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[肠道恶性组织细胞增多症。一例解剖临床病例报告]

[Malignant histiocytosis of the intestine. An anatomo-clinical case report].

作者信息

Nézelof C, Duhamel J F, Arnaud-Battandier F, Bresson J L, Borel B, Bigel P, Ricour C

出版信息

Arch Fr Pediatr. 1983 Dec;40(10):775-80.

PMID:6608934
Abstract

Clinico-pathological case report of a 11 year-old girl who successively presented persistent abdominal pain, pneumoperitoneum, repeated intestinal hemorrhages, superficial intestinal ulcerations, first localized on the jejunum and later extended to the all gut. After a course of 13 months, the child died from diffuse and repeated hemorrhages. The morphologic studies revealed a diffuse and homogeneous cellular infiltrate made of large round "lymphomatous" cells scattered within the lamina propria and submucosa. Initially this superficial cellular infiltrate was overshadowed by accompanying inflammatory cells and was not recognized as a tumoral process. Later on the dissemination of abnormal cells to the entire ileon, mesenteric lymph nodes, spleen and liver and the cellular appearance confirmed its neoplastic nature and allowed to consider this process as a malignant histiocytosis of the intestine as described by Isaacson and Wright. This case seems to be the first case reported in childhood.

摘要

一名11岁女孩的临床病理病例报告,该女孩先后出现持续性腹痛、气腹、反复肠道出血、浅表性肠道溃疡,最初局限于空肠,后来扩展至整个肠道。经过13个月的病程,该患儿死于弥漫性反复出血。形态学研究显示,在固有层和黏膜下层有由大的圆形“淋巴瘤样”细胞组成的弥漫性均匀细胞浸润。最初,这种浅表性细胞浸润被伴随的炎症细胞掩盖,未被识别为肿瘤性病变。后来,异常细胞扩散至整个回肠、肠系膜淋巴结、脾脏和肝脏,细胞表现证实了其肿瘤性质,可将此过程视为Isaacson和Wright所描述的肠道恶性组织细胞增生症。该病例似乎是儿童期报告的首例。

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