肾移植受者常见热带传染病的罕见并发症--病例报告。

IF 0.8 Q4 UROLOGY & NEPHROLOGY
Indian Journal of Nephrology Pub Date : 2024-01-01 Epub Date: 2023-03-08 DOI:10.4103/ijn.ijn_252_22
Mythri Shankar, Sreedhara C Gurusiddiah, Monika Nayaka, Kishan Aralapuram
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引用次数: 0

摘要

嗜血细胞淋巴组织细胞增多症(HLH)是一种罕见的、危及生命的疾病,是由于广泛的、不受控制的免疫激活引起的。有关肾移植受者 HLH 的文献很少。我们报告了一例 27 岁男性肾移植受者的病例,他出现登革热和急性同种异体移植功能障碍。经支持治疗后,他的异体移植功能有所改善,但发现他的全血细胞减少症恶化,血清铁蛋白水平异常升高。因泛血细胞减少而进行的骨髓穿刺发现了嗜血细胞增多症。根据改良的 HLH 诊断标准(2009 年),他被诊断为登革热病毒感染继发 HLH。他接受了支持治疗和类固醇治疗,出院时病情稳定,肾移植功能正常。据我们所知,这是首例肾移植受者因登革病毒感染继发 HLH,经及时诊断和适当治疗后成功治愈的病例报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Uncommon Complication of a Common Tropical Infection in a Kidney Transplant Recipient - A Case Report.

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening condition due to extensive and uncontrolled immune activation. There is sparse literature on HLH in kidney transplant recipients. We report a case of a 27-year -old male kidney transplant recipient who presented with dengue fever and acute allograft dysfunction. Following improvement in allograft function with supportive treatment, he was found to have worsening pancytopenia with unusually high serum ferritin levels. Bone marrow aspiration performed for pancytopenia revealed hemophagocytosis. A diagnosis of HLH secondary to dengue viral infection was made based on the modified HLH diagnostic criteria (2009). He received supportive treatment and steroids and was discharged in a stable condition with normal kidney allograft functions. To our knowledge, this is the first case report of HLH secondary to dengue viral infection in a kidney allograft recipient managed successfully with timely diagnosis and appropriate treatment.

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来源期刊
Indian Journal of Nephrology
Indian Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
1.40
自引率
0.00%
发文量
128
审稿时长
24 weeks
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