غدير أبو شعبان تسنيم الشلفوح سجود الجبالي

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غدير أبو شعبان تسنيم الشلفوح سجود الجبالي Leukemia case study غدير أبو شعبان تسنيم الشلفوح سجود الجبالي

MDS case study: 80-year-old female with macrocytic anemia

Consultation A 80-year-old woman was referred to our institution in 2006 because of a persistent macrocytic anemia. She presented with tiredness and dizziness.

Medical history: Physical examination: No allergies. Non-smoker. • Mild vitamin B12 deficiency and macrocytic anemia diagnosed in 2005. Despite of the correct treatment with intramuscular vitamin B12, the anemia persisted. • Chronic atrophic gastritis. • Hypertension. Physical examination: skin pallor with no other significant abnormalities.

Blood tests (I): • RBC 91x109/L, Hb 7.4 g/dL, Htc 22.9%, MCV 119.9 fL, MHC 38.7pg, WBC 5.14x109/L, platelets 306x109/L. Reticulocytes: 2.59 %, total 49.5x109/L. • Glucose 120 mg/dl, Creatinine 0.99 mg/dl, LDH 329 UI/L, Bilirrubin 0.53mg/dl, AST 12 UI/L, ALT 9 UI/L, GGT 60 UI/L, AF 40 UI/L, Total proteins 6.9 g/dL, Albumin 4.4 g/L, EPO 678 mU/mL, Vitamin B12 464 pg/mL, Folic acid 10.9 ng/mL, Ferritin 126 ng/mL. • HBV, HCV, HIV negatives. • Prothrombin rate 71%, aPTT 27 seg.

Blood tests (II): • Peripheral blood smear: – WBC differential count: 64N, 4Eo, 0B, 28L, 4M. – Anisopoikilocytosis, macrocytosis, polycromasia, basophilic stippling. Some schistocytes, elliptocytes and dacryocytes. – Anisocytosis of platelets. – Doble population of neutrophils: coexistence of normal and marked hypogranulated elements.

Bone marrow aspirate: Hypercellular. Megakaryopoiesis: abundant. 58% of dysmorphic elements: small megakaryocytes with hypo- or monolobated nucleus. Erythropoiesis: 15%. Asynchronic maduration, nuclear budding, altered mitosis, irregular distribution of hemoglobin and presence of Höwell-Jolly bodies. Granulopoiesis: 61%. Hypogranulated neutrophils with Döhle bodies. 6% blasts (3% type I and 3% type II). Mononuclear phagocytic system : 3%. Lymphocytes:19%. Plasma cells: 2% Normal macrophagic iron store. Sideroblasts type I and II: 48%. No ring sideroblasts.