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[Extra medullary hematopoiesis associated to congenital dyserythropoietic anemia II in adult].

Authors :
Jedidi I
Medhaffar M
Ghorbel M
Hdiji S
Makni F
Elloumi M
Kallel C
Source :
Annales de biologie clinique [Ann Biol Clin (Paris)] 2012 Mar-Apr; Vol. 70 (2), pp. 217-20.
Publication Year :
2012

Abstract

The congenital dyserythropoietic anemias comprise a group of rare hereditary disorders of erythropoiesis characterized by anemia with ineffective erythropoiesis and morphological abnormalities of erythroblasts in the bone marrow. Congenital dyserythropoietic anemia type II or HEMPAS is the more frequent type. It is rare in adults. Extra medullary hematopoiesis is also a rare entity; it is a physiological response to chronic anemia observed in certain hemopathies like congenital dyserythropoietic anemia type II. We report the observation of a patient for who diagnosis of extra medullary hematopoiesis associated to congenital dyserythropoietic type II was made in adulthood.

Details

Language :
French
ISSN :
0003-3898
Volume :
70
Issue :
2
Database :
MEDLINE
Journal :
Annales de biologie clinique
Publication Type :
Academic Journal
Accession number :
22484535
Full Text :
https://doi.org/10.1684/abc.2012.0694