2000 70/F Left C2–C36 2001 70/F Right L1–L7 2001 82/M Left L1–L28 2002 54/M Right T8–T99 2003 54/F Right L3–L

10 2003 59/F Right L3–L

OPD, chronic obstructive pulmonary disease; DM, diabetes mellituwhite blood cell count.

able 2 Bacteriological Diagnosis, Extravertebral Complicatio

Patients OrganismEpiduralAbscess

ParA

1 Staphylococcus aureus Yes

2 S. aureus Yes3 S. aureus No

4 S. aureus Yes

5 Streptococcus agalactiae No

6 S. aureus Yes7 Enterococcus faecalis Yes

8 S. aureus Yes

9 S. aureus Yes

10 S. agalactiae No

T, computed tomography; IV, intravenous; MRI, magnetic resonanpyrophosphate isotope scan.

pine in 9.5% (4/42), and the thoracic spine in 4.5% (2/42).he most commonly involved site was the L4-L5 level (40%f cases), followed by the L3-L4 level (17%), and L5-S1 level14%).

linical PresentationFJI was community-acquired in 93% (39/42) of the casesnd nosocomial in 7% (3/42). All nosocomial cases of PFJIere related to infection of indwelling vascular catheters.The mean duration of symptoms before hospital admis-

ion was 36 � 45 days (range, 2 days to 6 months). In 69%29/42) of the cases, the average duration of symptoms

Duration ofSymptoms beforeDiagnosis (days) Clinical Presentation

7 Low back pain

16 Low back pain5 Low back pain2 Low back pain

4 Cervical pain21 Low back pain15 Low back pain5 Dorsal pain � paraparesis5 Back pain � radiculopathy2 Low back pain

, erythrocyte sedimentation rate; UTI, urinary tract infection; WBC,

eatment, and Outcome

ebralss

PsoasAbscess

BloodCultures

Spinal SpecimenCulture*

No � ND

No � NDNo � ND

No � ND

No � ND

No � NDYes � ND

No � �

No � ND

No � ND

ging; ND, not done; 67Ga, gallium-67 citrate scan; 99Tc, technetium

vel

151

2

44

s; ESR

ns, Tr

avertbsce

Yes

YesYes

Yes

No

NoYes

Yes

Yes

No

ce ima

Spinal abscess obtained by CT-guided biopsy or by surgery.

Page 4: Spontaneous Pyogenic Facet Joint Infection

bctfe

pacgtpwt

itnp

PIptmil

T

taneou

T

S

UC

UU

E

C

Spontaneous pyogenic facet joint infection 275

efore diagnosis was less than 1 month. No significantorrelation between the age of the patients and the dura-ion of symptoms was found. No significant difference wasound in the duration of symptoms among the differenttiologic agents.

Clinically, severe pain was the presenting complaint in allatients. Presentations ranged from subacute to acute, and inll cases pain became constant without relief with rest. Inases of PFJI involving the thoracic or lumbar spine, pain wasenerally unilateral, usually radiating into the flank or but-ocks, and was often accompanied by muscle spasm andainful palpation of the paravertebral musculature. Patientsith cervical involvement were clinically characterized by

he presence of torticollis and a palpable mass.

able 1 Continued

Fever Predisposing Factor(s)C

Yes None Infer

Yes None NoYes Non-insulin-dependent DM MeYes Lymphoma, prior infectious

phlebitis, and staphylococcalbacteremia (2 months earlier)

Rig

Yes Metastatic breast cancer AcuYes None LefNo COPD UTYes None NoYes None NoYes Hepatic cirrhosis Cu

able 2 Continued

Other Site ofIsolation

DiagnosticImaging Studies

ynovial fluid 67Ga, 99Tc, MRI IV cloxacgentam

rine 67Ga, 99Tc, CT, MRI IV cloxacerebrospinal fluid MRI IV cloxac

gentam67Ga, 99Tc, MRI IV cloxac

and cip67Ga, 99Tc, MRI IV penicil

2 weekrine 67Ga, 99Tc, MRI IV cloxacrine 67Ga, 99Tc, MRI IV ampici

weeks;weeks

pidural/paravertebralabscess

MRI IV cloxac

67Ga, 99Tc, MRI IV cloxacoral rifaweeks

utaneous ulcer MRI IV penicil2 week

Fever was noted in 83% (35/42) of the cases. Neurologicmpairment was present in nearly 48% (20/42) of the pa-ients: 16 (38%) had radiculopathy, and 4 (9.5%) had severeeurologic deficits (hemiparesis in 1 patient, paraparesis in 1atient, and cauda equina syndrome in 2 patients).

redisposing Factorsn 38% (16/42) of the patients, 1 or more systemic predis-osing factors for infection were found. In 33% (14/42) ofhe cases, the predisposing factor was an underlying im-unosuppressive disease; the most common associated

llnesses were diabetes mellitus, malignancies, chroniciver diseases, and alcoholism (see Table 6). Patients with

mitant InfectiousProcess

ESR(mm/h)

WBC(�109/L)

s olecranon bursitis,rist arthritis

92 14,000

140 19,950is 74 7660rnoclavicular arthritis 90 6005

b lymphangitis 74 9700t arthritis 121 11,910carditis 63 9700

47 15,48098 11,140

s ulcer 79 7150

biotic Treatment Surgery Outcome

r 6 weeks (with IVring the first week)

