| Literature DB >> 29458068 |
Ying Zhang1, Lin Tao1, Can Yin1, Weiwei Wang2, Hong Zou1, Yan Ren1, Weihua Liang1, Jinfang Jiang1, Wenjie Zhang1, Wei Jia3, Feng Li4.
Abstract
Ovarian microcystic stromal tumor is a relatively rare tumor type. This tumor is characterized by a unique microcyst structure, and essentially all tumors show benign biological behavior. Here, we report a case with a primary ovarian microcystic stromal tumor that experienced recurrence. Pathological findings showed that the original tumor, relapsed tumor in the ovary, and the recurrent tumor in the iliac fossa presented similar histologic features. The tumor mainly consisted of microcysts, solid cellular regions, and a fibrous stroma. Immunohistochemically, the tumor cells were positive for β-catenin, CD10, vimentin, and WT-1. Mutational analysis revealed a missense mutation (c.1590C>T; pG530E) in exon 15 of the APC gene and another missense mutation (c.740G>A; pA247V) in exon 1 of the KRAS gene. We also reviewed other published cases to evaluate the prognosis and treatment. This is the first report to describe a microcystic stromal tumor of the ovary presenting with undetermined biological potential.Entities:
Keywords: APC gene; Immunohistochemistry; Microcystic stromal tumor of the ovary; Mutation; β-Catenin gene
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Year: 2018 PMID: 29458068 DOI: 10.1016/j.humpath.2018.02.012
Source DB: PubMed Journal: Hum Pathol ISSN: 0046-8177 Impact factor: 3.466