与多伊格-波特综合征相关的单发骨盆纤维性肿瘤:病例研究。

IF 0.9 Q4 ENDOCRINOLOGY & METABOLISM
Case Reports in Endocrinology Pub Date : 2024-10-14 eCollection Date: 2024-01-01 DOI:10.1155/2024/4584292
Wangjia Mao, Yuefang Sun, Shan Yan, Yuan Gao, Le Bu, Xiaoyun Cheng
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引用次数: 0

摘要

多吉-波特综合征(Doege-Potter syndrome,DPS)是一种非常罕见的副肿瘤性疾病,其特征是由单发纤维性肿瘤而非胰岛细胞肿瘤引起的低血糖。被称为单发纤维性肿瘤(SFTs)的软组织肿瘤非常罕见,这些肿瘤的起源部位各不相同,包括胸膜腔、纵隔、心包、腹膜后间隙、肝脏、甲状腺、眼眶、膀胱、肠道和软组织,而盆腔纤维性肿瘤则极为罕见。目前,国内外的病例记录和文献综述都极少。在本病例研究中,我们介绍了一名因恶性盆腔纤维性肿瘤而患上 DPS 的 82 岁女性。她的低血糖症在我院接受腹腔镜腹膜后肿瘤切除术后临床痊愈,此后生活质量得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Single Pelvic Fibrous Tumor Associated With Doege-Potter Syndrome: A Case Study.

Doege-Potter syndrome (DPS) is a very rare paraneoplastic condition that is marked by hypoglycemia brought on by a solitary fibrous tumor rather than an islet cell tumor. Soft tissue neoplasms termed as solitary fibrous tumors (SFTs) are rare and these tumors vary in the site of origin, from the pleural cavity, mediastinum, pericardium, retroperitoneal spaces, liver, thyroid, orbit, bladder, intestines, and soft tissues, while pelvic-derived fibrous tumors are incredibly unusual. There are currently extremely few documented cases and literature reviews both domestically and internationally. In this case study, we present an 82-year-old woman who developed DPS as a result of malignant pelvic SFTs. Her hypoglycemia was clinically healed after she underwent laparoscopic retroperitoneal tumor resection in our institution, and thereafter, her quality of life improved.

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来源期刊
Case Reports in Endocrinology
Case Reports in Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
2.10
自引率
0.00%
发文量
45
审稿时长
13 weeks
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