THE HAEMOPHILIC PSEUDOTUMOUR OR HAEMOPHILIC SUBPERIOSTEAL HAEMATOMA
نویسندگان
چکیده
منابع مشابه
Synovial Sarcoma Mimicking Haemophilic Pseudotumour
This is a case of a 36-year-old gentleman with haemophilia A who was presented with an acute atraumatic soft tissue swelling in the right thigh. Open biopsy was performed with the resultant diagnosis of a synovial cell sarcoma. Although the clinical findings were nonspecific they could easily have been found in a bleeding haemophilic pseudotumour. The findings reported on MRI scan initially wer...
متن کاملPelvic haemophilic pseudotumour: a case report.
We report on a 30-year-old haemophilic man with a pelvic pseudotumour compressing adjacent structures causing pain and swelling and destruction of surrounding soft tissues and bones. He underwent evacuation of the pseudotumour, acetabular reconstruction using the Harrington procedure, and total hip arthroplasty.
متن کاملLong-term outcome of an unusual haemophilic pseudotumour.
Haemophilia, a lifelong congenital bleeding disease, is a highly demanding disorder, due to the costs of its replacement therapy. In the absence of this pivotal treatment, life expectancy and quality of life are deleteriously affected. As illustration, we present a 14 years long follow-up of a patient with severe haemophilia A, treated sporadically with fresh plasma, cryoprecipitate and factor ...
متن کاملPelvic haemophilic pseudotumour in a patient with haemophilia.
To cite: Samanci C, Ayvaci A, Korkmaz O, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2013-008731 DESCRIPTION We report a 20-year-old male patient, with a history of haemophilia presented with a sudden onset of pain in the right gluteal region of 5 days duration. He is afebrile; there is no history of trauma. He developed painful swelling in his right g...
متن کاملHaemophilic arthropathy.
Haemophilia is a heredity disorder in which bleeding is due to deficiency of coagulation factor VIII. Haemophilia A is the second most common inherited coagulation disorder. Estimation of its incidence ranges from 1 in 20,000 to as high as 1 in 10,000 people. It is a classic example of x-linked recessive trait (1). The frequency and severity generally are related to the blood level of factor VI...
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ژورنال
عنوان ژورنال: The Journal of Bone and Joint Surgery. British volume
سال: 1965
ISSN: 0301-620X,2044-5377
DOI: 10.1302/0301-620x.47b2.256