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Fertility-sparing operation for recurrence of uterine cervical perivascular epithelioid cell tumor
Author(s) -
Eiko Yamamoto,
Kazuhiko Ino,
Maiko Sakurai,
Sachiko Takigawa,
Akira Iwase,
Fumitaka Kikkawa
Publication year - 2010
Publication title -
rare tumors
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.285
H-Index - 15
eISSN - 2036-3613
pISSN - 2036-3605
DOI - 10.4081/rt.2010.e26
Subject(s) - medicine , perivascular epithelioid cell , uterus , malignancy , cervix , hysterectomy , epithelioid cell , uterine cervix , pathology , carcinoma , cancer , immunohistochemistry
Perivascular epithelioid cell tumors (PEComa) are mesenchymal tumors composed of histologically and immunohistochemically distinctive perivascular epithelial cells. Although the uterine corpus seems to be one of the most prevalent sites of involvement, PEComa of the uterine cervix are very rare. Only four cervical PEComa cases have been described, and were treated with hysterectomy and radiotherapy. We report a case of a 24-year-old nulligravida woman who presented with acute abdominal pain and was diagnosed with a rupture of an ovarian chocolate cyst. Subsequent surgery revealed that the tumor arose in the uterus, and the histological diagnosis was uterine PEComa with low potential malignancy. Recurrent PEComa in the uterine cervix were excised twice, and she remains disease free 12 months after the last operation. To the best of our knowledge, this is the first report of recurrent cervical PEComa with fertility-preserving surgery. Estimating the malignant potential and appropriate surgery are essential for young patients with uterine PEComa

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