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双侧后天性肾周淋巴管扩张症:病例报告

Bilateral acquired Perirenal Lymphangiectasia: case report.

作者信息

Peñaherrera-Vásquez Daniel, Peñaherrera Diego, Fuenmayor-González Luis

机构信息

Facultad de Ciencias Médicas, Universidad Central del Ecuador, Iquique and Sodiro St - Quito 170403, Ecuador.

UROMEDIK Urology Center, Belisario Quevedo Ave and Marqués de Maenza St - Latacunga 050101, Ecuador.

出版信息

Oxf Med Case Reports. 2025 Jun 27;2025(6):omaf086. doi: 10.1093/omcr/omaf086. eCollection 2025 Jun.

DOI:10.1093/omcr/omaf086
PMID:40585461
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12202297/
Abstract

Bilateral perirenal lymphangiectasia is a rare condition characterized by the dilation of lymphatic ducts and the formation of fluid-filled cavities. Renal lymphangiectasia is rarely observed, affecting approximately 1% of cases, with only 34 bilateral cases reported in adults by 2025. This case report discusses a 55-year-old male with a history of recurrent pyelonephritis who was eventually diagnosed with bilateral acquired perirenal lymphangiectasia based on CT, MRI, and cytochemical analysis of perirenal fluid. The patient exhibited mild left flank pain without further complications, and given the disease's benign nature, an expectant management approach was adopted. Follow-up assessments confirmed an asymptomatic status. This report highlights the importance of considering lymphangiectasia in differential diagnoses for renal cystic lesions to avoid unnecessary procedures. Our case is the 35th documented instance of bilateral renal lymphangiectasia in the literature, underscoring the need for medical awareness of this condition to improve diagnosis and patient care.

摘要

双侧肾周淋巴管扩张症是一种罕见疾病,其特征为淋巴管扩张以及形成充满液体的腔隙。肾淋巴管扩张症很少见,约占病例的1%,截至2025年,成人双侧病例仅报告了34例。本病例报告讨论了一名55岁男性,有复发性肾盂肾炎病史,最终根据CT、MRI以及肾周液体的细胞化学分析诊断为双侧后天性肾周淋巴管扩张症。患者表现为轻度左侧腰痛,无进一步并发症,鉴于该疾病的良性性质,采取了观察等待的管理方法。随访评估证实患者无症状。本报告强调了在肾囊性病变的鉴别诊断中考虑淋巴管扩张症以避免不必要手术的重要性。我们的病例是文献中记录的第35例双侧肾淋巴管扩张症,强调了提高对该疾病的医学认识以改善诊断和患者护理的必要性。

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本文引用的文献

1
Bilateral renal lymphangiectasia: Literature review of a rare entity.双侧肾淋巴管扩张症:一种罕见疾病的文献回顾。
Saudi Med J. 2024 May;45(5):537-540. doi: 10.15537/smj.2024.45.5.20231019.
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Renal lymphangiectasia in pediatric population: case series and review of literature.小儿肾淋巴管扩张症:病例系列及文献复习。
Ann Saudi Med. 2022 Mar-Apr;42(2):139-144. doi: 10.5144/0256-4947.2022.139. Epub 2022 Apr 7.
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Bilateral Renal Lymphangiectasia with No Significant Morbidity for Over 25 Years: A Case Report.双侧肾淋巴管扩张症 25 年以上无明显发病:一例报告。
Am J Case Rep. 2021 Nov 8;22:e933934. doi: 10.12659/AJCR.933934.
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Renal Lymphangiectasia: An Unusual Mimicker of Cystic Renal Disease - A Case Series and Literature Review.肾淋巴管扩张症:一种罕见的囊性肾病模仿者——病例系列及文献综述
Cureus. 2020 Oct 8;12(10):e10849. doi: 10.7759/cureus.10849.
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Gorham disease: lymphangiomatosis with massive osteolysis.戈勒姆病:伴有大量骨质溶解的淋巴管瘤病。
Clin Imaging. 2017 Jan-Feb;41:83-85. doi: 10.1016/j.clinimag.2016.10.007. Epub 2016 Oct 18.
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Bilateral Renal Lymphangiectasia.双侧肾淋巴管扩张症
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J Clin Imaging Sci. 2015 Jan 30;5:6. doi: 10.4103/2156-7514.150449. eCollection 2015.
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Bilateral renal lymphangiomatosis: imaging and histopathologic findings.双侧肾淋巴管瘤病:影像学和组织病理学表现
Abdom Imaging. 2013 Aug;38(4):858-62. doi: 10.1007/s00261-012-9977-0.
9
Renal lymphangiectasia presented by pleural effusion and ascites.肾淋巴管扩张症表现为胸腔积液和腹水。
J Radiol Case Rep. 2009;3(10):5-10. doi: 10.3941/jrcr.v3i10.317. Epub 2009 Oct 1.
10
Perirenal fluid collections and monoclonal gammopathy.肾周液体积聚和单克隆丙种球蛋白血症。
Nephrol Dial Transplant. 2012 Jan;27(1):448-9. doi: 10.1093/ndt/gfr433. Epub 2011 Aug 2.