scholarly journals Aplasia medular congénita de serie roja: Anemia de Diamond Blackfan. A propósito de un caso

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jenny Planchet ◽  
Mary Tovar ◽  
Abril Espinoza ◽  
Alba Díaz

Pure red cell aplasia medullary is a disorder characterized by anemia with almost complete absence of red cell precursors in the bone marrow, with leukocyte count and platelets. The Diamond-Blackfan anemia is a failure syndrome characterized by bone marrow anemia, reticulocytopenia and decreased erythroid precursors in the bone marrow. the case of an infant under 2 months of age presented no family or perinatal history major, whose mother progressive skin pallor evidence mucosa associated with hyporexia; go to health center where they perform paraclinical reporting hemoglobin 1.7 g / dL. peripheral blood smear where erythroid frankly affected with normal megakaryocytic granulocytic count shown is made; It biopsied and bone marrow aspirate concluding marrow red cell aplasia; possible anemia Diamond-Blackfan in light of other clinical findings arises. It stays with glucocorticoid treatment, however insufficient response, begins erythropoietin dose progressively increasing, despite it, warrants blood transfusions on a regular basis; compatibility studies performed with first-degree resulting positive, currently a candidate for allogeneic bone marrow transplantation. It is concluded that despite being a rare syndrome should be suspected in severe anemia where there is acute blood loss, ruling out other etiologies; also timely initiation of treatment is critical to the survival of these patients.

Blood ◽  
1962 ◽  
Vol 19 (2) ◽  
pp. 168-180 ◽  
Author(s):  
L. K. KHO ◽  
O. ODANG ◽  
S. THAJEB ◽  
A. H. MARKUM

Abstract Erythroblastopenia or pure red cell aplasia was encountered in 186 children during an observation period of five years in the Pediatric Department in Djakarta, Indonesia. Twenty cases were of the acute type of erythroblastopenia, distinguished by a sudden drop of the hemoglobin content of the blood, reticulocytopenia, and disappearance of the erythroblasts in the bone marrow. Giant red cell precursors (giant reticular cells and proerythroblasts) appeared in the bone marrow. This condition lasted two days to two weeks. A subacute type of erythroblastopenia with a duration of two weeks to two months was found in 25 cases. The last group consisted of 141 cases of subchronic or chronic erythroblastopenia with a duration of more than two months. Malnutrition, infections and vitamin deficiencies were the main clinical findings in these children. The authors are of the opinion that erythroblastopenia is a maturation arrest of the erythropoietic system caused by protein deficiency and/or temporary deficiencies of one or more erythrocyte maturation or stimulating factors.


2021 ◽  
pp. 55-56
Author(s):  
G Srivani ◽  
D Roja Aishwarya ◽  
P. V. S. Kiran

Pure cell aplasia is a rare bone marrow failure that affects erythroid lineage characterized by normocytic normochromic anemia with reticulocytopenia in the peripheral blood and absent or infrequent erythroblasts in the bone marrow. It can be congenital or acquired. Acquired can be primary when no cause is identied or secondary-due to underlying or associated pathology. Herein we report a case of a 28 year old female with Primary Acquired Pure Red cell aplasia. The patient presented with severe anemia (Hb-1.9gm%) and low reticulocyte count 0.1%. Bone marrow aspiration shows normocellular marrow with Decreased erythropoiesis with M:E ratio of 20:1..Patient was started on oral prednisolone and improvement was seen and the patient became transfusion independent.


Sign in / Sign up

Export Citation Format

Share Document