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产生甲胎蛋白的直肠癌——病例报告

alpha-Fetoprotein-producing rectal carcinoma--a case report.

作者信息

Taguchi J, Yano H, Sueda J, Yamaguchi R, Kojiro M, Shirouzu G, Hashimoto K

机构信息

Department of Pathology, Kurume University School of Medicine, Japan.

出版信息

Kurume Med J. 1997;44(4):339-48. doi: 10.2739/kurumemedj.44.339.

Abstract

A case with an alpha-fetoprotein (AFP)-producing carcinoma originating from the rectum is described. A 71-year-old male patient, who underwent a rectectomy for rectal carcinoma, developed space occupying lesions in the liver and a remarkable AFP elevation (220,000 ng/ml) in the 6th month postoperatively, and then expired one year later. Histologically, the rectal carcinoma consisted of well-differentiated adenocarcinomas, and contiguous cancerous cells proliferating in either a medullary or trabecular pattern. In the "trabecular" areas, localization of AFP was confirmed immunohistochemically. Results of concanavalin A or lens culinaris agglutinin affinity chromatography demonstrated that it was between a hepatic type and a yolk sac type, and was considered to be an intestinal type. This could have been an AFP-producing rectal carcinoma, in which the patient experienced liver metastasis at a relatively early postoperative period and died. This shows that AFP-producing rectal carcinomas are highly malignant, biologically, similar to AFP-producing gastric cancers.

摘要

本文描述了一例源自直肠的产生甲胎蛋白(AFP)的癌。一名71岁男性患者因直肠癌接受了直肠切除术,术后6个月肝脏出现占位性病变,AFP显著升高(220,000 ng/ml),一年后死亡。组织学上,直肠癌由高分化腺癌组成,连续的癌细胞呈髓样或小梁状增殖。在“小梁”区域,免疫组织化学证实了AFP的定位。伴刀豆球蛋白A或扁豆凝集素亲和层析结果表明,它介于肝型和卵黄囊型之间,被认为是肠型。这可能是一例产生AFP的直肠癌,患者在术后相对早期发生肝转移并死亡。这表明,产生AFP的直肠癌具有高度恶性,在生物学上与产生AFP的胃癌相似。

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