No Recovered

r 6 weeks No Recoveredr 6 weeks (with IVring the first week)

No Recovered

r 4 weeks; oral rifampicincin for 2 weeks

No Recovered

4 weeks; oral amoxicillin for No Recovered

r 6 weeks No RecoveredIM streptomycin for 2picillin � ceftriaxone for 4

No Recovered

r 6 weeks Yes Paraparesis

oral rifampicin for 2 weeks;n and levofloxacin for 4

No Recovered

4 weeks; oral amoxicillin for No Recovered

onco

ctiouight wneningitht ste

te limt wrisI, endonene

Anti

illin foicin duillin foillin foicin duillin forofloxalin forsillin follin �IV am

illin fo

illin �mpici

lin fors

Page 5: Spontaneous Pyogenic Facet Joint Infection

uofvtso

CItfcd

T

D eumat

276 J. Narváez et al

nderlying immunosuppressive diseases were on averagelder than patients without these conditions, but the dif-erence was not statistically significant (61 � 14 yearsersus 57 � 16 years, respectively; P � NS). Finally, 5% ofhe patients (2/42) had an extraspinal infection due to theame microorganism several months before the diagnosis

able 3 Clinical Characteristics of 32 Reported Adult Cases

Patient(Reference) Year

Age/Sex(yrs)

VertebralLevel

Involved Feve

1 (2) 1987 66/M Right L3–L4 Yes2 (3) 1987 45/F Left L4–L5 No3 (4) 1988 66/M Left L4–L5 No

4 (5) 1989 65/M Right L2–L3 Yes

5 (6) 1989 63/F Left C4–C5 No

6 (6) 1989 63/M Left C4–C5 No7 (6) 1989 82/M Left L4–L5 Yes8 (8) 1991 76/M Right C1–C2,

odontoidprocess

Yes

9 (9) 1992 68/M Left L3–L4 Yes10 (10) 1992 59/M Left L5–S1 Yes11 (11) 1993 71/F Right L4–L5 Yes12 (12) 1995 61/M Right L4–L5 Yes

13 (14) 1996 23/M Left L5–S1 Yes14 (14) 1996 62/M Right L2–L3 Yes15 (14) 1996 20/M Right L4–L5 Yes16 (15) 1997 60/F Left L5–S1 Yes17 (15) 1997 63/M Right L4–L5 Yes

18 (15) 1997 74/F Right L3–L4 Yes19 (15) 1997 49/M Left L2–L3 Yes20 (15) 1997 66/F Right L4–L5 Yes21 (15) 1997 63/M Right L4–L5 Yes22 (16) 1997 55/F Left L5–S1 Yes23 (17) 1997 41/F Left L4–L5 Yes24 (18) 1998 56/M Left L4–L5 Yes25 (21) 2000 38/M Right L3–L4 Yes

26 (22) 2000 54/F Right L4–L5 Yes

27 (24) 2000 42/M Right T3–T4 Yes28 (24) 2000 65/M Left L4–L5 Yes29 (25) 2000 35/F Right L2–L3 Yes 30 (27) 2001 86/F Left L4–L5 Yes31 (29) 2001 66/M Right L3–L4 No32 (31) 2002 73/M Left L4–L5 No

M, diabetes mellitus; NA, data not available; PMR, polymyalgia rh

f PFJI. v

oncomitant Infectious Processesn 36% (15/42) of patients, 1 or more concomitant infec-ious processes due to the same microorganism wereound (Table 7). Patients with concomitant infectious pro-esses were on average older than those without, but theifference was not statistically significant (60 � 15 years

ntaneous PFJI (1972–2003)

redisposingFactor(s)

ConcomitantInfectiousProcess

ESR(mm/h)

WBC(�109/L)

ne None 99 11,370ne None 73 6500lebitis and

staphylococcalbacteremia 4months earlier

None 113 7700

eroid treatment(PMR)

None 46 7400

, livercirrhosis,alcoholism

None NA NA

, alcoholism None 103 15,200ne None 83 5300ne None NA 11,000

ne None 80 6700ne UTI 108 14,300ne None NA NAne Right

sternoclaviculararthritis

95 14,000

lenectomy None NA 13,000coholism None 56 22,400ne None 54 12,500ne None 70 8500

Chronicosteomyelitis

125 11,000

ne Buttock abscess 76 9000ne None NA NAne None 108 7600

UTI 66 11,700ne None 95 7200ne UTI NA 22,500ne None NA 17,000ng-termhemodialysis

Soft tissueabscess

NA 11,700

rcinoma insitu of thecervix

None 135 20,000

ne None NA NAne None NA NAne None 51 NAne Endocarditis 72 NAne None 88 24,500

None 140 NA

ica; UTI, urinary tract infection; WBC, white blood cell count.

of Spo

rP

NoNoPh

St

DM

DMNoNo

NoNoNoNo

SpAlNoNoDM

NoNoNoDMNoNoNoLo

Ca

NoNoNoNoNoDM

ersus 57 � 15 years, respectively; P � NS). The fre-

Page 6: Spontaneous Pyogenic Facet Joint Infection

qpc[

LD((a5(

TR

A*†

TP

>80 3 (6)

Spontaneous pyogenic facet joint infection 277

uency of underlying conditions causing immunosup-ression was higher in the subgroup of patients with con-omitant infectious processes (50% [8/16] versus 31%8/26], respectively; P � 0.05).

