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126 bactericidal and kills bacilli which are intracellular, making glands less likely to become fluctuant on treatment. McCarthy and Rudd" in a retrospective series during 1981-85 reported successful treatment in 40 out of 41 patients treated with regime III. Dutt et al." found rifampicin and isoniazid daily for 1 month, followed by twice weekly for 8 months, a satisfactory regime for non-pulmonary tuber- culosis in 350 patients with sensitive organisms, 14 of whom had lymph node disease. The Indian study in children? showed a 98% cure rate at the end of 3 years, using an intermittent regime of thrice weekly supervised isoniazid, rifampicin, pyrazinamide and streptomycin for 2 months, followed by twice weekly streptomycin and isoniazid for 4 months. The regime was well tolerated and drug toxicity requiring interruption or alteration of treatment occurred in only 7.3% of the patients. Most of the children in this study had multiple lymph node involvement with 41% having four or more groups of nodes affected. The results of the previous studies 3 ,4,? as well as the present one have shown that lymph nodes may enlarge and new nodes may appear during and after chemotherapy. These nodes may show histological features characteristic of tuber- culosis but are sterile on culture. It is possible that the development of new nodes in these cases represents an immunological response to the tubercular protein." Surgical excision of these lymph nodes is not necessary even if they enlarge after treatment because this is usually transient. Surgery is now rarely indicated except for diagnosis and for draining of lymph node abscesses in a few patients," or for obtaining cosmetically acceptable scars. Total surgical excision of tuberculous nodes followed by chemotherapy has no advantage over simple chemotherapy. 8 The small number of events during the follow up period Ultrasonographic diagnosis of acute alcoholic hepatitis Sumino Y, Kravetz D, Kanel GC, McHutchison JG, Reynolds TB (Division of Gastrointestinal and Liver Diseases and Department of Pathology, School of Medicine, University of Southern California, Los Angeles, California, USA.) Ultrasonographic diagnosis of acute alcoholic hepatitis 'pseudoparallel channel sign' of intrahepatic artery dilatation. Gastroenterology 1993;105:1477-82. SUMMARY Using ultrasonography the authors diagnosed acute alcoholic hepatitis (AAH) by the presence of parallel tubular structures within the liver subsegments. Pulse doppler flowmetry showed that these structures were formed by a dilated branch of the hepatic artery and an adjacent branch of the portal vein. They called this the 'pseudoparallel channel sign' (PPCS). The ppes was then specifically sought by two physician operators in THE NATIONAL MEDICAL JOURNAL OF INDIA VOL. 7, NO.3, 1994 confirms the advice given by the Joint Tuberculosis Committee? that patients can be discharged after completion of the treatment, but should be reassessed if new symptoms develop. This study confirms the efficacy of the 6-month regime>? and since it is as effective as 9 months of treatment with regimes I and II, it can be recommended for routine use in patients with sensitive organisms. It is convenient, cheap and will probably improve compliance. REFERENCES British Thoracic Society. A controlled trial of six months' chemotherapy for pulmonary tuberculosis. Final report: Results during the 36 months after the end of chemotherapy and beyond. Br I Dis Chest 1984;78:330-<i. 2 Campbell lA, Dyson AJ. Lymph node tuberculosis: A comparison of treat- ments 18 months after completion of chemotherapy. Tubercle 1979;60:95-8. 3 British Thoracic Society Research Committee. Short course chemotherapy for tuberculosis of lymph nodes: A controlled trial. 8M] 1985;290: 1106-8. 4 British Thoracic Society Research Committee. Six months versus nine months chemotherapy for tuberculosis of lymph nodes: Preliminary results. Respir Med 1992;86:15-19. . 5 McCarthy OR, Rudd RM. Six months chemotherapy for lymph node tuber- culosis. Respir Med 1989;83:425-7. 6 Dutt AK, Moers D, Stead WW. Short-course chemotherapy for extrapulmonary tuberculosis. Nine years experience.Ann Intern Med 1986;104:7-12. 7 Jawahar MS, Sivasubramanian S, Vijayan VK, Ramakrishnan CV, Paramasivan CN, Selvakumar V, et 01. Short course chemotherapy for tuber- culous lymphadenitis in children. 8M] 1990;301:359--62. 8 Nanda BP, Pandhi NC, Dandapat Me. Peripheral lymph node tuberculosis-A comparison of various methods of managenient. Indian] Tuberculosis 1986; 33:20--3. 9 Ormerod LP for the Joint Tuberculosis Committee. Chemotherapy and management of tuberculosis in the United Kingdom: Recommendations of the Joint Tuberculosis Committee of British Thoracic Society. Thorax 1990;45:403-8. S. GAUDE GAJANAN 1. N. Medical College Belgaum Karnataka 77 AAH patients, 119 with other alcoholic liver diseases and 49 with non-alcoholic liver disease and 15 healthy volunteers. All patients with non-alcoholic liver disease underwent liver biopsy. Of the patients with alcoholic liver disease histological evidence was available in only 51-it was not done in the others usually because their prothrombin levels were low. ppes was seen in 90% of patients with AAH and in 23% of patients with other alcoholic liver disease. This sign was not detected in those with non-alcoholic liver disease or healthy subjects. In 51 histologically proved cases of alcoholic liver disease, ppes had a sensitivity of 82% , a specificity of 87% and an accuracy of 84% in diagnosing AAH, whereas clinical criteria correctly predicted AAH with a sensitivity of 64%, a specificity of 87% and an accuracy of 75%. Histological criteria for the diagnosis of AAH were the presence of alcoholic hyaline bodies, hepatocyte swelling, and hydropic change; focal hepatocyte necrosis and polymorphonuclear cell infiltration, and intrasinusoidal and pericentral collagen deposition. Patients with AAH had more segments involved with ppes than those who did not have AAH. PPCS was most often seen in segments 2 and 3. However, it was also found in the other segments. The authors thereby concluded that ppes might be an important diagnostic finding inAAH.
Transcript
Page 1: et al. - archive.nmji.inarchive.nmji.in/approval/archive/Volume-7/issue-3/selected-summaries-3.pdfReynolds TB (Division of Gastrointestinal and Liver Diseases and Department of Pathology,

