Hard to find and tricky to treat: A case series of acquired amegakaryocytic thrombocytopenia
Human Pathology Reports(2023)
摘要
•AAMT is a rare disorder characterized by severe thrombocytopenia.•Reduced megakaryocytes on otherwise normal bone marrow biopsy is expected in AAMT.•Diagnosis is difficult, often mistaken for ITP.•There are currently no standard treatment guidelines for AAMT.
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case series
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