Myxoid dermatofibrosarcoma protruberans of the scrotum: A rare diagnosis in an unreported location
نویسندگان
چکیده
منابع مشابه
[Myxoid dermatofibrosarcoma protuberans in childhood].
Dermatofibrosarcoma protuberans is a locally aggressive skin tumor that affects young and middle-aged adults. A number of histological variants have been described, the myxoid type being one of the least common. Microscopically it is formed of a neoplastic growth that is located in the dermis and hypodermis and has a predominant myxoid component. Peripherally there are infiltrating bundles of s...
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Dermatofibrosarcoma protuberans (DFSP) is a slowly growing dermal spindle cell tumor and its myxoid variant, a rare type of DFSP, is characterized by extensive myxoid degeneration. We present the case of a 69-year-old woman with a multinodular reddish plaque on her trunk. Histopathologically, the tumor was located in the dermis and consisted of uniform spindle-shaped cells, showing strongly pos...
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Leiomyomas are benign tumors that originate from smooth muscle cells. Leiomyomas are well known to be the commonest neoplasm arising from the uterus but leiomyomas originating from the scrotum is a rare entity. They originate from the subcutaneous tissue or tunica dartos and can be solitary or multiple. We present a case of solitary scrotal leiomyoma in a 75 years old male who presented with a ...
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Figure 1. Advanced dermatofibrosarcoma protuberans of the abdominal wall. Preoperative photographs demonstrate the significance of the lesion, with the supine position being the most impressive to appreciate the fungating and necrotic nature of the mass.
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Myxoid neurofibroma (MN) is a benign tumor of the peripheral nerves arising from connective tissue cells. This is a rare tumor characterized by immunostaining for S-100 protein [1]. From its nervous origin, its topography is fairly diverse. The most common locations of the MN are the face, shoulders, arms, periungual and in the feet. Mediastinal location has not yet been described. Through obse...
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ژورنال
عنوان ژورنال: Human Pathology: Case Reports
سال: 2016
ISSN: 2214-3300
DOI: 10.1016/j.ehpc.2016.01.001