126

bactericidal and kills bacilli which are intracellular, makingglands less likely to become fluctuant on treatment.

McCarthy and Rudd" in a retrospective series during1981-85 reported successful treatment in 40 out of 41 patientstreated with regime III. Dutt et al." found rifampicin andisoniazid daily for 1 month, followed by twice weekly for8 months, a satisfactory regime for non-pulmonary tuber-culosis in 350 patients with sensitive organisms, 14 of whomhad lymph node disease. The Indian study in children?showed a 98% cure rate at the end of 3 years, using anintermittent regime of thrice weekly supervised isoniazid,rifampicin, pyrazinamide and streptomycin for 2 months,followed by twice weekly streptomycin and isoniazid for4 months. The regime was well tolerated and drug toxicityrequiring interruption or alteration of treatment occurred inonly 7.3% of the patients. Most of the children in this studyhad multiple lymph node involvement with 41% having fouror more groups of nodes affected.

The results of the previous studies3,4,? as well as the presentone have shown that lymph nodes may enlarge and newnodes may appear during and after chemotherapy. Thesenodes may show histological features characteristic of tuber-culosis but are sterile on culture. It is possible that thedevelopment of new nodes in these cases represents animmunological response to the tubercular protein." Surgicalexcision of these lymph nodes is not necessary even if theyenlarge after treatment because this is usually transient.Surgery is now rarely indicated except for diagnosis and fordraining of lymph node abscesses in a few patients," or forobtaining cosmetically acceptable scars.

