Patient with Jaundice, Dyspnea and Hyperferritinemia after COVID-19

V. R. Grechishnikova, P. Tkachenko, M. Zharkova, T. Nekrasova, V. Ivashkin
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Abstract

The aim: to highlight the importance of considering hemophagocytic lymphohistiocytosis in patients with jaundice of unclear origin and systemic inflammatory manifestations after coronavirus infection.Key points. A 64-y.o. patient was admitted to the hospital with jaundice, pruritus, fatigue, weight loss. The complaints occurred 2 weeks after discharge from the hospital for treatment of patients with coronavirus infection. Laboratory tests revealed signs of hepatic insufficiency, markers of cholestasis and inflammation persisted in time. Upon instrumental examination no signs of hepatosplenomegaly, biliary tree changes, intra- and extrahepatic obstruction were found. S. aureus was identified in blood cultures, CT scan of the facial skull bones showcased the focus of infection in the area of the roots of teeth 2.4 and 2.5. Therefore, antibiotics were prescribed. Subsequently, the patient's condition was complicated by the development of two episodes of acute respiratory distress syndrome, which occurred during the withdrawal of glucocorticosteroid therapy. Liver biopsy was performed, morphological study revealed signs of “vanishing bile duct” syndrome, excessive activation of macrophages and hemosiderosis of sinusoidal cells. Identified lesions can be found in hemophagocytic lymphohistiocytosis (HLH), a life-threatening complication of coronavirus infection. Glucocorticosteroids therapy, transfusions of human immunoglobulin, albumin, and parenteral nutrition have led to patient's condition improvement.Conclusion. COVID-19 provokes the development of secondary HLH 10 times more often than other respiratory viral infections. The possibility of hemophagocytic syndrome development should be considered, including cases of overlap syndrome with sepsis, in patients with unresolved jaundice, hyperferritinemia after coronavirus infection. Routinely used scales and criteria for diagnosis of HLH (H-score, HLH 2004) in such cases lacks sensitivity, therefore, careful analysis of clinical picture and exclusion of other causes of jaundice are required.
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新冠肺炎后黄疸、呼吸困难及高铁蛋白血症患者
目的:强调在冠状病毒感染后来源不明的黄疸和全身性炎症表现的患者中考虑噬血细胞淋巴组织细胞增多症的重要性。要点。64年有着专一。患者入院时伴有黄疸、瘙痒、乏力、体重减轻。投诉发生在收治冠状病毒感染患者出院后2周。实验室检查显示肝功能不全、胆汁淤积和炎症持续存在的迹象。仪器检查未发现肝脾肿大、胆道改变、肝内和肝外梗阻等征象。血培养中发现金黄色葡萄球菌,面部颅骨CT扫描显示感染的焦点在牙根2.4和2.5区域。因此,医生开了抗生素。随后,患者的病情因急性呼吸窘迫综合征的两次发作而复杂化,这两次发作发生在糖皮质激素治疗的停药期间。肝活检,形态学检查显示“胆管消失”综合征,巨噬细胞过度活化,窦细胞含铁血黄素沉着。可在噬血细胞性淋巴组织细胞增多症(HLH)中发现确诊病变,这是冠状病毒感染的一种危及生命的并发症。糖皮质激素治疗、输注人免疫球蛋白、白蛋白和肠外营养可使患者病情改善。COVID-19引发继发性HLH的频率是其他呼吸道病毒感染的10倍。冠状病毒感染后黄疸、高铁蛋白血症未解决的患者应考虑发生噬血细胞综合征的可能性,包括合并败血症的重叠综合征。在此类病例中,常规用于诊断HLH的量表和标准(H-score, HLH 2004)缺乏敏感性,因此需要仔细分析临床表现并排除黄疸的其他原因。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
44
审稿时长
8 weeks
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