Hemophagocytic lymphohistiocytosis secondary to visceral leishmaniasis: A case report of a rare complication of visceral leishmaniasis

IF 1.1 Q4 INFECTIOUS DISEASES
IDCases Pub Date : 2024-01-01 DOI:10.1016/j.idcr.2024.e02059
Telila K. Belisa , Asteway M. Haile , Getinet B. Mesfin , Biruk T. Mengistie , Chernet T. Mengistie , Bezawit M. Haile
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Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a rare, potentially life-threatening clinical syndrome characterized by hyperactivation of inflammatory mediators and harmful end-organ damage. Visceral leishmaniasis (VL)-induced HLH is a rare disease with significant diagnostic and management implications. Herein, we present a case of secondary HLH as a complication of visceral leishmaniasis in a two-year-old toddler. A 2-year-old male toddler was admitted for evaluation of a prolonged 4-week fever. Accompanying the fever, he developed progressive abdominal swelling, intermittent bilateral nasal bleeding, and repeated chest-focus infections of similar duration. The patient was acutely sick, with chronic signs of malnutrition (mid-upper arm circumference of 10.5 cm), fever (39 °C), tachypnea (70 breaths/min), tachycardia (132 beats/min), pallor, and hepatosplenomegaly. Initial investigation revealed leukopenia (2240/μl), anemia (7.3 g/dl), and severe thrombocytopenia (26,000/μl). With consideration of febrile neutropenia, the patient was started on cefepime with further revision to vancomycin and meropenem based on the culture result. After 10 days of persistent fever and poor clinical condition, an immunochromatographic rapid test with the rK39 antigen was conducted, and the patient was found to be positive for Leishmania spp. Intravenous liposomal amphotericin B (AmBisome) was initiated. On the 6th day of treatment, the patient’s clinical and laboratory profiles severely deteriorated, and further laboratory investigation showed elevated triglyceride (524 mg/dl) and ferritin levels (1500 ng/mL). VL-induced secondary HLH was confirmed, and intravenous dexamethasone was initiated. Subsequently, his clinical and laboratory findings significantly improved, and he was discharged with PO dexamethasone. Our case highlights the intricate nature of VL-induced HLH and the need for high index of suspicion and timely management.

继发于内脏利什曼病的嗜血细胞淋巴组织细胞增多症:内脏利什曼病罕见并发症的病例报告
嗜血细胞淋巴组织细胞增多症(HLH)是一种罕见的、可能危及生命的临床综合征,其特点是炎症介质过度激活和有害的内脏器官损伤。内脏利什曼病(VL)诱发的 HLH 是一种罕见疾病,对诊断和治疗具有重要意义。在此,我们介绍一例两岁幼儿因内脏利什曼病并发继发性 HLH 的病例。一名 2 岁男性幼儿因持续 4 周发烧入院评估。在发热的同时,他还出现了进行性腹部肿胀、间歇性双侧鼻出血以及持续时间相似的反复胸腔灶感染。患者急性发病,长期营养不良(中上臂围 10.5 厘米)、发热(39 °C)、呼吸急促(70 次/分)、心动过速(132 次/分)、面色苍白和肝脾肿大。初步检查发现白细胞减少(2240/μl)、贫血(7.3 g/dl)和严重血小板减少(26000/μl)。考虑到发热性中性粒细胞减少症,患者开始使用头孢吡肟,并根据培养结果进一步改用万古霉素和美罗培南。在持续发热和临床状况不佳的 10 天后,对患者进行了 rK39 抗原免疫层析快速检测,结果显示利什曼原虫阳性。治疗第 6 天,患者的临床和实验室检查结果严重恶化,进一步的实验室检查显示甘油三酯(524 mg/dl)和铁蛋白水平升高(1500 ng/mL)。证实VL诱发继发性HLH,并开始静脉注射地塞米松。随后,他的临床和实验室检查结果明显好转,并在服用地塞米松后出院。我们的病例凸显了 VL 诱导的 HLH 的复杂性,以及高度怀疑和及时处理的必要性。
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来源期刊
IDCases
IDCases INFECTIOUS DISEASES-
CiteScore
2.60
自引率
6.70%
发文量
300
审稿时长
10 weeks
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