Smir B N, Pulitzer D R
Department of Pathology, University of Texas Health Science Center, San Antonio 78284-7750.
J Clin Gastroenterol. 1994 Sep;19(2):139-42. doi: 10.1097/00004836-199409000-00014.
Multiple lymphomatous polyposis (MLP) is a term used to describe malignant lymphomas of the gastrointestinal tract that manifest as polyposis. The cell population of MLP is identical to that in "mantle cell lymphoma." In most instances, relatively small segments of small and large intestine are affected. We report a case of MLP in which involvement was unusually widespread. A 56-year-old man, with abdominal pain and weight loss, proved to have a large mass at the ileocecal valve as well as multiple polyps of the stomach and small and large intestine. MLP is distinctive both grossly and microscopically. Clinically, it may be confused with epithelial polyps, and histologically it must be distinguished from benign lymphoid proliferations as well as other types of lymphoma. The latter distinction is important because of the relatively poor prognosis (median survival of < 3 years).
多发性淋巴瘤性息肉病(MLP)是一个用于描述表现为息肉病的胃肠道恶性淋巴瘤的术语。MLP的细胞群体与“套细胞淋巴瘤”中的细胞群体相同。在大多数情况下,小肠和大肠相对较小的节段会受到影响。我们报告一例MLP,其受累情况异常广泛。一名56岁男性,有腹痛和体重减轻症状,经证实回盲瓣处有一个大肿块,胃以及小肠和大肠有多个息肉。MLP在大体和显微镜下都有其独特之处。临床上,它可能与上皮性息肉相混淆,组织学上必须与良性淋巴样增生以及其他类型的淋巴瘤相鉴别。后一种鉴别很重要,因为其预后相对较差(中位生存期<3年)。