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化脓性汗腺炎并发阴茎阴囊淋巴水肿和肾淀粉样变性。

Hidradenitis supparativa complicated by penoscrotal lymphedema and renal amyloidosis.

机构信息

From the Department of Dermatology (Bin Rubaian, Al Zamami, Almuhaidib), College of Medicine, Imam Abdulrahman bin Faisal University, Dammam, and from the Department of Dermatology (Al Breiki), King Fahad Hospital of the University, Khobar, Kingdom of Saudi Arabia.

出版信息

Saudi Med J. 2022 Jul;43(7):751-754. doi: 10.15537/smj.2022.43.7.20220352.

DOI:10.15537/smj.2022.43.7.20220352
PMID:35830985
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9749683/
Abstract

Genital lymphedema usually develops after 4-30 years of chronic hidradenitis suppurativa (HS). However, our patient exhibited signs of it as early as 2 years after being diagnosed with HS. Renal amyloidosis is a rarely reported complication of HS. Unfortunately, our patient was asymptomatic but was found to have end-stage renal disease secondary to advanced renal amyloidosis. We report a case of a 42-year-old Indian gentleman who had HS for 9 years presenting with 2 rare complications: penoscrotal lymphedema and end-stage renal disease secondary to renal amyloidosis. The patient was treated with prednisolone and adalimumab to treat both his HS and renal amyloidosis, and was referred to general surgery to manage his genital lymphedema. We recommend following adult patients with moderate-to-severe HS and clinical duration of greater than 3 years and screening for amyloidosis before they reach end-stage organ disease, similar to what happened to our patient with end-stage renal disease.

摘要

生殖器淋巴水肿通常在慢性化脓性汗腺炎(HS)后 4-30 年内发展。然而,我们的患者在被诊断为 HS 后仅 2 年就出现了这种迹象。肾淀粉样变性是 HS 罕见的并发症。不幸的是,我们的患者无症状,但发现患有晚期肾淀粉样变性引起的终末期肾病。我们报告了一例 42 岁的印度男子,他患有 HS 9 年,出现了 2 种罕见的并发症:阴茎阴囊淋巴水肿和继发于肾淀粉样变性的终末期肾病。该患者接受了泼尼松龙和阿达木单抗治疗以治疗其 HS 和肾淀粉样变性,并被转介到普通外科手术以治疗其生殖器淋巴水肿。我们建议对患有中重度 HS 且临床病程大于 3 年的成年患者进行随访,并在达到终末期器官疾病之前筛查淀粉样变性,就像我们的终末期肾病患者一样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/b472a5b06f34/SaudiMedJ-43-7-751_page_3_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/7cf36d1be9fc/SaudiMedJ-43-7-751_page_2_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/c6bf71feae43/SaudiMedJ-43-7-751_page_2_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/b472a5b06f34/SaudiMedJ-43-7-751_page_3_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/7cf36d1be9fc/SaudiMedJ-43-7-751_page_2_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/c6bf71feae43/SaudiMedJ-43-7-751_page_2_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/118f/9749683/b472a5b06f34/SaudiMedJ-43-7-751_page_3_1.jpg

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本文引用的文献

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Amyloidosis in hidradenitis suppurativa: a cross-sectional study and review of the literature.化脓性汗腺炎中的淀粉样变性:一项横断面研究及文献复习。
Clin Exp Dermatol. 2020 Jul;45(5):565-571. doi: 10.1111/ced.14186. Epub 2020 Mar 25.
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Lymphedema in patients with hidradenitis suppurativa: a systematic review of published literature.化脓性汗腺炎患者的淋巴水肿:已发表文献的系统评价。
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Cutaneous squamous cell carcinoma complicating hidradenitis suppurativa: a review of the prevalence, pathogenesis, and treatment of this dreaded complication.
化脓性汗腺炎并发皮肤鳞状细胞癌:对这种可怕并发症的患病率、发病机制及治疗的综述
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AA amyloidosis: basic knowledge, unmet needs and future treatments.AA 淀粉样变性:基础知识、未满足的需求和未来的治疗方法。
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Hidradenitis suppurativa resulting in systemic amyloid A amyloidosis: a case report and review of the literature.化脓性汗腺炎导致系统性淀粉样蛋白A淀粉样变性:一例病例报告及文献复习
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