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Simultaneous development of sarcoidosis and cutaneous vasculitis in a patient with refractory Crohn’s disease during infliximab therapy

机译:英夫利昔单抗治疗期间难治性克罗恩病患者同时出现结节病和皮肤血管炎

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Paradoxical inflammations during anti-TNF-α therapy are defined as adverse effects such as psoriasiform skin lesions, uveitis and sarcoidosis-like granulomas induced by immune reactions, not by infectious agents. Here, we report a very rare case of the simultaneous development of sarcoidosis and cutaneous vasculitis in a patient with refractory Crohn’s disease during infliximab therapy and both of which resolved spontaneously without the cessation of infliximab. In September 2000, 23-year old Japanese male was diagnosed with Crohn’s disease. Prednisolone in combination with mesalazine was introduced at first and succeeded for almost one year. In June 2002, since his gastrointestinal symptoms relapsed and were refractory, infliximab (IFX) therapy 5?mg/kg was introduced. In February 2011, because he had repeated arthralgia almost every intravenous IFX administration, IFX was increased to 10?mg/kg under the diagnosis of a secondary failure of IFX. In December 2012, he complained of slight dry cough and an itchy eruption on both lower limbs, and he was referred to our hospital due to the appearance of bilateral hilar lymphadenopathy on chest X-ray examination. Chest computed tomogram revealed bilateral hilar lymphadenopathy and fine reticulonodular shadows on the bilateral upper lungs. Serum calcium, angiotensin-converting enzyme and soluble interleukin 2 receptor levels were not elevated, but the titer of antinuclear antibody was considerably elevated. Mycobacterium infection was carefully excluded. Trans-bronchial lung biopsy showed non-caseating epithelioid cell granulomas compatible with sarcoidosis. The skin biopsy of the right limb was diagnosed as leukocytoclastic vasculitis. The patient was diagnosed as having a series of paradoxical inflammations during anti-TNF-α therapy. Since his paradoxical inflammations were not severe and opportunistic infections were excluded, IFX was cautiously continued for refractory Crohn’s disease. Nine months later, not only his intrathoracic lesions but also his cutaneous lesions had spontaneously resolved. Physicians caring for patients with anti-TNF-α therapy should know that, based on a careful exclusion of infectious agents and thoughtful assessment of the patient’s possible risks and benefits, paradoxical inflammations can be resolved without the cessation of anti-TNF-α therapy.
机译:抗TNF-α治疗期间的自相矛盾的炎症定义为不良反应,例如由免疫反应而非传染源引起的牛皮癣样皮肤病变,葡萄膜炎和结节病样肉芽肿。在这里,我们报道了在英夫利昔单抗治疗期间难治性克罗恩病患者同时发生结节病和皮肤血管炎的罕见情况,这两种病都能自发缓解而无需终止英夫利昔单抗。 2000年9月,一名23岁的日本男性被诊断出患有克罗恩病。刚开始使用泼尼松龙与美沙拉嗪的组合,并成功使用了近一年。 2002年6月,由于他的胃肠道症状复发并且变得难治,因此引入了英夫利昔单抗(IFX)治疗5?mg / kg。在2011年2月,由于他几乎每次静脉注射IFX都会重复关节痛,因此在诊断出IFX继发性衰竭后,IFX增至10?mg / kg。 2012年12月,他主诉双下肢轻度咳嗽和发痒,由于胸部X光检查发现双侧肺门淋巴结肿大,他被转诊至我院。胸部计算机断层扫描显示双侧肺门淋巴结肿大,双侧上肺部有细网状阴影。血清钙,血管紧张素转换酶和可溶性白介素2受体水平未升高,但抗核抗体的效价却显着升高。仔细排除了分枝杆菌感染。经支气管肺活检显示与结节病相容的非干酪样上皮样细胞肉芽肿。右肢皮肤活检被诊断为白细胞碎裂性血管炎。患者在抗TNF-α治疗期间被诊断出患有一系列矛盾的炎症。由于他的自相矛盾的炎症并不严重,并且排除了机会性感染,因此对于难治的克罗恩病,IFX仍谨慎使用。九个月后,不仅他的胸腔内病变,而且他的皮肤病变均自发消退。照顾抗TNF-α疗法的医师应了解,基于仔细排除传染源并仔细评估患者可能的风险和益处,可以在不停止抗TNF-α疗法的情况下解决矛盾的炎症。

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