+ All Categories
Home > Documents > H. Sidra yasin

H. Sidra yasin

Date post: 23-Feb-2016
Category:
Upload: aviva
View: 64 times
Download: 0 times
Share this document with a friend
Description:
H. Sidra yasin. Medical Biotechnology. Blood cancer. Pluripotent hematopoietic stem cells are common ancestral cells for all blood and immune cells. In blood cancer the blood cells produce abnormally and enormously, disturb the normal blood cells production and their normal function. - PowerPoint PPT Presentation
33
H. Sidra yasin Medical Biotechnology
Transcript
Page 1: H. Sidra yasin

H. Sidra yasin

Medical Biotechnology

Page 2: H. Sidra yasin

Blood cancer

Page 3: H. Sidra yasin

Pluripotent hematopoietic stem cells are common ancestral cells for all blood and immune cells.

Page 4: H. Sidra yasin

• In blood cancer the blood cells produce abnormally and enormously, disturb the normal blood cells production and their normal function.

Page 5: H. Sidra yasin

Types of blood cancer

• Leukemia • Lymphoma• Myeloma

The classification is according to cells which affect in a particular type of these cancers.

Page 6: H. Sidra yasin

Leukemia

• Leukemia means ‘many white cells in the blood’

Page 7: H. Sidra yasin

Types of Leukemia

• Lymphocytic– Acute– Chronic

• Myelogenous– Acute– ChronicAcute form of any disease progress rapidly and Chronic form progress slowly.

Page 8: H. Sidra yasin

Acute Lymphocytic Leukemia

• Acute Lymphoblastic Leukemia.• In ALL unusually immature white blood

cells grow quickly and replace normal, healthy blood cells and prevent the production of these.

Page 9: H. Sidra yasin

Prevalance

• It is more common type of leukemia of all blood cancers almost 25%, in children.

• Infants having ALL are 4 times and youth of 19 years old are 10 times more than children of ages of 2-3 among all children.

• It also affects adults. • There are almost 5,000 patients of ALL

appeared each other.

Page 10: H. Sidra yasin

Causes

• Exposure to radiation: Prenatal exposure to x-ray, postnatal exposure to high radiation.

• Chromosomal problems: Chromosomal translocation in the cells at the time of birth causes ALL.

• Toxins: Like benzene.• Chemotherapeutic drugs.

Page 11: H. Sidra yasin

Effects of these Environmental factors

• Formation of fusion genes• Dysregulation of proto-oncogene

Page 12: H. Sidra yasin

Genetic Disorders

• Children having Down syndrome have an increased risk for both ALL and Acute Myeloid Leukemia.

• Associated with the diseases of Neurofibromatosis, Shwachman syndrome, Bloom syndrome and Ataxia telangiectasia.

Page 13: H. Sidra yasin

Cytogenetic

• Chromosome translocation; between 9 and 22( Philadelphia chromosome, 4 and 11 in infants.

Page 14: H. Sidra yasin

Diagnosis

• Blood test• Serological tests• DNA test

Page 15: H. Sidra yasin

Symptoms• Breathlessness.• Pitting edema (swelling) in the lower limbs and abdomen.• Bone pain and joint pain because of the spread of blast cells to the

surface of bone or into the joint from the marrow cavity.• Patients of it also have easy bruising and bleeding from the different

parts of the body such as skin, gums, nose.• Fever.• Tiredness and weakness.• Less appetite and weight loss.• Petechia means tiny red spots or lines on the skin due to less in

platelets.• Swollen lymph glands (lymphadenopathy) of underarm, neck and groin.• Night sweats.

Page 16: H. Sidra yasin

Treatment• Chemotherapy: ALL can spread to the spinal cord

and brain so chemotherapeutics which are given through the vein cannot reach these parts of the body so we give chemotherapeutics directly to these areas.

• Radiotherapy: We also do radiotherapy in the brain and spinal column.

• Blood transfusion: Patient due to anaemia may need blood products transfusion like RBCs and platelets.

