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盆腔脂肪增多症——一种罕见的诊断及具有挑战性的治疗:一例病例报告及文献综述

Pelvic lipomatosis-a rare diagnosis and a challenging management: a case report and literature review.

作者信息

Ata Yaser M, Al-Jassim Fatima A, Alabassi Kholoud, Albakr Ahmed, Ismail Taha, Al Jalham Khalid

机构信息

Urology Department, Hamad Medical Corporation, Doha, Qatar.

出版信息

J Surg Case Rep. 2024 Dec 15;2024(12):rjae777. doi: 10.1093/jscr/rjae777. eCollection 2024 Dec.

Abstract

Pelvic lipomatosis (PL) involves nonmalignant excess fat growth in perirectal and perivesical areas, gaining recognition over three decades. This review addresses its clinicopathological aspects amid controversies, emphasizing the need for a comprehensive examination of current literature. This report outlines a 42-year-old man's diagnostic journey for persistent urological symptoms, ultimately identified as PL. PL, if untreated, adversely impacts the urinary system, affecting kidney function and causing systemic complications. Management involves accurate diagnosis through radiological methods and surgical intervention, aiming to alleviate symptoms and enhance affected individuals' quality of life.

摘要

盆腔脂肪增多症(PL)是指直肠周围和膀胱周围区域出现非恶性的脂肪过度生长,三十多年来一直受到关注。本综述在争议中探讨其临床病理方面,强调需要对当前文献进行全面审视。本报告概述了一名42岁男性因持续泌尿系统症状的诊断过程,最终确诊为PL。PL若不治疗,会对泌尿系统产生不利影响,影响肾功能并引发全身并发症。治疗包括通过放射学方法进行准确诊断以及手术干预,旨在缓解症状并提高患者的生活质量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1eec/11646686/8859d3eaec8f/rjae777f1.jpg

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