Total surgical excision of tuberculous nodes followed bychemotherapy has no advantage over simple chemotherapy. 8

The small number of events during the follow up period

Ultrasonographic diagnosis of acute alcoholichepatitis

Sumino Y, Kravetz D, Kanel GC, McHutchison JG,Reynolds TB (Division of Gastrointestinal and LiverDiseases and Department of Pathology, School of Medicine,University of Southern California, Los Angeles, California,USA.) Ultrasonographic diagnosis of acute alcoholichepatitis 'pseudoparallel channel sign' of intrahepatic arterydilatation. Gastroenterology 1993;105:1477-82.

SUMMARYUsing ultrasonography the authors diagnosed acute alcoholichepatitis (AAH) by the presence of parallel tubular structureswithin the liver subsegments. Pulse doppler flowmetry showedthat these structures were formed by a dilated branch of thehepatic artery and an adjacent branch of the portal vein. Theycalled this the 'pseudoparallel channel sign' (PPCS). The ppeswas then specifically sought by two physician operators in

THE NATIONAL MEDICAL JOURNAL OF INDIA VOL. 7, NO.3, 1994

confirms the advice given by the Joint TuberculosisCommittee? that patients can be discharged after completionof the treatment, but should be reassessed if new symptomsdevelop. This study confirms the efficacy of the 6-monthregime>? and since it is as effective as 9 months of treatmentwith regimes I and II, it can be recommended for routine usein patients with sensitive organisms. It is convenient, cheapand will probably improve compliance.

REFERENCESBritish Thoracic Society. A controlled trial of six months' chemotherapy forpulmonary tuberculosis. Final report: Results during the 36 months after theend of chemotherapy and beyond. Br I Dis Chest 1984;78:330-<i.

2 Campbell lA, Dyson AJ. Lymph node tuberculosis: A comparison of treat-ments 18 months after completion of chemotherapy. Tubercle 1979;60:95-8.

3 British Thoracic Society Research Committee. Short course chemotherapy fortuberculosis of lymph nodes: A controlled trial. 8M] 1985;290: 1106-8.

4 British Thoracic Society Research Committee. Six months versus nine monthschemotherapy for tuberculosis of lymph nodes: Preliminary results. Respir Med1992;86:15-19. .

5 McCarthy OR, Rudd RM. Six months chemotherapy for lymph node tuber-culosis. Respir Med 1989;83:425-7.

6 Dutt AK, Moers D, Stead WW. Short-course chemotherapy for extrapulmonarytuberculosis. Nine years experience.Ann Intern Med 1986;104:7-12.

7 Jawahar MS, Sivasubramanian S, Vijayan VK, Ramakrishnan CV,Paramasivan CN, Selvakumar V, et 01. Short course chemotherapy for tuber-culous lymphadenitis in children. 8M] 1990;301:359--62.

8 Nanda BP, Pandhi NC, Dandapat Me. Peripheral lymph node tuberculosis-Acomparison of various methods of managenient. Indian] Tuberculosis 1986;33:20--3.

9 Ormerod LP for the Joint Tuberculosis Committee. Chemotherapy andmanagement of tuberculosis in the United Kingdom: Recommendations of theJoint Tuberculosis Committee of British Thoracic Society. Thorax 1990;45:403-8.

S. GAUDE GAJANAN1. N. Medical College

BelgaumKarnataka

77 AAH patients, 119 with other alcoholic liver diseases and49 with non-alcoholic liver disease and 15 healthy volunteers.All patients with non-alcoholic liver disease underwent liverbiopsy. Of the patients with alcoholic liver disease histologicalevidence was available in only 51-it was not done in the othersusually because their prothrombin levels were low. ppes wasseen in 90% of patients with AAH and in 23% of patients withother alcoholic liver disease. This sign was not detected in thosewith non-alcoholic liver disease or healthy subjects. In 51histologically proved cases of alcoholic liver disease, ppes hada sensitivity of 82% , a specificity of 87% and an accuracy of 84%in diagnosing AAH, whereas clinical criteria correctly predictedAAH with a sensitivity of 64%, a specificity of 87% and anaccuracy of 75%. Histological criteria for the diagnosis ofAAH were the presence of alcoholic hyaline bodies, hepatocyteswelling, and hydropic change; focal hepatocyte necrosis andpolymorphonuclear cell infiltration, and intrasinusoidal andpericentral collagen deposition. Patients with AAH had moresegments involved with ppes than those who did not haveAAH. PPCS was most often seen in segments 2 and 3. However,it was also found in the other segments. The authors therebyconcluded that ppes might be an important diagnostic findinginAAH.