aboratory Testsata about ESR were available in 32 patients; it was elevated

above 30 mm/h) in all cases. Mean ESR was 88 � 26 mm/hrange 46 to 140 mm/h). Data about WBC count were avail-ble in 34 patients. The mean WBC count was 12,081 �111 � 109/L (range, 5300 to 24,500 � 109/L). In 53%

ent, and Outcome of 32 Adult Cases of Spontaneous PFJI

ParaspinalExtension BC

SpinalSpecimen

Culture* Treatment

No � ND ATBNo � � ATBNo � � ATB � SurgeryYes � � ATB � SurgeryNo NA � ATB � Surgery

Yes NA � ATB � SurgeryNo � ND ATB

� � ATB � SurgeryYes � � ATBYes � ND ATBYes � ND ATBYes � ND ATBYes � � ATBYes � ND ATBNo � ND ATBYes � � ATBYes � ND ATBNo � � ATBYes � ND ATBYes � NA ATB � SurgeryYes � ND ATBYes NA � ATBYes � � ATB � Surgery

Yes NA � ATBYes � NA ATB � SurgeryYes NA � ATB � SurgeryYes � ND ATBNo � ND ATBYes � � ATBYes � ND ATBYes � ND ATBNo � � ATB � Surgery

a not available; ND, not done.

able 4 Bacteriological Diagnosis, Extravertebral Extension, Treatmeported Previously (1972–2003)

Patient(Reference) Organism

EpiduralExtension

1 (2) Staphylococcus aureus No2 (3) S. aureus Yes3 (4) S. aureus Yes4 (5) S. aureus Yes5 (6) Staphylococcus epidermidis

and Propionibacteriumsp.

No

6 (6) S. aureus No7 (6) S. aureus No8 (8) S. aureus9 (9) Klebsiella pneumoniae No

10 (10) S. aureus No11 (11) S. aureus No12 (12) S. aureus No13 (14) S. aureus No14 (14) S. aureus Yes15 (14) S. aureus Yes16 (15) S. aureus Yes17 (15) S. aureus Yes18 (15) S. aureus No19 (15) S. aureus Yes20 (15) S. aureus Yes21 (15) S. aureus Yes22 (16) S. aureus Yes23 (17) S. aureus, Streptococcus

viridans, and Neisseriasubflava

Yes

24 (18) S. aureus Yes25 (21)† S. aureus Yes26 (22) S. aureus Yes27 (24) S. aureus Yes28 (24) S. aureus No29 (25) S. aureus No30 (27) S. aureus No31 (29) S. aureus Yes32 (31) Streptococcus agalactiae

(GBS)Yes

TB, antibiotic; BC, blood cultures; GBS, group B streptococcus; NA, datSpinal specimens obtained by CT guided biopsy or by surgery.All patients survived except for patient 25

able 5 Age Distribution in 42 Patients with SpontaneousFJI

Age (year) Number of Patients (%)

18–30 2 (5)31–40 3 (6)41–50 5 (14)51–60 9 (21)61–70 15 (36)71–80 5 (12)

18/34) of cases, WBC count was above 11 � 109/L.

Page 7: Spontaneous Pyogenic Facet Joint Infection

BTcw

nmla

(wfws

cposn

ac

IA(bstt

sictccbctfnt

bdwtisvCnc

4a

To

U

P

C*†

TS

A

USECIML

*

Tt

S

S

G

M

*

278 J. Narváez et al

acteriological Diagnosishe infection was monomicrobial in 95% (40/42) of theases; in 5% (2/42) of patients more than 1 microorganismas responsible for the process.The causative microorganisms in the 42 cases of sponta-

eous PFJI are listed in Table 8. Staphylococcus aureus was theost common etiologic organism (86% of the cases), fol-

owed by Streptococcus species (9% of the cases); Gram-neg-tive organisms were responsible for 2% of the cases.

Blood cultures gave positive results in 81% of the cases30/37) in which this information was reported. In patients inhom an associated infectious process was observed, the

requency of positive blood cultures was higher than in thoseho did not present with this condition (100% [16/16] ver-

us 68% [15/21], respectively; P � 0.05).Etiologic diagnosis was established on the basis of blood

ultures alone in 62% (26/42) of the cases; in 29% (12/42) ofatients the etiological diagnosis was established on the basisf positive cultures of spinal specimens, obtained by ultra-ound or computed tomography (CT) -guided percutaneouseedle biopsy, or by surgery. In 4 patients (9%), both blood

able 6 Predisposing Factors in 42 Patients with Spontane-us PFJI

Risk FactorNumber of

Patients (%)

nderlying immunosuppressive disease*Diabetes mellitus 6 (14)Malignancy† 3 (7)Alcoholism 3 (7)Chronic liver disease 2 (5)End-stage renal disease/Long-term

hemodialysis1 (2)

Splenectomy 1 (2)COPD 1 (2)Chronic steroid treatment 1 (2)

rior extraspinal infection 2 (5)

OPD, chronic obstructive pulmonary disease.Three patients had more than 1 process.Carcinoma of the cervix (1 patient), lymphoma (1 patient), and

breast cancer (1 patient).

able 7 Concomitant Infectious Processes in 42 Patients withpontaneous PFJI*

Process Number of Patients (%)*

rthritis 4 (10)Peripheral arthritis 2 (5)Sternoclavicular arthritis 2 (5)rinary tract infection 4 (10)kin and soft-tissue infections 3 (7)ndocarditis 2 (5)hronic osteomyelitis 1 (2)

nfectious bursitis 1 (2)eningitis 1 (2)

ymphangitis 1 (2)

a

nd spinal cultures were positive, identifying the same mi-roorganism.

maging Testsll patients underwent plain radiography of the spine, 29

69%) had CT, 29 (69%) had MRI, 26 (62%) had technetiumone scans, 11 (26%) had gallium scans, and 1 (2%) hadingle-photon emission computed tomography (SPECT). Inhe majority of cases, a combination of studies was employedo reach the diagnosis.

