Pross M, Manger T, Schulz H U, Lippert H, Roessner A, Günther T
Klinik und Poliklinik für Chirurgie, Otto-von-Guericke Universität Magdeburg.
Chirurg. 1999 Jul;70(7):807-12. doi: 10.1007/s001040050728.
Gastrointestinal stromal tumors (GIST), which form a rare group of neoplasias of the gastrointestinal tract, have not yet been fully investigated. Although good progress has been made in their diagnosis, classification of these lesions with regard to their histogenesis and biological behavior remains problematic. Between 1994 and 1998, 18 GIST patients underwere operation in the Department of Surgery. Twelve of these patients (67%) had stromal tumors in the stomach, and six (33%) had intestinal stromal tumors. The primary tumor could be removed in all patients with R0 resection. Six patients developed hematogenous liver metastasis, with the size of their primary tumor exceeding 10 cm. Extrahepatic distant metastases were not found in any case. Lymphadenectomy showed that lymph node metastases did not occur. Histological evaluation was made according to the guidelines of Lewin, Weinstein and Riddell. Currently established therapy is limited to complete surgical resection of the primary tumor and its metastases. Adjuvant or neoadjuvant chemotherapy approaches have failed.
胃肠道间质瘤(GIST)是一组罕见的胃肠道肿瘤,目前尚未得到充分研究。尽管在其诊断方面取得了良好进展,但这些病变在组织发生和生物学行为方面的分类仍然存在问题。1994年至1998年间,18例GIST患者在外科接受了手术。其中12例患者(67%)胃部有间质瘤,6例(33%)有肠道间质瘤。所有患者均通过R0切除成功切除了原发肿瘤。6例患者发生了血行性肝转移,其原发肿瘤大小超过10厘米。未发现任何肝外远处转移病例。淋巴结清扫显示未发生淋巴结转移。组织学评估按照Lewin、Weinstein和Riddell的指南进行。目前既定的治疗方法仅限于对原发肿瘤及其转移灶进行完整的手术切除。辅助或新辅助化疗方法均告失败。