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一名成年女性腹膜罕见钙化性纤维性假瘤,为腹腔镜手术中的偶然发现。

Rare calcifying fibrous pseudotumor of the peritoneum in an adult woman as a random finding during laparoscopic surgery.

作者信息

Topis Spyridon, Samaras Menelaos, Potiris Anastasios, Machairiotis Nikolaos, Drakakis Peter, Stavros Sofoklis

机构信息

Third Department of Obstetrics and Gynecology University General Hospital "ATTIKON", Medical School, National and Kapodistrian University of Athens Athens Greece.

Second Department of Pathology, University General Hospital "ATTIKON" Medical School, National and Kapodistrian University of Athens Athens Greece.

出版信息

Clin Case Rep. 2024 Aug 29;12(9):e9384. doi: 10.1002/ccr3.9384. eCollection 2024 Sep.

DOI:10.1002/ccr3.9384
PMID:39219773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11362017/
Abstract

Calcifying fibrous pseudotumors (CFT) are rare benign lesions diagnosed by histological and immunohistochemical studies. Our case presents a rare detection of a CFT in the parietal peritoneum. These lesions can be falsely interpreted as myomas or adnexal masses and thus gynecologists should be aware of the existence of CFTs.

摘要

钙化性纤维性假瘤(CFT)是通过组织学和免疫组织化学研究诊断出的罕见良性病变。我们的病例显示在腹膜顶发现了罕见的CFT。这些病变可能被误诊为肌瘤或附件肿块,因此妇科医生应了解CFT的存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b008/11362017/5a5150851072/CCR3-12-e9384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b008/11362017/4683ba8d9cb3/CCR3-12-e9384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b008/11362017/5a5150851072/CCR3-12-e9384-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b008/11362017/4683ba8d9cb3/CCR3-12-e9384-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b008/11362017/5a5150851072/CCR3-12-e9384-g002.jpg

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本文引用的文献

1
Calcifying Fibrous Tumor: Review of 157 Patients Reported in International Literature.钙化性纤维性肿瘤:国际文献报道的157例患者回顾
Medicine (Baltimore). 2016 May;95(20):e3690. doi: 10.1097/MD.0000000000003690.
2
Calcifying fibrous pseudotumour: a case report.钙化性纤维性假瘤:一例报告
Indian J Pathol Microbiol. 2007 Oct;50(4):831-2.
3
Childhood fibrous tumor with psammoma bodies. Clinicopathologic features in two cases.伴有砂粒体的儿童纤维瘤。两例临床病理特征
Arch Pathol Lab Med. 1988 Aug;112(8):798-800.