Un purpura thrombopénique amégacaryocytaire acquis qui cache une leucémie aigue myéloblastique

Acquired amegakaryocytic thrombocytopenic purpura is a very rare condition characterized by severe thrombocytopenia linked to the reduction or disappearance of megakaryocytes in the bone marrow. It may be primary idiopathic or secondary to many pathological conditions including hematologic disorders...

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Podrobná bibliografie
Vydáno v:Pan Afr Med J
Hlavní autoři: Eddou, Hicham, Zinebi, Ali, Khalloufi, Abdelaziz, Sina, Mohammed, Mahtat, Mehdi, Doghmi, Kamal, Mikdame, Mohammed, Moudden, Mohammed Karim, Baaj, Mohammed El
Médium: Artigo
Jazyk:Inglês
Vydáno: The African Field Epidemiology Network 2017
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5398219/
https://ncbi.nlm.nih.gov/pubmed/28451010
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.26.32.9215
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