| Literature DB >> 27134707 |
Despoina Mourtzoukou1, Shane Zaidi1, Robin L Jones1, Cyril Fisher1, Khin Thway1.
Abstract
Myoepithelial neoplasms of the soft tissues are a rare, heterogeneous group of tumors for which classification continues to evolve. While well defined within salivary glands, they can also arise in viscera and soft tissues, where diagnosis is challenging due to the lack of clinical and pathological familiarity. We present the case of a 36 year old man with myoepithelial carcinoma arising as a primary tumor within the soft tissues of the neck, which metastasized to the cecum, causing intussusception. This spindle cell neoplasm showed the classic S100 protein, smooth muscle actin and pancytokeratin-positive immunoprofile. Metastasis of myoepithelial carcinoma to the cecum has not been previously described, and coupled with the spindle cell morphology, may cause significant diagnostic difficulty in the absence of clinical familiarity, particularly as there is morphologic overlap with spindle cell neoplasms arising more commonly in gastrointestinal sites, including gastrointestinal stromal tumor, leiomyosarcoma and sarcomatoid carcinoma.Entities:
Keywords: EWSR1; INI1 loss; Myoepithelial carcinoma; bowel; cecum; fusion transcripts; intussusception; metastasis; soft tissue
Year: 2016 PMID: 27134707 PMCID: PMC4827644 DOI: 10.4081/rt.2016.6086
Source DB: PubMed Journal: Rare Tumors ISSN: 2036-3605