Hemophilic Pseudotumor of Humerus in an Adolescent with Severe Hemophilia A

نویسندگان
Mohammadi Moghaddam, Soha ID 1
Khalili, Mitra ID 2
Habibpanah, Behnaz ID 3

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

3 Pediatric Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran

doi
چکیده

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.

کلیدواژه‌ها
Hemophilic Pseudotumor, Severe Hemophilia A