Hard to find and tricky to treat: A case series of acquired amegakaryocytic thrombocytopenia
Acquired amegakaryocytic thrombocytopenia (AAMT) is a rare hematological disorder characterized by prolonged, severe thrombocytopenia, and reduced megakaryocytes on otherwise normal bone marrow biopsy. We report three cases of which two ultimately responded to treatment with eltrombopag, and one who...
Saved in:
Main Authors: | Amina Anwar (Author), Zena Chahine (Author), Dava Piecoro (Author), Melissa Kesler (Author), Ayman Qasrawi (Author) |
---|---|
Format: | Book |
Published: |
Elsevier,
2023-09-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Transient acquired amegakaryocytic thrombocytopenia associated with Pediatric Hodgkin Lymphoma: A case report
by: Fatima Meraj, et al.
Published: (2021) -
Congenital amegakaryocytic thrombocytopenia- A rare case report
by: Ariba Afeeh, et al.
Published: (2024) -
Congenital Amegakaryocytic Thrombocytopenia: A Brief Review of the Literature
by: Fatma S. Al-Qahtani
Published: (2010) -
Myelodysplastic Syndrome Presenting as Amegakaryocytic Thrombocytopenia in a Collodion Baby
by: Mohammed Al Pakra MD, et al.
Published: (2015) -
Case Report: Successful Avatrombopag Treatment for Two Cases of Anti-PD-1 Antibody-Induced Acquired Amegakaryocytic Thrombocytopenia
by: Xiaofang Tu, et al.
Published: (2022)