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先天性婴儿乙状结肠纤维肉瘤 1 例,新生儿表现为气腹。

A case of congenital infantile fibrosarcoma of sigmoid colon manifesting as pneumoperitoneum in a newborn.

机构信息

Division of Pediatric Surgery, Department of Surgery, Pusan National University School of Medicine, Yangsan, Korea.

出版信息

J Korean Med Sci. 2013 Jan;28(1):160-3. doi: 10.3346/jkms.2013.28.1.160. Epub 2013 Jan 8.

Abstract

Congenital infantile fibrosarcoma (CIF) is a rare soft-tissue tumor in the pediatric age group and seldom involves the gastrointestinal tract. A 2-day-old boy was transferred to our hospital with a pneumpoperitoneum. After emergency operation, we could find a solid mass wrapping around a sigmoid colon and performed a segmental resection of sigmoid colon including a mass. Histopathologic examination showed an infantile fibrosarcoma origining from the muscular layer of colon. The baby was discharged on the 17th hospital day and followed for 1 yr without recurrence.

摘要

先天性婴儿纤维肉瘤(CIF)是一种罕见的儿科软组织肿瘤,很少累及胃肠道。一名 2 天大的男婴因气腹转入我院。急诊手术后,我们发现一个包裹在乙状结肠周围的实性肿块,并进行了包括肿块的乙状结肠节段切除术。组织病理学检查显示起源于结肠肌肉层的婴儿纤维肉瘤。患儿于第 17 天出院,随访 1 年无复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4be6/3546097/d2521f3084f3/jkms-28-160-g001.jpg

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