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

被引:0
|
作者
Belisa, Telila K. [1 ]
Haile, Asteway M. [1 ]
Mesfin, Getinet B. [1 ]
Mengistie, Biruk T. [1 ]
Mengistie, Chernet T. [1 ]
Haile, Bezawit M. [2 ]
机构
[1] Addis Ababa Univ, Coll Hlth Sci, Sch Med, POB 9086, Addis Ababa, Ethiopia
[2] Addis Ababa Univ, Coll Hlth Sci, Dept Pediat & Child Hlth, Addis Ababa, Ethiopia
来源
IDCASES | 2024年 / 37卷
关键词
Hemophagocytic Lymphohistiocytosis(HLH); Visceral Leishmaniasis(VL); Toddler; Case report; MACROPHAGE ACTIVATION SYNDROME; DIAGNOSIS; ADULT;
D O I
10.1016/j.idcr.2024.e02059
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
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 degrees C), tachypnea (70 breaths/min), tachycardia (132 beats/min), pallor, and hepatosplenomegaly. Initial investigation revealed leukopenia (2240/mu l), anemia (7.3 g/dl), and severe thrombocytopenia (26,000/ mu l). 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.
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