منابع مشابه
A Case Report of Aggressive Metastatic Parachordoma
Parachordoma, first described by Laskowski in 1951, is a rare tumor of soft tissue. Few than 100 cases have been reported in the literature. In 1977 Dabska M. collected 10 cases of parachordoma and he described it as a slow growing, locally invasive tumor.1 Since then, metastatic cases have been described but they are also so rare. In this report, we present a case of parachordoma with an agres...
متن کاملClinical and radiological presentations of pelvic parachordoma
Parachordoma is an extremely rare entity and there are only about 50 to 60 cases reported, in which there is only one definite pelvic parachordoma. We present a huge well-defined presacral tumor in a 48-year-old woman who has the symptoms of lower abdominal pain and difficulty in defecating. Radiological findings of the tumor on computed tomography and magnetic resonance imaging are described i...
متن کاملParachordoma of the Chest Wall: Case Report
with unique immuno-histochemical features, and it can arise from the arm, thigh, leg, chest wall, and buttock (1-6). The histogenesis of parachordoma is still controversial. These tumors display a slow growing nature, but they also show locally destructive growth. After surgery, local recurrence has been reported in some cases (1, 2). We report the imaging features of histologically confirmed p...
متن کاملParachordoma: a recurrent case and review of the literature.
Parachordoma is an uncommon tumor of soft tissue, and the origin is not clear. Recurrence and metastasis are rarely seen. A piecemeal mass measuring 7x4x3 cm was excised from a 28-year-man who had presented with pain and swelling of the right shoulder for 5 years. Histopathologically, the tumor was composed of cells with clear eosinophilic cytoplasm and an epithelioid appearance in a myxoid str...
متن کاملParachordoma/myoepithelioma of the kidney: first report of a myxoid mimicry in an unusual location.
We report a case of parachordoma (or myoepithelioma) of the right upper kidney in a 56 year-old male patient. Light microscopic features of the tumor exhibited epithelioid, glomoid, and spindle cells with eosinophilic and vacuolated cytoplasm as well as round to oval nuclei. These cells were embedded in a myxoid and hyaline stroma separated by a fibrous tissue with minimal cellular atypia and a...
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ژورنال
عنوان ژورنال: Gazi Medical Journal
سال: 2014
ISSN: 2147-2092
DOI: 10.12996/gmj.2014.21