Primary Ovarian Solid Pseudopapillary Neoplasm With CTNNB1 c.98C>G (p.S33C) Point Mutation

被引:14
作者
Singh, Kamaljeet [1 ]
Patel, Nimesh [2 ]
Patil, Pallavi [2 ]
Paquette, Cherie [1 ]
Mathews, Cara A. [3 ]
Lawrence, W. Dwayne [1 ]
机构
[1] Brown Univ, Women & Infants Hosp Rhode Isl, Alpert Med Sch, Dept Pathol & Lab Med, Providence, RI 02912 USA
[2] Brown Univ, Rhode Isl Hosp, Alpert Med Sch, Dept Pathol & Lab Med, Providence, RI 02903 USA
[3] Women & Infants Hosp Rhode Isl, Program Womens Oncol, Providence, RI USA
基金
美国国家卫生研究院; 英国惠康基金;
关键词
Ovary; Solid papillary neoplasm; Catenin; Point mutation; Extrapancreatic; OF-THE-LITERATURE; MICROCYSTIC STROMAL TUMOR; BETA-CATENIN MUTATION; E-CADHERIN; GENE-EXPRESSION; CYSTIC TUMOR; PANCREAS; ORIGIN; MESOCOLON; PATHWAYS;
D O I
10.1097/PGP.0000000000000396
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Ovary is one of the extrapancreatic sites of origin of solid pseudopapillary neoplasm (SPN). Only 9 cases of primary ovarian SPN, 1 with CTNNB1 mutation similar to pancreatic SPN, have been reported in the English literature. We describe the second case of ovarian SPN with confirmed CTNNB1 mutation. A 49-year-old postmenopausal woman presented with a 4.5 cm right ovarian mass. Ovarian mass showed histologic and immunohistochemical features of pancreatic SPN. The ovarian surface was intact and uninvolved. Ki-67 index was low (1%-5%). DNA sequencing of CTNNB1 exon 3 revealed c.98C>G (p.S33C), a well-characterized activating mutation. Our case adds to the growing body of evidence that primary ovarian SPN are phenotypically and genotypically similar to pancreatic SPN.
引用
收藏
页码:110 / 116
页数:7
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