Plain radiographs were usually of no value in the firsttages of the disease. Technetium-99 scintigraphy showedncreased uptake of tracer at the involved vertebral level in allases tested, as early as 3 days after symptom onset. In con-rast to spondylodiscitis, the uptake was usually more verti-ally oriented than horizontally, although in the majority ofases it was difficult to distinguish between the 2 conditionsased only on scintigraphy findings. SPECT was used in 1ase to show more clearly that the infection was in the pos-erior elements. Gallium-67 scintigraphy was positive foracet joint infection in 82% (9/11) of the cases tested; the 2egative scans were obtained at 3 days and 5 weeks, respec-ively, after the beginning of symptoms.

In all patients CT and/or MRI was performed. MRI wasoth sensitive and specific in diagnosing PFJI as early as 2ays after the onset of symptoms, especially when enhancedith gadolinium. By contrast, CT can appear normal early in

he disease. In the present series CT only detected abnormal-ties after 2 weeks of symptoms. Both imaging techniqueshowed additional information about the presence of extra-ertebral extension (epidural, paraspinal, or psoas abscess).T scan was also of great value in guiding percutaneouseedle biopsies of the paravertebral abscesses or of the con-erned facet joint.

Paraspinal and/or epidural extension was seen in 81% (34/2) of the patients: paraspinal alone (paravertebral musclesnd/or psoas muscle) in 21% (9/42) of the patients, epidural

able 8 Causative Microorganisms in 42 Patients with Spon-aneous PFJI*

BacteriaNumber ofCases (%)

taphylococciStaphylococcus aureus 36 (86)Staphylococcus epidermidis 1 (2)

treptococciStreptococcus agalactiae 3 (7)Streptococcus viridans 1 (2)ram-negative bacilliKlebsiella pneumoniae 1 (2)iscellaneousPropionibacterium sp 1 (2)Neisseria subflava 1 (2)Enterococcus faecalis 1 (2)

Two patients had polymicrobial infection.

lone in 12% (5/42), and both in 48% (20/42) of the patients.

Some patients had more than 1 process.
Page 8: Spontaneous Pyogenic Facet Joint Infection

Twsfiohns

TAml8Cawpsma

iroc

DIttopau

2TDwpimcMmp

nstWPnpa

tamfcrtta

dsdrnttsmtddsdt

mcipsn

tTwaTvi

wiut

strismc

sB

Spontaneous pyogenic facet joint infection 279

hus, in nearly 60% (25/42) of the cases, epidural extensionas found. All patients with neurologic impairment pre-

ented with extravertebral extension, but the presence of thisnding was not necessarily associated with the developmentf neurologic symptoms. There was no association betweenigh leukocyte count and the presence of epidural or paraspi-al extension. Diagnostic delay and etiologic agents wereimilar in patients with and without extravertebral extension.

reatment and Outcomell patients initially received parenteral antibiotics, with aean duration of 4 weeks (range, 1 to 6 weeks), often fol-

owed by oral therapy (mean 1 � 3 months; range, 2 weeks tomonths). In addition to antibiotic treatment, percutaneousT-guided drainage of the infected joint and/or paraspinalbscess was performed in 19% (8/42) of the patients. Surgeryas indicated in 26% (11/42) of the patients, mainly in theresence of severe neurologic dysfunction. Bed rest was pre-cribed in all cases for at least 3 weeks; usually, when move-ent was authorized, external immobilization was indicated

t least during the first month.One of the 42 patients died due to an asystolic arrest dur-

ng surgery. Of the remaining 41 patients, 1 became parapa-etic; the rest were cured without functional sequelae or withnly residual pain, which did not impede an active life. Noases relapsed.

iscussionn this study we present the largest published series of pa-ients with PFJI seen in a tertiary care institution and reviewhe available literature in an effort to increase the knowledgef this disease. To standardize the information, patients withrior spinal instrumentation or surgery, injection drug users,nd pediatric patients were excluded, since all of these pop-lation groups present specific differential characteristics.Data from our institution reveal that PFJI represents nearly

0% of the cases of spontaneous pyogenic spinal infections.his prevalence is higher than that previously reported byavid-Chausse and coworkers (1) and Muffoletto and co-orkers (30) in the 1980s. These discrepancies may be, inart, attributed to methodologic differences but, in our opin-

on, it is mainly a consequence of the routine employment ofore sensitive imaging techniques during recent years. PFJI

ould easily be misdiagnosed as spondylodiscitis if CT orRI is not used. Similarly, some epidural infections or psoasuscle abscesses believed to be primary may in fact be com-lications of unrecognized PFJI.The demographic characteristics of patients with sponta-

eous PFJI were similar to those reported with spontaneouspondylodiscitis (35-42). Data from this review demonstratehat PFJI mainly appears in patients over the age of 60 years.

e did not find differences between the age of patients withFJI and the rest of patients with spontaneous pyogenic spi-al infections diagnosed at our hospital during the studyeriod. As occurs in the majority of osteoarticular infections,

male predominance was seen. b

As in spondylodiscitis (35-42), PFJI is most common inhe lumbosacral area. Of interest, three-quarters of the casesre located between L3 and S1, the L4-L5 level being theost common site involved. Patients with PFJI are usually

ebrile and present with severe pain and stiffness that be-omes constant without relief upon resting. The presence ofadicular symptoms is relatively frequent (in nearly 40% ofhe cases), probably as a consequence of the localization ofhe infectious process; however, severe neurologic deficitsre rare, occurring in less than 10% of the cases.

