Hemophilic Pseudotumor of Humerus in an Adolescent with Severe Hemophilia A

Mohammadi Moghaddam, Soha; Khalili, Mitra; Habibpanah, Behnaz

Volume 13, Issue 4 ( December 2021 2021) Iranian Journal of Blood and Cancer 2021, 13(4): 149-150 | Back to browse issues page

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Mohammadi Moghaddam S, Khalili M, Habibpanah B. Hemophilic Pseudotumor of Humerus in an Adolescent with Severe Hemophilia A. Iranian Journal of Blood and Cancer 2021; 13 (4) :149-150
URL: http://ijbc.ir/article-1-1230-en.html

Hemophilic Pseudotumor of Humerus in an Adolescent with Severe Hemophilia A

Soha Mohammadi Moghaddam¹

, Mitra Khalili ^*

², Behnaz Habibpanah¹

1- Pediatric Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
2- Pediatric Radiology Department, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Abstract: (1375 Views)

Repeated bleeding into the joints often occurs in the first decade of life in patients with hemophilia. Joint degeneration is progressive, and although early treatment can slow the process, destruction of the joint is unavoidable. Hemophilic pseudotumors (HPT) are developed due to recurrent bleeding from extra-articular bone or soft tissues.

Keywords: Hemophilic Pseudotumor, Severe Hemophilia A

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: Special Issue | Subject: Adults Hematology & Oncology
Received: 2022/02/13 | Accepted: 2021/12/10 | Published: 2022/02/13

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