Inflammatory Myofibroblastic Tumor of the Sigmoid Colon in an Infant: A Case Report and Literature Review

被引：4

作者：

Wu, Luyao ^{[1
]}

Meng, Xinyao ^{[1
]}

Wang, Jing ^{[1
]}

Wang, Qiong ^{[1
]}

Sun, Xiaoyi ^{[1
]}

Zhu, Tianqi ^{[1
]}

Yu, Donghai ^{[1
]}

Feng, Jiexiong ^{[1
]}

机构：

[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, Dept Pediat Surg, Wuhan 430030, Peoples R China

来源：

FETAL AND PEDIATRIC PATHOLOGY | 2023年 / 42卷 / 01期

基金：

中国国家自然科学基金;

关键词：

Case report; diagnosis; inflammatory myofibroblastic tumor; pathology; sigmoid colon; PSEUDOTUMOR; SARCOMA; LIVER;

D O I：

10.1080/15513815.2022.2062500

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

Background: Inflammatory myofibroblastic tumor (IMT) infrequently involves the sigmoid colon, and has not previously been described in an infant sigmoid colon. Case report: An inflammatory myofibroblastic tumor arose from the sigmoid colon of an 11-month-old boy, confirmed by anaplastic lymphoma kinase (ALK), smooth muscle actin (SMA) and desmin immunohistochemical staining. The patient recovered well after complete resection of the tumor. Discussion: Sigmoid IMT can occur in infancy. This eighth case is the youngest so far. The child did well after surgical resection.

引用

页码：123 / 130

页数：8

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