It is difficult to differentiate between PFJI and spondylo-iscitis based only on clinical grounds. There are, however,ome clues that may be useful. When compared with spon-ylodiscitis, PFJI symptoms tend to be unilateral, usuallyadiating into the flank or buttocks, and are often accompa-ied by muscle spasm and painful palpation of the paraver-ebral musculature. In addition, the mean duration of symp-oms before diagnosis of PFJI is shorter than those reported inpondylodiscitis (35-42). In PFJI, symptoms tend to presentore acutely and with greater severity in the early stages. In

he absence of neurologic deficit or fever, a patient may beiagnosed with acute lumbago if further investigation is notone. Thus, in uncomplicated cases a high degree of clinicaluspicion is necessary. In Table 9 we summarized the mainifferences and similarities between PFJI and spondylodisci-is according to our experience (35).

Of interest, no systemic risk factors for PFJI are detected inore than 60% of patients, indicating that spontaneous PFJI

an also affect immunocompetent patients without debilitat-ng conditions. When underlying medical illnesses areresent, they are similar to those observed in spontaneouspondylodiscitis (35-42), including diabetes mellitus, malig-ancies, alcoholism, and chronic liver diseases.In nearly 36% of patients, 1 or more concomitant infec-

ious processes due to the same microorganism were found.his subgroup of patients was on average older than thoseithout them. Moreover, in most of these cases, bacteremia

nd underlying immunosuppressive illness were present.he most common diagnoses were peripheral and sternocla-icular arthritis, skin and soft-tissue infections, urinary tractnfections, and endocarditis.

Laboratory data also are similar to those found in patientsith spondylodiscitis. Leukocyte count is elevated in approx-

mately 50% of cases. The ESR is uniformly elevated, being aseful parameter for monitoring the course of the disease andhe response to treatment.

Regarding etiologic diagnosis, the causal microorganism inpontaneous PFJI is typically S. aureus, accounting for 86% ofhe reported cases, a prevalence clearly higher than the oneeported in the series of spondylodiscitis (35,36,38-42). Ofnterest, Gram-negative bacilli, an important pathogen inpondylodiscitis of the elderly (35,36,41-43), are an uncom-on cause of spontaneous PFJI, producing only 2% of the

ases.Hematogenous spread from a distant focus is the pre-

umed route of infection in the cases of spontaneous PFJI.acteremia was demonstrated in 81% of the cases in which

lood culture results were available, stressing the usefulness
Page 9: Spontaneous Pyogenic Facet Joint Infection

oaeabcmn

o(ipdt

tp

Pcbna(parid

T

D

L

C

E

I

280 J. Narváez et al

f this microbiological technique to establish the causativegent. In fact, in 62% of patients the etiologic diagnosis wasstablished on the basis of blood cultures, since PFJI is almostlways a monomicrobial disease and isolates from positivelood cultures can be assumed to be responsible for the pro-ess. When blood cultures are negative, spinal specimensust be obtained, preferably by CT-guided percutaneouseedle biopsy, or by open surgical biopsy when necessary.Several cases of PFJI have been described as a complication

f spinal procedures, such as therapeutic joint infiltration20,23,32,33) or placement of epidural catheters (10,28). Its strange that the number of these cases is not higher (7atients), taking into account the number of invasive proce-ures that are performed in the lumbar region. Thus, al-

able 9 Comparison of PFJI and Spondylodiscitis

PFJI

emographiccharacteristics

Mainly in patients over 60Male predominance (62%)

Predisposing factor for inf38% of the cases

ocation Lumbar spine: 86%Cervical spine: 9.5%Thoracic spine: 4.5%

linical presentation Usually acute onset

Unilateral inflammatory painto the flank or buttockmarked muscle spasm

Limited range of spinal mo

Fever: 83%

Neurologic deficits: 38% (radiculopathy)

tiologic agents S. aureus: 86%Streptococci: 12%Gram-negative bacilli: 2%

maging Radiography: in general ndiagnosis

Scintigraphy: difficult to dbetween the 2 conditionvertically oriented

MRI (or CT) is generally nobtain an accurate diag

Extravertebral extension: 8Paraspinal: 26%Epidural: 15%Both: 59%

hough rare, PFJI should be suspected as a complication of e

hese interventions in patients whose pain worsens after therocedure, especially if fever appears.Data from this review demonstrate that the diagnosis of

FJI was based mainly on imaging study findings and thatlinical data failed in the majority of cases to discriminateetween PFJI and spondylodiscitis. Plain films are, in general,ot useful for diagnosis, since the radiologic abnormalitiesppear 6 to 12 weeks after the onset of symptoms2,4,12,15,18,30). The signs that appear earlier in obliquelain radiographs are soft-tissue swelling, with narrowingnd irregularity of joint space. Technetium-99 bone scintig-aphy seems to be 100% sensitive in detecting facet jointnvolvement, but is not specific (12,14). In contrast to spon-ylodiscitis, the uptake in PFJI is usually more vertically ori-

