一例接受免疫抑制治疗的溃疡性结肠炎患者全身性猫抓病。

IF 3.8 Q2 INFECTIOUS DISEASES Therapeutic Advances in Infectious Disease Pub Date : 2024-11-08 eCollection Date: 2024-01-01 DOI:10.1177/20499361241271832
Bruna Rošić Despalatović, Andre Bratanić, Dora Božić, Katarina Vilović, Nenad Kunac, Žarko Ardalić
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引用次数: 0

摘要

猫抓病(CSD)是一种人畜共患病,通常通过抓伤或咬伤传播给人类。主要致病菌是鸡巴顿氏菌。它可引起轻微的自限性疾病。在免疫力低下的患者中,由于抗菌反应受到抑制,感染过程可能会更加严重,导致危及生命的疾病。一名 54 岁的男性患者患有溃疡性结肠炎。在接受首剂英夫利昔单抗 400 毫克静脉注射和 0.5 毫克/千克甲基强的松龙治疗 5 天后,他出现了腋窝淋巴结肿大和腹腔内淋巴结肿大,并伴有猫咬伤后由鸡球菌引起的肝内肿块。经过多种抗生素和泼尼松龙的长期治疗,患者的临床症状有所好转,肝脏和腹腔内淋巴结也有所消退。在进一步治疗溃疡性结肠炎后,我们评估了重新采用免疫抑制疗法的可能性。在咨询传染病专家后,我们引入了阿达木单抗。在复诊时,患者的溃疡性结肠炎已得到缓解,也没有巴顿菌病再活化的迹象。CSD 等疾病的临床表现和预后都是良性的,但在免疫力低下的患者中却可能发展成严重的危及生命的病程。这就需要对此类患者的免疫过程有一个复杂的了解,而在成功治疗 CSD 后重新采用免疫抑制疗法可能并不会增加再激活的风险。
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A case of generalized cat scratch disease in a patient with ulcerative colitis on immunosuppressive therapy.

Cat scratch disease (CSD) is a zoonotic disease transmitted to humans, usually via scratches or bites. Bartonella henselae is the primary causative agent. It causes a mild, self-limiting disease. In immunocompromised patients, the course of the infection can be more serious because of the suppressed antibacterial response, causing a life-threatening disease. A 54-year-old male patient presented with ulcerative colitis. Five days after receiving the first dose of infliximab 400 mg intravenously and 0.5 mg/kg methylprednisolone, he presented with enlarged axillary lymph nodes and colliquation of the intraabdominal lymph node with intrahepatic colliquating areas caused by B. henselae after cat bites. Long-term treatment with multiple antibiotics and prednisolone resulted in clinical improvement and regression of the liver and intra-abdominal lymph nodes. After further treatment for ulcerative colitis, we assessed the possibility of reintroducing immunosuppressive therapy. Adalimumab was introduced after consulting an infectious disease specialist. At the follow-up visit, the patient was in remission of ulcerative colitis and without signs of reactivation of bartonellosis. Diseases such as CSD with a benign clinical appearance and prognosis can develop a severe and life-threatening course in immunocompromised patients. This requires a complex understanding of the immune processes in such patients, and the reintroduction of immunosuppressive therapy after successful treatment of CSD probably does not increase the risk of reactivation.

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来源期刊
CiteScore
5.30
自引率
8.80%
发文量
64
审稿时长
9 weeks
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