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一名接受鲁索替尼治疗的原发性骨髓纤维化患者发生肺隐球菌病。

Pulmonary cryptococcosis in a ruxolitinib-treated patient with primary myelofibrosis.

作者信息

Hirano Anna, Yamasaki Masahiro, Saito Naomi, Iwato Koji, Daido Wakako, Funaishi Kunihiko, Ishiyama Sayaka, Deguchi Naoko, Taniwaki Masaya, Ohashi Nobuyuki

机构信息

Department of Respiratory Disease, Hiroshima Red Cross Hospital & Atomic Bomb Survivors Hospital, 1-9-6 Senda-machi, Naka-ku, Hiroshima 730-8619, Japan.

Department of Blood Transfusion, Hiroshima Red Cross Hospital & Atomic Bomb Survivors Hospital, 1-9-6 Senda-machi, Naka-ku, Hiroshima 730-8619, Japan.

出版信息

Respir Med Case Rep. 2017 Jul 4;22:87-90. doi: 10.1016/j.rmcr.2017.06.015. eCollection 2017.

Abstract

We present the case of a 79-year-old man who showed multiple pulmonary nodules on chest computed tomography (CT) after being treated for 6 months with ruxolitinib, an inhibitor of Janus kinase (JAK) 1 and 2, to treat primary myelofibrosis. We examined the lesions by bronchoscopy, and the biopsy specimen revealed fungus bodies of with granulomatous inflammation. As a result, the patient was diagnosed with pulmonary cryptococcosis. The patient was treated with fluconazole (200 mg daily for 2 weeks) with concomitant ruxolitinib administration, but the pulmonary lesions progressed. Subsequently, the patient was treated with voriconazole (300 mg daily for 3 weeks), but the lesions worsened further. The administration of ruxolitinib was therefore discontinued, and the dosage of voriconazole was increased to 400 mg daily. Three months later, the pulmonary lesions diminished in size. The present case of pulmonary cryptococcosis occurred in a patient treated with ruxolitinib. Treatment of pulmonary cryptococcosis with concomitant JAK inhibitor administration may result in poor treatment efficacy. It might be better to stop administration of JAK inhibitors, if possible, in patients being treated for pulmonary cryptococcosis.

摘要

我们报告了一例79岁男性患者的病例,该患者在使用鲁索替尼(一种Janus激酶(JAK)1和2抑制剂)治疗原发性骨髓纤维化6个月后,胸部计算机断层扫描(CT)显示有多个肺结节。我们通过支气管镜检查了这些病变,活检标本显示有真菌体伴肉芽肿性炎症。结果,该患者被诊断为肺隐球菌病。患者接受氟康唑治疗(每日200 mg,共2周),同时继续使用鲁索替尼,但肺部病变仍进展。随后,患者接受伏立康唑治疗(每日300 mg,共3周),但病变进一步恶化。因此停用了鲁索替尼,并将伏立康唑剂量增加至每日400 mg。三个月后,肺部病变尺寸减小。本病例的肺隐球菌病发生在一名接受鲁索替尼治疗的患者身上。同时使用JAK抑制剂治疗肺隐球菌病可能导致治疗效果不佳。对于正在接受肺隐球菌病治疗的患者,如果可能的话,停用JAK抑制剂可能更好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da65/5499110/f970ee2b618a/gr1.jpg

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