卵巢及阑尾同步黏液性癌:诊断缺陷1例及相关文献复习

IF 0.1 Q4 PATHOLOGY
Shaymaa E Hegazy, R. Bhargava, Somak Roy, E. Elishaev
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引用次数: 0

摘要

背景:原发性卵巢黏液性肿瘤的诊断有时会带来挑战,因为历史上大多数被诊断为原发性卵巢的肿瘤被记录为胃肠道和胰胆道的转移。这一挑战是由于卵巢原发性和转移性粘液瘤之间的重叠组织学特征,灰色地带。虽然原发性和转移性黏液性肿瘤的表现都表现为卵巢肿块的存在,但确定原发部位在临床上具有重要意义,因为大多数治疗指南都是基于原发组织。我们报告一个罕见的卵巢和阑尾粘液腺癌病例,其诊断缺陷和免疫组织化学特征的挑战。结论分子分析在卵巢肿瘤诊断中的应用有助于缩小灰色地带,减少原发性卵巢黏液性肿瘤的误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synchronous Mucinous Carcinomas of Ovary and Appendix: A Case Report With Diagnostic Pitfalls and Review of Corresponding Literature
Background Diagnosis of the primary ovarian mucinous neoplasms occasionally poses a challenge because historically most tumors diagnosed as primary ovarian were documented as metastases from gastrointestinal and pancreatobiliary tracts. This challenge is attributed to the overlapping histologic features, the gray zone, between primary and metastatic mucinous neoplasms in the ovary. While presentation of both primary and metastatic mucinous tumors manifests by the presence of an ovarian mass, determination of the site of origin is clinically significant, because most treatment guidelines are based on the tissue of origin. Case Presentation We present an unusual case of mucinous adenocarcinoma of the ovary and the appendix with diagnostic pitfalls and challenges of immunohistochemical profile. Conclusion Utilization of molecular analysis in challenging cases of ovarian neoplasms helps to narrow down the gray zone and lessens the misdiagnosis of primary ovarian mucinous tumors.
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