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Severe complication during remission of Crohn’s disease: hemophagocytic lymphohistiocytosis due to acute cytomegalovirus infection

机译:缓解克罗恩病中的严重并发症:由于急性巨细胞病毒感染引起的血小杂淋巴管激瘤

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Introduction Immunosuppressive therapy is today’s standard treatment of patients with moderate to severe inflammatory bowel disease (IBD). The risk for opportunistic infections is increased due to this therapy and is a concern in the management of patient with IBD undergoing such a treatment. Case report In this paper, we describe a case of an acute cytomegalovirus (CMV) infection in a 35-year-old male patient with Crohn’s disease being in remission while receiving azathioprine therapy. His clinical presentation was high-grade fever, night sweats, skin rash, and abdominal pain.Laboratory findings showed pancytopenia, elevated liver enzymes, and high ferritin levels. Sonographic examination revealed splenomegaly and serological analysis proved an acute CMV infection. The severity of the acute illness and these results in the setting of immunosuppressive treatment with azathioprine were highly suspicious of hemophagocytic lymphohistiocytosis (HLH).Further investigations including bone marrow biopsy, analysis of natural killer cell function, and measurement of T-cell activity confirmed the suspected diagnosis. Treatment consisted of antiviral and symptomatic therapy. Discussion and conclusion HLH is a rare and severe condition triggered by uncontrolled stimulation of histiocytes and lymphocytes, resulting in abnormal cytokine production. The causes can be primary (genetic) or secondary due to acquired immunodeficiency or viral infections such as CMV. Several symptoms of this condition are unspecific, but the summary of clinical symptoms and signs are diagnostic. Treatment consists of specific intervention if possible and application of immunosuppressive drugs such as corticosteroids.
机译:引言免疫抑制治疗是今天对中度至重度炎症肠病(IBD)患者的标准治疗。由于这种疗法,机会感染的风险增加,并且是在进行这种治疗的IBD患者的患者中的关注。本文案例报告,我们描述了35岁的男性患者中急性胞嘧啶病毒(CMV)感染的情况,克罗恩病在接受Azathioprine治疗时受到缓解。他的临床介绍是高档发烧,盗汗,皮疹和腹痛。制造理因发现显示了韧身细胞增强,肝酶升高,铁素水平。超声检查显示脾肿大和血清学分析证明了急性CMV感染。急性疾病的严重程度和这些导致用氮杂唑的免疫抑制治疗的设置是高度可疑的血糖淋巴管引发症(HLH)。核心研究,包括骨髓活检,自然杀伤细胞功能分析,以及T细胞活性的测量证实了疑似诊断。治疗包括抗病毒和症状治疗。讨论和结论HLH是一种难以控制的组织细胞和淋巴细胞刺激引发的罕见和严重状态,导致细胞因子产生异常。由于获得的免疫缺陷或病毒感染如CMV,原因可以是原发性(遗传)或次要的原发性(遗传)或次要。这种情况的几种症状是无特异性的,但临床症状和标志的概要是诊断性的。如果可能的话,治疗包括特定干预,并施用免疫抑制药物如皮质类固醇。

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