Desmoid-type fibromatosis difficult to distinguish from GIST : A case report

被引:0
|
作者
Takehara, Yukako [1 ]
Yoshikawa, Kozo [1 ]
Tokunaga, Takuya [1 ]
Nishi, Masaaki [1 ]
Takasu, Chie [1 ]
Kashihara, Hideya [1 ]
Yoshimoto, Toshiaki [1 ]
Shimada, Mitsuo [1 ]
机构
[1] Univ Tokushima, Tokushima Univ, Dept Surg, Tokushima, Japan
来源
JOURNAL OF MEDICAL INVESTIGATION | 2020年 / 67卷 / 3-4期
关键词
Desmoid-type fibromatosis; Diagnosis; Surgery;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background : Desmoid-type fibromatosis is a very rare disease that has no characteristic image findings, so it is often difficult to differentiate from gastrointestinal stromal tumor (GIST). A case of desmoid-type fibromatosis that was difficult to differentiate from GIST is reported. The decisive factor in the diagnosis was positive nuclear immunostaining for beta-catenin nucleus. Case presentation : A man is his 30s had no significant past medical history, including no abdominal surgery. A medical check-up found a large tumor in the right lateral abdomen. After some examinations, a preoperative diagnosis of GIST was made, and open ileocecal resection was performed. However, the final diagnosis based on the pathological findings was desmoid-type fibromatosis. Conclusions : We should consider desmoid-type fibromatosis when we find a large abdominal mass, but it may be difficult to diagnose based only on imaging findings. Immunohistochemical examination of the specimen may make the diagnosis. J. Med. Invest. 67 : 375-377, August, 2020
引用
收藏
页码:375 / 377
页数:3
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