[嗜血细胞性淋巴组织细胞增生症(secondary hemophagocytic lymphohistiocytosis),由冰冻型钩端螺旋体病引起,伴有急性肾功能衰竭。

Deutsche medizinische Wochenschrift (1946) Pub Date : 2025-04-01 Epub Date: 2025-03-31 DOI:10.1055/a-2455-6902
Marvin Dumke, Nadine Wilsdorf, Iris Barndt
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引用次数: 0

摘要

患者51岁,以发热、上腹痛、用力性呼吸困难为主要表现。血流动力学不稳定,伴全身性黄疸,肝脾肿大,麻疹样皮疹伴瘀斑及双侧结膜炎。实验室结果显示c反应蛋白和降钙素原升高,以及全血细胞减少症和高胆红素血症。此外,还发现高甘油三酯血症、高铁蛋白血症和可溶性il -2受体升高。传染病检测检测钩端螺旋体igm抗体。骨髓细胞学表现为噬血细胞增多。诊断为黄疸钩端螺旋体病继发性噬血细胞淋巴组织细胞增多症。立即开始抗生素治疗和液体和血管加压剂循环支持,无创通气和血液透析稳定了患者。使用类固醇和多价免疫球蛋白后,器官功能恢复。噬血细胞性淋巴组织细胞增多症是脓毒症的重要鉴别诊断或伴随诊断,可由钩端螺旋体病等罕见诊断的感染性诱发因素引起。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Secondary hemophagocytic lymphohistiocytosis due to icteric leptospirosis with acute renal failure].

A 51-year-old patient presented himself with fever, upper abdominal pain and exertional dyspnea. Hemodynamic instability accompanied by generalized icterus, hepatosplenomegaly, a morbilliform rash with petechia and bilateral conjunctivitis revealed in clinical examination.Laboratory results revealed elevated C-reactive protein and procalcitonin as well as pancytopenia and hyperbilirubinemia. Furthermore hypertriglyceridemia, hyperferritinemia and elevated soluble IL-2-receptor were found. Testing for infectious diseases detected IgM-antibodies to leptospires. Bone marrow cytology featured hemophagocytosis.Secondary hemophagocytic lymphohistiocytosis due to icteric leptospirosis (Weil's disease) was diagnosed.Immediate antibiotic therapy and circulatory support by fluid and vasopressors was initiated and non-invasive ventilation and hemodialysis stabilized the patient. With steroids and polyvalent immunoglobulins the organ functions recovered.Hemophagocytic lymphohistiocytosis is an important differential or concomitant diagnosis in sepsis and can be induced by rarely diagnosed infectious triggers like leptospirosis.

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