• Antibiotics: As patients of ALL have many infections so antibiotics are needed.

Page 17: H. Sidra yasin

Bone marrow transplantation (Stem cell transplantation)

• If patients do not respond other treatments and experience again onset of ALL then usually patients are given stem cells transplantation or bone marrow transplantation.

Major interest of biotechnologists.

Page 18: H. Sidra yasin

Prevention• There is almost no known way to prevent it. • But we should avoid unnecessary exposure

to x-rays and toxins also • We should immediately consult the doctor if

having some kind of above mentioned symptoms.

• Also the people having family history of any kind of blood cancer have to be very careful and share their family medical history with the doctors.

Page 19: H. Sidra yasin
Page 20: H. Sidra yasin

Chronic Lymphocytoic Leukemia

• This type of Leukemia progress slowly. In it also white blood cells or lymphocytes are abnormally increase.

Page 21: H. Sidra yasin

Prevalance

• It doesn't affect children.• The patients of 65 are found abundantly.• Under the age of 40 are very rare. • Common in men than women.• 15,000 new cases of CLL each year. 

Page 22: H. Sidra yasin

Risk factors

• Exposure to toluene, benzene and x-ray• Having family history of any kind of blood

cancer• Chemotherapeutic drugs• Exposure to radiation: Prenatal exposure

to x-ray, postnatal exposure to high radiation.

Page 23: H. Sidra yasin

Symptoms• Fever.• Night sweats.• Repeated infections.• Tiredness and weakness.• Weight loss and appetite.• Enlarged lymph gland (which are painless)

especially in the neck, armpit and groin.• In some patients an enlarged spleen found

and it can cause pain.

Page 24: H. Sidra yasin

Diagnosis

• Blood test• Serological tests• DNA test

Page 25: H. Sidra yasin

Treatment

• When patients become anaemic or have many enlarged lymph glands. Then treatments is necessary.

Page 26: H. Sidra yasin

• Chemotherapy:– Chlorambucil (leukerin) is usually given.– Fludarebine (Fludara) in late stage diseases.– In bone marrow failure steroid treatment

with Prednisolone (e.g., Deltacordril) – In Milder bone marrow failure repeated

blood transfusion.

Page 27: H. Sidra yasin

Radiotherapy:• To cure swollen lymph nodes. In many small

repeated doses are given to the whole body. Surgical removal:• Sometimes spleen swells so much causing pain

and anaemia. So, surgical removal of spleen becomes must.

Antibiotics: • Repeated infections.

Page 28: H. Sidra yasin

Bone marrow transplantation:

• Stem cell transplantation• In those patients who are under the age

of 45 and have severe form of CLL. Major interest of biotechnologists

Page 29: H. Sidra yasin
Page 30: H. Sidra yasin

Prevention

• As the causes of CLL is still unknown so there is no certain way to prevent it

• But avoidE the exposure to toluene benzene and x-rays

• Immediately consult the doctor • People having family history of any kind

of blood cancer have to be very careful and share their family medical history

Page 31: H. Sidra yasin

Research in Pakistan

• Individually• In collaboration with the research

institutes in Canada, Germany, U.S, ChinaASH (American Society of Hematology)AACR (American Associates for Cancer

Research)

Page 32: H. Sidra yasin

ReferencesWeb references:• www.ncbi.nlm.nih.gov/pubmedhealth• www.netdoctor.co.uk• www.medicinenet.com/leukemia/page3• www.hematology.org/patients/Blood-Disorders/Blood-Cancers/

5229.aspx• http://www.defence.pk/forums/current-events-social-issues/94389-

pakistani-scientist-s-research-leukemia-recognized-ash.htmlPrimary references:• www.medterms.com/script/main/art.asp?articlekey=13660• www.emedicine.medscape.com/article/207631-overview• http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1988840/Book reference:• Klaus D. Elgert, Immunology understanding the immune system.

Second edition; A John Wiley and Sons, Inc., Publication 2009. Page 29.

Page 33: H. Sidra yasin

You can go home now from hospital!!!


Recommended