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作 者:Roetman B. Schildhauer T. A. Kuhnen C. 王铮(译) 陈云茹(校)
机构地区:[1]BG-Kliniken Bergmannsheil, Universitatsklinik Chirurigische Klinik und Poliklinik, Burkle-de-laCamp Platz 1, DE-44789 Bochum, Germany [2]不详
出 处:《世界核心医学期刊文摘(胃肠病学分册)》2006年第6期52-53,共2页Core Journals in Gastroenterology
摘 要:In contrast to common colonic epithelial neoplasms, polypoid mesenchymal tumors of the colon are extremely rare. The majority of uncommon gastrointestinal mesenchymal tumors are associated with the so-called gastrointestinal stromal tumors (GIST). We present a case of a rare colonic pleomorphic sarcoma, macroscopically mimicking a common epithelial colonic polyp, which did not match the criteria of GIST. In this case report we discuss the clinical and pathological characteristics of a rare polypoid-shaped, pleomorphic colonic sarcoma and refer a mark-off to other rare mesenchymal neoplasms of the gut.In contrast to common colonic epithelial neoplasms, polypoid mesenchymal tumors of the colon are extremely rare. The majority of uncommon gastrointestinal mesenchymal tumors are associated with the so-called gastrointestinal stromal tumors (GIST). We present a case of a rare colonic pleomorphic sarcoma, macroscopically mimicking a common epithelial colonic polyp, which did not match the criteria of GIST. In this case report we discuss the clinical and pathological characteristics of a rare polypoid-shaped, pleomorphic colonic sarcoma and refer a mark-off to other rare mesenchymal neoplasms of the gut.
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