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作 者:Constantine I.Fotiadis Ilias A.Kouerinis Ioannis Papandreou George C.Zografos George Agapitos
机构地区:[1]Third Department of Propaudeutic SurgeryUniversity of Athens,Sotiria Hospital,Athens, Greece [2]First Department of Propaudeutic SurgeryUniversity of Athens,Hippokration Hospital,Athens,Greece [3]Third Department of Propaudeutic SurgeryUniversity of Athens,Sotiria Hospital,Athens,Greece
出 处:《World Journal of Gastroenterology》2005年第32期5079-5081,共3页世界胃肠病学杂志(英文版)
摘 要:Schwannomas are rare tumors derived from the cells of Schwann that form the neural sheath. When located in the gastrointestinal tract, they constitute together with leiomyoma, leiomyoblastoma, and leiomyosarcoma, the gastrointestinal stromal tumors (GIST). Peripheral nerve sheath tumors represent 2-6% GIST with most common location, the stomach and the small intestine. Schwannomas of the colon and rectum are extremely rare and radical excision with wide margins is mandatory, due to their tendency to recur locally and become malignant, if left untreated. In the present study, we report a rare case of a sigmoid schwannoma, which was successfully treated in our department and reviewed the literature.Schwannomas are rare tumors derived from the cells of Schwann that form the neural sheath. When located in the gastrointestinal tract, they constitute together with leiomyoma, leiomyoblastoma, and leiomyosarcoma, the gastrointestinal stromal tumors (GIST). Peripheral nerve sheath tumors represent 2-6% GIST with most common location, the stomach and the small intestine. Schwannomas of the colon and rectum are extremely rare and radical excision with wide margins is mandatory, due to their tendency to recur locally and become malignant, if left untreated. In the present study, we report a rare case of a sigmoid schwannoma, which was successfully treated in our department and reviewed the literature.
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