Paratesticular myositis ossificans of the spermatic cord
نویسندگان
چکیده
منابع مشابه
An unusual tumor of the spermatic cord: myositis ossificans.
OBJECTIVES Tumors of the spermatic cord and epididymis are rare, and their exact incidence is difficult to determine. Ninety percent of extra testicular tumors within the scrotum are found in the spermatic cord, where 30% is malignant (1). METHODS In this case report we present an unusual spermatic cord tumor, i.e. myositis ossificans (MO). To the best of our knowledge, MO of the spermatic co...
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Paratesticular LPS of the spermatic cord are rare tumor, accounting for about 7% of all paratesticular sarcomas [2]. Until date, about 200 cases have been reported in literature, most being reported as isolated cases; hence, the natural history and biological behavior of this rare tumor are less understood [3,4]. Most patients usually present with a slowly growing painless inguinoscrotal mass m...
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A 35-year-old man presented to the emergency department complaining of right hip pain after being struck by a car while crossing the road. His vital signs were stable, and he complained of right hip pain. He had no other comorbidity. On examination, tenderness and reduced abduction were noted in his right hip, but the gait was normal. The plain radiograph of his pelvis revealed a large, well-ci...
متن کاملCommentary: myositis ossificans.
M yositis ossificans, also known as ossifying hema-toma or heterotopic ossification, is a potentially disabling condition that most often affects the thigh and is typically associated with contact sports (e.g., football, rugby, lacrosse). The risk of myositis ossificans after a thigh contusion varies between 4% and 74%. The critical questions are: How can we identify high-risk patients? and Wha...
متن کاملMyositis ossificans progressiva.
Myositis ossificans progressiva is a rare, incurable disease causing progressive ossification of skeletal muscles leading to total immobility. We report one such case.
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ژورنال
عنوان ژورنال: BMJ Case Reports
سال: 2018
ISSN: 1757-790X
DOI: 10.1136/bcr-2017-223178