[胃肠道多发性淋巴瘤性息肉病：1例突尼斯病例]
[Multiple lymphomatous polyposis of the gastrointestinal tract: a Tunisian case].
作者信息
Karoui Sami, Kchir Nidhameddine, Jemni Fatma, Khalfallah Samir, Boubaker Jalel, Boussen Haomouda, Zitouna Mohamed Moncef, Filali Azza
机构信息
Service de Gastro-entérologie A, Hôpital la Rabta, Tunis.
出版信息
Tunis Med. 2004 May;82(5):457-60.
Multiple lymphomatous polyposis is a distinctive primary gastrointestinal lymphoma which endoscopical, histopathological et immunophenotypical characteristics are well known. This lymphoma is rare and its prognosis is bad because of frequency of stage IV patients. We report the case of a 75-year-old male patient with multiple lymphomatous polyposis affecting the rectum, the colon and the stomach associated with an involvement of lymphadenopathies, bone marrow and liver. Treatment by chemotherapy was ineffective and patient dead after 3 sessions of CEOP protocol.
多发性淋巴瘤性息肉病是一种独特的原发性胃肠道淋巴瘤，其内镜、组织病理学及免疫表型特征已为人熟知。这种淋巴瘤较为罕见，由于IV期患者比例较高，其预后较差。我们报告一例75岁男性患者，患有累及直肠、结肠和胃的多发性淋巴瘤性息肉病，并伴有淋巴结、骨髓和肝脏受累。化疗无效，患者在接受3个疗程的CEOP方案治疗后死亡。
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