نتایج جستجو برای: perivascular epithelioid cell neoplasms
تعداد نتایج: 1960755 فیلتر نتایج به سال:
UNLABELLED Perivascular epithelioid cell tumors (PEComas) encompass a group of rare mesenchymal neoplasms, which typically have a perivascular location with dual melanocytic and muscular differentiation. They are found in a variety of localizations, though lesions in the liver are exceedingly rare. Because of their rarity, the clinical, radiological and histological features of these tumors hav...
Primary perivascular epithelioid cell tumor neoplasm (PEComa) of bone is extremely rare. To our knowledge, only 11 cases of PEComa primarily arising in bone have been described. Herein, we present one case of primary bone PEComa which occurs in the thigh.
Abstract Perivascular epithelioid cell tumours of the uterus are rare neoplasms with only few cases described in literature. Ongoing contribution to literature is important order understand natural history for diagnosis and management challenges PEComa. We present two contrasting PEComa who presented postmenopausal bleeding, were diagnosed on endometrial biopsy had surgical treatment. The first...
BACKGROUND The World Health Organization recently recognized a family of neoplasms showing at least partial morphological or immunohistochemical evidence of a putative perivascular epithelioid cell (PEC) differentiation. These tumors include angiomyolipoma (AML), clear cell "sugar" tumors of the lung (CCST), lymphangioleiomyomatosis (LAM), clear cell myomelanocytic tumors of the falciform ligam...
Perivascular epithelioid cell tumor (PEComa) is an extremely rare neoplasm that appears to arise most commonly at visceral (especially gastrointestinal and uterine), retroperitoneal, and abdominopelvic sites. Malignant PEComas exist but are very rare. These tumors represent a family of mesenchymal neoplasms, mechanistically linked through activation of the mTOR signaling pathway. Metastatic PEC...
A patient presenting with a perivascular epithelioid cell tumor in the broad ligament: a case report
INTRODUCTION Perivascular epithelioid cell tumors are a family of rare mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelioid cells. They can originate in any visceral organ or soft tissue and include a range of lesions such as angiomyolipoma, clear cell 'sugar' tumor of the lung, lymphangioleiomyomatosis and clear cell myomelanocytic tumors...
Perivascular epithelioid cell tumors (PEComa) are tumors of perivascular epithelioid cells with immunohistochemical features of smooth muscle and melanocytic tumors. The PEComa of the gastrointestinal tract is rare. The treatment is surgical, although there are data that suggest a good response to rapamycin.
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