Spondylodiscitis

(55%)

in

Mainly in patients over 60 years (60%)Male predominance (56%)

Predisposing factor for infection in50% of the cases

Lumbar spine: 66%Thoracic spine: 28%Cervical spine: 6%

iating

Subacute or insidious onset

Diffuse back pain, inflammatory (75%)or mechanical (25%)

Limited range of spinal motion andlocalized spinal tenderness

Fever: 63%

Neurologic deficits: 28% (mainlyradiculopathy)

S. aureus: 39%Gram-negative bacilli: 39%Streptococci: 19%Other organisms: 3%

ful for

ishake

ary to

Radiography: frequently provides thediagnosis

Scintigraphy: uptake horizontallyoriented

MRI is the imaging modality of choice,but in many cases the diagnosis canbe made on the basis of CT and/orscintigraphy

Extravertebral extension: 74%Paraspinal: 41%Epidural: 13%Both: 46%

years

ection

in, rads, with

tion

mainly

ot use

istingus; upt

ecessnosis

1%

nted than horizontally oriented (3,5,10,12,15). Gallium-67

Page 10: Spontaneous Pyogenic Facet Joint Infection

Spontaneous pyogenic facet joint infection 281

Figure 1 Pyogenic arthritis of the right L5-S1 facet joint. A. Enhanced CT scan shows joint destruction, with wideningof the joint space and erosive changes (white arrows). There is also periarticular inflammatory changes, without clearfluid collections, in the corresponding foramina and posterior paraspinal muscles (black arrowheads), as well as in theepidural space (black arrows). B. Sagittal T1-weighted MR image demonstrates bone marrow edema and irregularity ofthe joint surfaces (short arrows), and extensive periarticular inflammatory changes in the posterior paraspinal muscles(long arrows) and in the neural foramina. C. sagittal short tau inversion recovery (STIR) MR image better depicts the

joint and periarticular inflammatory changes.
Page 11: Spontaneous Pyogenic Facet Joint Infection

stSptMoeumftsisMtt4satesea

wot

fdwepq

oiawor

diaotpue

demo(m

oqal

R

1

FTbcc

282 J. Narváez et al

cintigraphy may be falsely negative in cases of PFJI if ob-ained earlier than 1 week after symptom onset (8,12).PECT can be used to confirm that the infection is in theosterior elements (5,32), but currently this is still a researchool. The most useful imaging techniques in PFJI are CT and

RI. CT is the investigation that best delineates the extent ofsseous lesions of the facet joints, but may appear normalarly in the disease (25,44,45). For this reason, it is moreseful in patients with subacute or chronic illness. CT abnor-alities include loss of subchondral bone associated with the

acet joint, loss of ligamentum flavum density, and oblitera-ion of fat planes. The presence of paraspinal soft-tissue le-ions and/or collections can also be detected by CT usingntravenous injection of contrast; however, CT depiction ofoft-tissue structures is less sensitive than MRI (44-46).oreover, CT provides radiologic guidance for interven-

ional procedures (ie, biopsy, drainage). MRI is consideredhe modality of choice for diagnosis of PFJI (18,30,34,45-8). High-quality MRI with gadolinium enhancement is bothensitive and specific in diagnosing PFJI as early as 2 daysfter the onset of symptoms (18), ruling out involvement ofhe disc space and vertebral body. Moreover, it is especiallyffective for evaluating the neural structures of the spine (ie,pinal cord, nerve roots) and the spread of infection to thepidural space and/or paraspinal soft tissues (see Figs. 1nd 2).

Paraspinal and/or epidural extension are a frequent findinghen MRI and/or CT are used for the diagnosis of PFJI (81%f patients in this review). As other authors (49), we used the

igure 2 Pyogenic arthritis of the left L5-S1 facet joint. An axial2-weighted MR image shows widening of the joint space, occupiedy fluid, and a well-defined fluid collection in the paraspinal mus-les (long arrows) corresponding to an abscess. Note also small fluidollection in the posterior epidural space (short arrows).

erm extension, since we did not attempt to differentiate dif-

use inflammation or granulation tissue from a true abscess,ue to the retrospective nature of our study. No relationshipas found between extension and clinical findings. Its pres-

nce did not indicate a worse prognosis; in fact, in mostatients, this radiologic finding had no clinical conse-uences.The therapeutic approach to PFJI should be based mainly

n the clinical manifestations and not on the imaging find-ngs. In our experience, medical treatment alone, includingntibiotic therapy, bed rest for 3 weeks, and immobilizationith orthosis during the first month, is suitable for most casesf PFJI. Surgical intervention is indicated when severe neu-ologic dysfunction is present.

The optimal duration of therapy for PFJI has not been wellefined, since all reports are retrospective. Usually, antibiot-

cs are given initially intravenously for at least 4 weeks, andfter this parenteral treatment, the majority of clinicians usesral antibiotics for several weeks. Probably a total period of 6o 8 weeks is suitable, depending on clinical outcome and theresence of extravertebral extension (2,10,12,14,20). These of oral fluoroquinolones and rifampicin may providearly efficacious oral therapy (35).

