Hemophagocytic lymphohistiocytosis syndrome (HLH) in HIV-associated Kaposi sarcoma patients: The first case series from a single center in Türkiye.

IF 1.3 4区 医学 Q4 IMMUNOLOGY
Zarifa Orta, Aysun Benli, Arif Atahan Çağatay, Seniha Başaran, Simge Erdem, Sevgi Beşişik
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引用次数: 0

Abstract

BackgroundKaposi sarcoma in people living with HIV and AIDS usually involves slowly progressive skin lesions. Cases of Kaposi sarcoma complicated by hemophagocytic lymphohistiocytosis are rare. In this report, we present the first series of hemophagocytic lymphohistiocytosis cases from Türkiye associated with AIDS and Kaposi sarcoma.MethodsCases of hemophagocytic lymphohistiocytosis in people living with HIV and AIDS and Kaposi sarcoma who met the HLH-2004 diagnostic criteria recommended by the "Histiocyte Society" were included in the study. The patient's demographic, clinical, and laboratory characteristics were recorded retrospectively.ResultsFour patients presented with fever, cytopenia, peripheral lymphadenomegaly, splenomegaly, and hepatomegaly. Fever persisted throughout their hospitalization. At the time of HLH diagnosis, Kaposi sarcoma was detected in the lymph node biopsies of one patient and in the skin biopsies of three patients. Hemophagocytosis was observed in bone marrow aspirations from all patients. Three patients received dexamethasone and etoposide for hemophagocytic lymphohistiocytosis treatment, while one received dexamethasone alone. All four patients died.ConclusionsCases of hemophagocytic lymphohistiocytosis associated with Kaposi sarcoma and AIDS are rare in the literature. In conclusion, high fever may appear in the early stages of Kaposi sarcoma in people living with HIV and AIDS. Since hemophagocytic lymphohistiocytosis has a high mortality rate, early diagnosis and prompt initiation of appropriate treatment are crucial.

hiv相关卡波西肉瘤患者的噬血细胞淋巴组织细胞增多综合征(HLH):来自 rkiye单一中心的第一个病例系列。
艾滋病毒和艾滋病感染者的卡波西肉瘤通常涉及缓慢进展的皮肤病变。卡波西肉瘤合并噬血细胞性淋巴组织细胞增多症是罕见的。在本报告中,我们报告了首例与艾滋病和卡波西肉瘤相关的基耶氏病患者的噬血细胞性淋巴组织细胞增多症。方法选取符合“组织细胞学会”推荐的HLH-2004诊断标准的HIV / AIDS感染者和卡波西肉瘤患者的噬血细胞性淋巴组织细胞增多症病例作为研究对象。回顾性记录患者的人口学、临床和实验室特征。结果4例患者表现为发热、细胞减少、周围淋巴肿大、脾肿大、肝肿大。他们住院期间一直发烧。在诊断HLH时,在1例患者的淋巴结活检和3例患者的皮肤活检中检测到卡波西肉瘤。所有患者骨髓穿刺均出现噬血细胞现象。3例患者接受地塞米松联合依托泊苷治疗噬血细胞淋巴组织细胞增多症,1例患者单独接受地塞米松治疗。4名患者全部死亡。结论卡波西肉瘤合并艾滋病合并嗜血球淋巴组织细胞增多症的病例文献罕见。总之,艾滋病毒和艾滋病感染者在卡波西肉瘤的早期阶段可能出现高烧。由于噬血细胞淋巴组织细胞病死亡率高,早期诊断和及时开始适当治疗至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.60
自引率
7.10%
发文量
144
审稿时长
3-6 weeks
期刊介绍: The International Journal of STD & AIDS provides a clinically oriented forum for investigating and treating sexually transmissible infections, HIV and AIDS. Publishing original research and practical papers, the journal contains in-depth review articles, short papers, case reports, audit reports, CPD papers and a lively correspondence column. This journal is a member of the Committee on Publication Ethics (COPE).
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