Aplastic anemia

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APLASTIC ANEMIA

Transcript of Aplastic anemia

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APLASTIC ANEMIA

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CONTENTS

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INTRODUCTION

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Figure 1:Bone Marrow

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CAUSES

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Figure 2:Epstein Barr virus Figure 3: Parovirus

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STATISTICS

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SYMPTOMS

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Figure 4:Red spots Figure 5:Bruise

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LAB DIAGNOSIS1. Complete blood count (CBC)

(a) low RBC, WBC, platelets

(b) low Hb and Ht level

2. Reticulocyte count

COMPONENT NORMAL VALUE

MALE FEMALE

RBC 4.7 – 6.1 mil cell/mcL 4.2 – 5.4 mil cell/mcL

Hemoglobin 13.8 – 17.2 gm/dL 12.1 – 15.1 gm/dL

Hematocrit 40.7 – 50.3 36.1 – 44.3

WBC 4500 – 10 000 cell/mcL

Platelet 150 000 - 400 000 /mcL

Reticulocyte 0.5 – 1.5%

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3. Bone marrow test (a) BM aspiration (fluid) (b) BM biopsy (tissue)

4. Antibody test

5. Other test a) Vitamin B12 & folate test b) Liver test & viral test c) X-ray, CT scan d) ultrasound imaging test

Figure 6: BM Biopsy

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TREATMENT

1. Stem cell transplant

2. Immunosuppressant

3. Blood transfusion

4. Bone marrow stimulant

5. Antibiotics & antiviral

Figure 7:Blood transfusion

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PREVENTION

Avoid exposure to:

a) Insecticide

b) Herbicides

c) Organic solvents

d) Toxic chemical

Figure 8: Exposure to herbicides

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CONCLUSION

Aplastic anemia - blood disorder that can be inherited or acquired

Serious problem - no enough oxygen supply in body - infection

Treatment - medications, stem cell transplant & blood transfusion

Patients are advised to:

a)Take good rest when neededb)Avoid contact sportsc)Be hygienic

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CASE STUDY

1. Patient’s Detail

46 years old male Hepatitis C virus (HCV) infection Combination treatment of PEG-IFN-a 2a (180 μg, weekly) and

ribavirin (1200 mg/day) was commenced for a period of 48 weeks

2. Symptoms

Bleeding tendency Unexplained fatigue of recent onset

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3. Physical Examination

Generalized purpura and bruising, pallor of the skin and mucous membranes

The patient’s liver, spleen and lymph nodes- not enlarged

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Figure 9: A bone marrow biopsy showing the absence of hematopoietic tissue and its replacement with fat.

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4. TREATMENT

Allogeneic bone marrow transplantation after completing two courses of immunosuppressive.

Therapy with antithymocyte globulin and cyclosporin A.

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REFERENCES Anonymous, (2012), What is aplastic anemia, Viewed on 8thth

February 2013, http://www.mayoclinic.com/health/risk -factors Anonymous, (2012), Diagnosis of aplastic anemia, Viewed on 8thth

February 2013, http://www.nhlbi.nih.gov/health-topics.html Anonymous, (2013), Aplastic anemia-info, Viewed on 8thth February

2013, http://www.bodyandhealth.canada.com Anonymous, (2005), Causes of aplastic anemia, Viewed on 8thth

February 2013, http://www.childrenhospital.org David C., (2012), Idiopathic-aplastic anemia, Viewed on 8thth

February 2013, http://www.health.nytimes.com/health/guides.html

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Anonymous, (2008), Aplastic anemia, Viewed on 8thth February 2013, http://www.uth.tmc.edu/pathology/medic.html

Anonymous, (2012), Statistics of aplastic anemia, Viewed on 8thth

February 2013, http://www.aamds.org Anonymous, (2012), diagnosis, viewed on 8th February 2013,

http://www.nhlbi.nih.gov/health/health-topics/topics/aplastic/ Anonymous, (2013), bone marrow biopsy, prevention, viewed on 8th

February 2013, http://www.mayoclinic.com/health/medical/IM01819 Anonymous, (2011), CBC, viewed on 8th February 2013,

http://www.aamds.org/about/blood-and-bone-marrow-basics/CBC

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Anonymous, (2013), treatment, prevention, viewed on 8th February

2013, http://www.mayoclinic.com/health/aplastic-anemia/DS00322 Anonymous, (2011), treatment, viewed on 8th February 2013,

http://www.aamds.org/about/aplastic-anemia

Ioannou, S., Hatzis, G., Vlahadami, I., Voulgarelis, M.(2010),Aplastic anemia associated with interferon alpha 2a in a patient with chronic hepatitis C virus infection: a case report. J Med Case Rep. 4(268)

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