MRI seems to be useful for monitoring the course of theisease and response to treatment (18,34,36,45-52). How-ver, it is important to bear in mind that signal and enhance-ent changes in MRI can persist after the clinical resolution

f the infection and gradually decrease over weeks to months42,45,46,52). This illustrates the fact that contrast enhance-ent does not always indicate active infection.The overall prognosis of PFJI is good, with a mortality rate

f 2%. Usually, patients are cured without functional se-uelae or with only residual pain, which did not impede anctive life. Of interest, after appropriate medical therapy, re-apse seems to be an exceptional event.

eferences1. David-Chausse J, Dehais J, Boyer M, Darde M, Imbert Y. Les infections

articulaires che l’adulte atteintes peripheriques et vertebrales a germesbanals et a bacilles tuberculeux. Rev Rhum 1981;48:69-76.

2. Halpin DS, Gibson RD. Septic arthritis of a lumbar facet joint. J BoneJoint Surg Br 1987;69:457-9.

3. Bellen P, Maldague B, Zech F. Arthrite septique d’une articulation in-terapophysaire vertébrale posterieure: à propos d’une cas. Rev ChirOrthop Reparatrice Appar Mot 1987;73:289-91.

4. Roberts W. Pyogenic vertebral osteomyelitis of a lumbar facet joint withassociated epidural abscess: a case report with review of the literature.Spine 1988;13:948-52.

5. Swayne LC, Dorsky S, Caruana V, Kaplan IL. Septic arthritis of a lumbarfacet joint: detection with bone SPECT imaging. J Nucl Med 1989;30:1408-11.

6. Ehara S, Khurana JS, Kattapuram SV. Pyogenic vertebral osteomyelitisof the posterior elements. Skeletal Radiol 1989;18:175-8.

7. Rousselin B, Gires F, Vallée C, Chevrot A. Case report 627: septicarthritis of lumbar facet joint as initial manifestation of spondylodisci-tis. Skeletal Radiol 1990;19:453-5.

8. Halla JT, Bliznak J, Hardin J, Finn S. Septic arthritis of the C1-C2 lateralfacet joint and torticollis: pseudo-Grisel’s syndrome. Arthritis Rheum1991;34:84-8.

9. Chevalier X, Marty M, Larget-Piet B. Klebsiella pneumoniae septic ar-thritis of a lumbar facet joint. J Rheumatol 1992;19:1817-9.

0. Peris P, Brancos MA, Gratacós J, Moreno A, Miró JM, Muñoz J. Septic

arthritis of spinal apophyseal joint. Spine 1992;17:1514-6.
Page 12: Spontaneous Pyogenic Facet Joint Infection

1

1

1

1

1

1

1

1

1

2

2

2

2

2

2

2

2

2

2

3

3

3

3

3

3

3

3

3

3

4

4

4

4

4

44

4

4

4

55

5

Spontaneous pyogenic facet joint infection 283

1. Daumen-Legre V, Chaine M, Chagnaud C, Lafforgue P, Schiano A,Acquaviva PC, et al. Arthrite septique interapophysaire vertebrale pos-terieure d’origine hematogene: une nouvelle observation et revue de lalittérature (abstract). Rev Rhum 1993;60:743.

2. Dauwe DM, Van Oyen JJ, Samson IR, Hoogmartens MJ. Septic arthritisof a lumbar facet joint and a sternoclavicular joint. Spine 1995;20:1304-6.

3. Heenan SD, Britton J. Septic arthritis in a lumbar facet joint: a rare causeof epidural abscess. Neuroradiology 1995;37:462-4.

4. Douvrin F, Callonnec F, Proust F, Janvresse A, Simonet J, Thiebot J.Arthrite septique interapophysaire lombaire: a propos de 3 cas. J Neu-roradiol 1996;23:234-40.

5. Ergan M, Macro M, Benhamou CL, Vandermarcq P, Colin T,L=Hirondel JL, et al. Septic arthritis of lumbar facet joints. A review ofsix cases. Rev Rhum Engl Ed 1997;64:386-95.

6. Ben Hamouda M, Rajhi H, Golli M, Bergaoui N, Chaouch A, Hassine H,et al. Arthrite septique interapophysaire postérieure lombaire. J Radiol1997;78:373-6.

7. Baltz MS, Tate DE, Glaser JA. Lumbar facet joint infection associatedwith epidural and paraspinal abscess. Clin Orthop 1997;339:109-12.

8. Fujiwara A, Tamai K, Yamato M, Yoshida H, Saotome K. Septic arthritisof a lumbar facet joint: report of a case with early MRI findings. J SpinalDisord 1998;11:452-3.

9. Louie T, Morgan B, Standiford HC. Facet and facet-joint infections: casereport and review. Clin Infect Dis 1998;26:510-2.

0. Cook NJ, Hanrahan P, Song S. Paraspinal abscess following facet jointinjection. Clin Rheumatol 1999;18:52-3.

1. Dayer MJ, Gransden W, Goldsmith DJ. Facet joint osteomyelitis in apatient on long-term hemodialysis. Am J Kidney Dis 2000;36:1041-4.

2. Hickey NA, White PG. Septic arthritis of a lumbar facet joint causingmultiple abscesses. Clin Radiol 2000;55:481-3.

3. Magee M, Kannangara S, Dennien B, Lonergan R, Emmett L, Van derWall H. Paraspinal abscess complicating facet joint injection. Clin NuclMed 2000;25:71-3.

