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Hemophagocytic lymphohistiocytosis: review of etiologies and management.噬血细胞性淋巴组织细胞增生症:病因及治疗综述
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Reactive hemophagocytic syndrome in adults: a retrospective analysis of 162 patients.成人反应性噬血细胞综合征:162 例回顾性分析。
Am J Med. 2014 Nov;127(11):1118-1125. doi: 10.1016/j.amjmed.2014.04.034. Epub 2014 May 14.
3
Review of haemophagocytic lymphohistiocytosis.噬血细胞性淋巴组织细胞增生症综述。
Arch Dis Child. 2011 Jul;96(7):688-93. doi: 10.1136/adc.2009.176610. Epub 2010 Jun 28.
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Hemophagocytic syndromes.噬血细胞综合征
Blood Rev. 2007 Sep;21(5):245-53. doi: 10.1016/j.blre.2007.05.001. Epub 2007 Jun 21.
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Familial and acquired hemophagocytic lymphohistiocytosis.家族性和获得性噬血细胞性淋巴组织细胞增生症。
Eur J Pediatr. 2007 Feb;166(2):95-109. doi: 10.1007/s00431-006-0258-1. Epub 2006 Dec 7.
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[Hemophagocytic syndrome].噬血细胞综合征
Rev Med Interne. 2002 Sep;23(9):768-78. doi: 10.1016/s0248-8663(02)00673-2.
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Hemophagocytic syndrome in the critically ill.危重症患者的噬血细胞综合征
Intensive Care Med. 2001 May;27(5):948-9. doi: 10.1007/s001340100925.
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Requirement for etoposide in the treatment of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.依托泊苷在治疗爱泼斯坦-巴尔病毒相关噬血细胞性淋巴组织细胞增生症中的应用需求。
J Clin Oncol. 2001 May 15;19(10):2665-73. doi: 10.1200/JCO.2001.19.10.2665.
9
Familial hemophagocytic lymphohistiocytosis and viral infections.家族性噬血细胞性淋巴组织细胞增生症与病毒感染
Acta Paediatr. 1993 Apr;82(4):369-72. doi: 10.1111/j.1651-2227.1993.tb12699.x.
10
Diagnostic guidelines for hemophagocytic lymphohistiocytosis. The FHL Study Group of the Histiocyte Society.噬血细胞性淋巴组织细胞增生症诊断指南。组织细胞协会FHL研究组
Semin Oncol. 1991 Feb;18(1):29-33.

一种罕见的逆行性肾内手术并发症:噬血细胞综合征。

A Rare Retrograde Intrarenal Surgery Complication: Hemophagocytic Syndrome.

作者信息

Akgül Murat, Yazıcı Cenk, Ateş Hüseyin, Altın Enes, Turgut Burhan

机构信息

Urology Department and Faculty of Medicine, Tekirdağ Namık Kemal University, Tekirdağ, Turkey.

Hematology Department, Faculty of Medicine, Tekirdağ Namık Kemal University, Tekirdağ, Turkey.

出版信息

J Endourol Case Rep. 2020 Dec 29;6(4):339-342. doi: 10.1089/cren.2020.0066. eCollection 2020.

DOI:10.1089/cren.2020.0066
PMID:33457669
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7803215/
Abstract

Hemophagocytic syndrome (HS) is a syndromic complex that is categorized in the group of histiocytic disorders associated with macrophages. A 39-year-old male patient was admitted to the outpatient clinic with complaint of left flank pain. A 1 cm kidney stone was found in the upper pole of left kidney at radiologic imaging. The patient underwent retrograde intrarenal surgery (RIRS) with no peroperative complication. High fever and increasing of acute-phase reactants were observed at postoperative first day. Besides resistant fever, pancytopenia developed despite the appropriate antibiotherapy. The urine and blood cultures were sterile. After multidisciplinary consultation, bone marrow sampling was performed. Microscopic examination of the bone marrow material revealed that the macrophage cells phagocyted the erythrocytes, which was compatible with HS. Unfortunately despite the appropriate medical HS treatment, the patient died due to multiorgan failure at the 21st day of RIRS. HS is a significantly rare complication after RIRS, which was presented initially with postoperative fever. HS should be kept in mind if the patient had resistant fever and pancytopenia despite the appropriate antibiotherapy.

摘要

噬血细胞综合征(HS)是一种综合征性复合体,归类于与巨噬细胞相关的组织细胞疾病组。一名39岁男性患者因左侧腰痛主诉入住门诊。影像学检查发现左肾上极有一枚1厘米的肾结石。患者接受了逆行肾内手术(RIRS),术中无并发症。术后第一天观察到高热和急性期反应物增加。除了持续性发热外,尽管进行了适当的抗生素治疗,仍出现了全血细胞减少。尿液和血液培养均无菌。经过多学科会诊后,进行了骨髓采样。骨髓材料的显微镜检查显示巨噬细胞吞噬了红细胞,这与HS相符。不幸的是,尽管对HS进行了适当的药物治疗,但患者在RIRS术后第21天因多器官衰竭死亡。HS是RIRS术后一种极为罕见的并发症,最初表现为术后发热。如果患者在接受适当的抗生素治疗后仍有持续性发热和全血细胞减少,应考虑HS。