Page 2: et al. - archive.nmji.inarchive.nmji.in/approval/archive/Volume-7/issue-3/selected-summaries-3.pdfReynolds TB (Division of Gastrointestinal and Liver Diseases and Department of Pathology,

SELECTED SUMMARIES

COMMENTWith the increasing consumption of alcohol in India a non-invasive test to diagnose AAH would be helpful. AAH isusually diagnosed by clinical features such as jaundice, aserum aspartate aminotransferase (AST) level greater thanthe alanine aminotransferase (ALT) level,' a marked re-distribution of isotope on a 99mTc-sulphur colloid liver andspleen scan, and at least three of the following: tenderhepatomegaly, fever (37.5 "C), leucocytosis (10000 percmm) and a systolic hepatic bruit. However, it may,sometimes, be difficult to diagnose in patients with atypicalclinical characteristics. It is in this subset of patients that thepresence of PPCS on ultrasonography would have clinicalrelevance.

There is an increase in hepatic blood flow in patients withAAH and PPCS represents hepatic arterial dilatation. Thishas been shown earlier by angiography. 2,3 It is also wellknown that dilatation of the hepatic arteries and an increasedarterial flow can be seen in patients with portal hypertensionand chronic liver disease." This is, perhaps, because of theincreased number of shunts, between the hepatic arteries andportal veins in cirrhosis, which occur as a compensatingmechanism for decreased portal venous flows or because ofthe release of vasoactive substances by the liver. 6 Theauthors state that PPCS was not found in any of the 49patients with non-alcoholic liver diseases or in the 15 healthyvolunteers. They do not explain why PPCS was not seen inthe 11 patients with chronic viral hepatitis with cirrhosis and5 with primary biliary cirrhosis who have portal hypertensionin whom hepatic arterial dilatation should also be present.Perhaps alcohol per se might cause hepatic arterial dilatation.

127

PPCS should be distinguished from the 'parallel channel sign'which is seen in patients with biliary obstruction. This canbe done using either the pulse doppler flowmeter or byretrograde cholangiography. At times it may be difficult todemonstrate PPCS in all liver segments in patients with AAHin the presence of severe fatty degeneration but in themajority it is apparently easily seen. .

We feel this sign needs further evaluation and mayprovide an important non-invasive low-cost clue to thediagnosis of AAH.

REFERENCESHale P, Pare P, Kaptein E, Kanel G, Redeker AG, Reynolds TB. Double-blindcontrolled trial of propylthiouracil in patients with severe acute alcoholichepatitis. Gastroenterology 1982;82:925-31.

2 Kotelanski B, Groszmann R, Cohn IN. Circulation times in the splanchnic andhepatic beds in alcoholic liver disease. Gastroenterology 1972;63:102-11.

3 Rourke JA, Bosniak MA, Ferris EJ. Hepatic angiography in 'alcoholichepatitis'. Radiology 1968;91:2~.

4 Hales MR, Allan JS, HaUEM. Injection corrosion studies of normal and cirrhoticlivers. Am J Patho11959; 35:909-39.

5 Viamonte M Jr, Warren WD, Fomon JJ. Liver panangiography in the assess-ment of portal hypertension in liver cirrhosis. Radial c/in North Am 1970;8:147~7.

6 Richardson PDI, Withrington PG. Liver blood flow. II. Effects of drugs andhormones on liver blood flow. Gastroenterology 1981;81:356-75.

M. DWlVEDIS.P.MISRA

Department of GastroenterologyM. L. N. Medical College

AllahabadUttar Pradesh


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