Dysmegakaryopoiesis, a clue for an early diagnosis of familial platelet disorder with propensity to acute myeloid leukemia in case of unexplained inherited thrombocytopenia associated with normal-sized platelets.

Date publication

octobre 2011

Auteurs

Membres identifiés du Cancéropôle Est :
Pr PHILIPPE Christophe

Tous les auteurs :
Latger-Cannard V, Philippe C, Jonveaux P, Lecompte T, Favier R

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/21900832

Résumé

We report dysmegakaryopoiesis in a case of familial platelet disorder with predisposition to acute myeloid leukemia (familial platelet disorder/acute myeloid leukemia phenotype Mendelian Inheritance in Man number 601 399). Slight reduction of the number of megakaryocytes with high nucleocytoplasmic ratio, strongly basophilic cytoplasm and poorly lobulated nuclei are suggestive of megakaryocytic dysplasia.

Référence

J Pediatr Hematol Oncol. 2011 Oct;33(7):e264-6.