Severe hemophagocytic lymphohistiocytosis secondary to disseminated histoplasmosis in a patient with HIV/AIDS: a case report.

IF 1.7 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-05-12 eCollection Date: 2025-06-01 DOI:10.1097/MS9.0000000000003350
Dipesh Kumar Rohita, Karun Bhattarai, Jigyanshu Adhikari, Ali Usama, Anees Cheema, Anubhav Poudel, Prakash Poudel, Zin Hinn Phyu, Abeera W Rabbani, Zeyar Thet
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Abstract

Introduction and importance: Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening disorder marked by immune system dysregulation, leading to a severe inflammatory response that can affect multiple organs. It can be triggered by infections, and HLH secondary to disseminated histoplasmosis remains poorly understood, with uncertain guidelines on immunosuppressive therapy. Early diagnosis and prompt treatment are critical in preventing fatal outcomes, but challenges in diagnosis complicate this process, particularly in immunocompromised patients.

Case presentation: A 51-year-old immunocompromised woman with asthma, gastritis, and anemia presented with fever, malaise, weight loss, and respiratory symptoms. Initial workup revealed pancytopenia, elevated ferritin levels, and an HIV diagnosis with a low CD4 count. Suspecting HLH, she was treated with antiretrovirals, antifungals, and steroids. Her condition worsened, and she developed MRSA sepsis, metabolic acidosis, and multiorgan failure. Histoplasmosis was confirmed, and treatment with liposomal amphotericin B was initiated. Unfortunately, she suffered a cardiac arrest and died on day 11. Postmortem findings confirmed disseminated histoplasmosis-induced HLH.

Clinical discussion: HLH is a rare but severe immune activation disorder causing systemic inflammation, multi-organ failure, and high mortality. It can be primary (genetic) or secondary. Diagnosis follows HLH-2004 criteria, and treatment includes immunosuppressive therapy and hematopoietic cell transplantation.

Conclusion: This case illustrates the complexities of diagnosing HLH in immunocompromised patients. Delays in obtaining critical lab results and initiating treatment contributed to the patient's rapid deterioration. Early intervention and careful monitoring are crucial in managing such complex cases, where timely diagnosis can significantly impact patient outcomes.

HIV/AIDS患者继发于播散性组织浆菌病的严重噬血细胞淋巴组织细胞增多症1例报告。
简介及重要性:噬血细胞性淋巴组织细胞增多症(HLH)是一种以免疫系统失调为特征的危及生命的疾病,可导致严重的炎症反应,影响多个器官。它可以由感染引发,而继发于播散性组织胞浆菌病的HLH仍然知之甚少,免疫抑制治疗的指导方针也不确定。早期诊断和及时治疗对于预防致命后果至关重要,但诊断方面的挑战使这一过程复杂化,特别是在免疫功能低下的患者中。病例介绍:51岁免疫功能低下女性,伴哮喘、胃炎和贫血,表现为发热、不适、体重减轻和呼吸道症状。最初的检查显示全血细胞减少症,铁蛋白水平升高,CD4计数低的HIV诊断。由于怀疑患有HLH,她接受了抗逆转录病毒药物、抗真菌药物和类固醇治疗。她的病情恶化,出现了MRSA败血症、代谢性酸中毒和多器官衰竭。确诊为组织胞浆菌病,并开始用两性霉素B脂质体治疗。不幸的是,她心脏骤停,于第11天去世。尸检结果证实播散性组织胞浆菌引起的HLH。临床讨论:HLH是一种罕见但严重的免疫激活障碍,引起全身炎症,多器官衰竭和高死亡率。它可以是原发性(遗传)或继发性。诊断遵循HLH-2004标准,治疗包括免疫抑制治疗和造血细胞移植。结论:本病例说明了在免疫功能低下患者中诊断HLH的复杂性。在获得关键实验室结果和开始治疗方面的延误导致了患者的迅速恶化。早期干预和仔细监测对于处理此类复杂病例至关重要,及时诊断可显著影响患者的预后。
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
Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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5.90%
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