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胃肠道神经节瘤。与冯·雷克林豪森病及其他多肿瘤综合征的关系。

Ganglioneuromas of the gastrointestinal tract. Relation to Von Recklinghausen disease and other multiple tumor syndromes.

作者信息

Shekitka K M, Sobin L H

机构信息

Division of Gastrointestinal Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000.

出版信息

Am J Surg Pathol. 1994 Mar;18(3):250-7.

PMID:7906923
Abstract

We studied 43 patients with ganglioneuromas of the gastrointestinal tract accessioned at the Armed Forces Institute of Pathology (AFIP) from 1940 to 1990 in order to determine their relation to von Recklinghausen's disease and other multiple tumor syndromes. They fell into three groups: polypoid ganglioneuroma (28 patients); ganglioneuromatous polyposis (7 patients); and diffuse ganglioneuromatosis (8 patients). Follow-up (1-24 years, average 8 years) for 16 of 28 patients with polypoid ganglioneuroma showed that none of these patients developed von Recklinghausen's disease or evidence or multiple tumor syndromes. Three of seven patients with ganglioneuromatous polyposis were alive and well but were reported to have multiple cutaneous lipomas and one reported a family history of multiple intestinal polyps. For seven of eight patients, diffuse ganglioneuromatosis was associated with other tumors, namely multiple endocrine neoplasia type IIb, multiple ganglioneuromas and neurofibromas limited to the gastrointestinal tract, von Recklinghausen's disease and neurogenic sarcoma. We conclude that the solitary polypoid ganglioneuroma of the gastrointestinal tract is not associated with the subsequent development of von Recklinghausen's disease or multiple endocrine neoplasia. All three forms of gastrointestinal ganglioneuromatous disease appear to be largely centered in the colon and rectum, unlike neurofibromas and neurofibromatosis, which, in our experience, occur more commonly in the small intestine and stomach.

摘要

我们研究了1940年至1990年期间在美国武装部队病理研究所(AFIP)登记的43例胃肠道神经节瘤患者,以确定它们与冯·雷克林豪森病及其他多发肿瘤综合征的关系。患者分为三组:息肉样神经节瘤(28例);神经节瘤性息肉病(7例);弥漫性神经节瘤病(8例)。对28例息肉样神经节瘤患者中的16例进行了随访(1 - 24年,平均8年),结果显示这些患者均未发生冯·雷克林豪森病或出现多发肿瘤综合征的证据。7例神经节瘤性息肉病患者中有3例存活且状况良好,但据报告患有多发性皮肤脂肪瘤,1例有家族性多发性肠息肉病史。8例弥漫性神经节瘤病患者中有7例与其他肿瘤相关,即IIb型多发性内分泌肿瘤、局限于胃肠道的多发性神经节瘤和神经纤维瘤、冯·雷克林豪森病及神经源性肉瘤。我们得出结论,胃肠道孤立性息肉样神经节瘤与冯·雷克林豪森病或多发性内分泌肿瘤的后续发生无关。胃肠道神经节瘤病的所有三种形式似乎主要集中在结肠和直肠,这与神经纤维瘤和神经纤维瘤病不同,据我们的经验,神经纤维瘤和神经纤维瘤病更常见于小肠和胃。

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