4. Pilleul F, Garcia J. Septic arthritis of the spine facet joint: early positivediagnosis on magnetic resonance imaging. A review of two cases. RevRhum Fr Ed 2000;67:237-40.

5. Rombauts PA, Linden PM, Buyse AJ, Snoecx MP, Lysens RJ, GryspeerdtSS. Septic arthritis of a lumbar facet joint caused by Staphylococcusaureus. Spine 2000;25:1736-8.

6. Ishibe M, Inoue M, Saitou K. Septic arthritis of a lumbar facet joint dueto pyonex. Arch Orthop Trauma Surg 2001;121:90-2.

7. Derouet N, Haettich B, Temmar Z, Dugard D, Puechal X. Septic arthri-tis of a lumbar facet joint. A case report. Ann Med Interne (Paris)2001;152:279-82.

8. Glaser JA, El-Khoury GY. Unknown case; diagnosis: facet joint septicarthritis T12-L1 on the left with extension of the infection into thespinal canal producing a large epidural abscess. Spine 2001;26:991-2.

9. Marson F, Cognard C, Guillem P, Sévely A, Manelfe C. Septic arthritisof a lumbar facet joint associated with epidural and paravertebral softtissue abscess. J Radiol 2001;82:63-6.

0. Muffoletto AJ, Ketonen LM, Mader JT, Crow WN, Hadjipavlou AG.Hematogenous pyogenic facet joint infection. Spine 2001;26:1570-6.

1. Coscia MF, Trammell TR. Pyogenic lumbar facet joint arthritis with

intradural extension: a case report. J Spinal Disord Tech2002;15:526-8.

2. Okazaki K, Sasaki K, Matsuda S, Yuge I, Omiya K, Kido H, et al.Pyogenic arthritis of a lumbar facet joint. Am J Orthop 2002;29:222-4.

3. Orpen NM, Birch NC. Delayed presentation of septic arthritis of alumbar facet joint after diagnostic facet joint injection. J Spinal DisordTech 2003;16:285-7.

4. Doita M, Nishida K, Miyamoto H, Yoshiya S, Kurosaka M, NabeshimaY. Septic arthritis of bilateral lumbar facet joints. Report of a case withMRI findings in the early stage. Spine 2003;28:E198-E202.

5. Nolla JM, Ariza J, Gómez Vaquero C, Fiter J, Bermejo J, Valverde J, et al.Spontaneous pyogenic vertebral osteomyelitis in nondrug users. SeminArthritis Rheum 2002;31:271-8.

6. Sapico FL, Montgomerie JZ. Vertebral osteomyelitis. Infect Dis ClinNorth Am 1990;4:539-50.

7. Guri JP. Pyogenic osteomyelitis of the spine: differential diagnosisthrough clinical and roentgenographic observations. J Bone Joint Surg1946;28:29–9.

8. Liebergall M, Chaimsky G, Lowe J, Robin GC, Floman Y. Pyogenicvertebral osteomyelitis with paralysis: prognosis and treatment. ClinOrthop 1991;269:142-50.

9. Perronne C, Saba J, Behloul Z, Salmon-Ceron D, Leport C, Vilde JL, etal. Pyogenic and tuberculous spondylodiskytis (vertebral osteomyeli-tis) in 80 adult patients. Clin Infect Dis 1994;19:746-50.

0. Carragee EJ. Pyogenic vertebral osteomyelitis. J Bone Joint Surg Am1997;79:874-80.

1. Colmenero JD, Jimenez Mejías ME, Sánchez Lora FJ, Reguera JM, Pal-omino Nicás J, Martos F, et al. Pyogenic, tuberculous, and brucellarosteomyelitis: a descriptive and comparative study of 219 cases. AnnRheum Dis 1997;56:709-15.

2. Belzunegui J, Del Val N, Intxausti JJ, De Rios JR, Queiro R, González C,et al. Vertebral osteomyelitis in northern Spain. Report of 62 cases. ClinExp Rheumatol 1999;17:447-52.

3. Sapico FL. Microbiology and antimicrobial therapy of spinal infections.Orthop Clin North Am 1996;27:9-13.

4. Tay BK, Deckey J, Hu SS. Spinal infections. J Am Acad Orthop Surg2002;10:188-97.

5. Tali ET. Spinal infections. Eur J Radiol 2004;50:120-33.6. Ledermann HP, Schweitzer ME, Morrison WB, Carrino JA. MR imaging

findings in spinal infections: rules or myths? Radiology 2003;228:506-14.

7. Osenbach RK, Hitchon PW, Menezes AH. Diagnosis and managementof pyogenic osteomyelitis in adults. Surg Neurol 1990;33:266-75.

8. Stabler A, Reiser MF. Imaging of spinal infection. Radiol Clin North Am2001;39:115-35.

9. Meyers SP, Wiener SN. Diagnosis of hematogenous pyogenic vertebralosteomyelitis by magnetic resonance imaging. Arch Inter Med 1991;151:683-7.

0. Lew DP, Waldvogel FA. Osteomyelitis. Lancet 2004;364:369-79.1. Dagirmanjian A, Schils J, McHenry M, Modic MT. MR imaging of

vertebral osteomyelitis revisited. AJR Am J Roentgenol 1996;167:1539-43.

2. Gillams AR, Chaddha B, Carter AP. MR appearances of the temporalevolution and resolution of infectious spondylitis. Am J Roentgenol

1996;166:903-7.

Recommended