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移植受者中由链格孢属物种引起的暗色丝孢霉病。

Phaeohyphomycosis due to Alternaria species in transplant recipients.

作者信息

Boyce R D, Deziel P J, Otley C C, Wilhelm M P, Eid A J, Wengenack N L, Razonable R R

机构信息

Division of Infectious Diseases, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

出版信息

Transpl Infect Dis. 2010 Jun;12(3):242-50. doi: 10.1111/j.1399-3062.2009.00482.x. Epub 2009 Dec 9.

Abstract

Alternaria species are members of a heterogeneous group of dematiaceous fungi that rarely cause opportunistic infections in transplant recipients. During a 20-year period from 1989 to 2008, 8 solid organ transplant recipients (63% males; median age, 48 years) developed Alternaria species infections at the Mayo Clinic. All patients were highly immunocompromised as evidenced by their receipt of multiple transplants, treatment of acute and chronic allograft rejection, and occurrence of other opportunistic infections. All patients presented with non-tender erythematous or violaceous skin papules, nodules, or pustules in exposed areas of the extremities. No case of visceral dissemination was observed. Itraconazole was the most common drug used for treatment, although voriconazole, posaconazole, and caspofungin could potentially be useful based on our limited clinical data and in vitro antifungal susceptibility testing. One patient was treated with voriconazole, while another patient who was refractory to itraconazole had rapid resolution of lesions after the addition of caspofungin. Attempts at antifungal therapy alone were unsuccessful; all patients eventually required surgical excision of lesions. In conclusion, Alternaria species are rare but increasingly recognized opportunistic infections among highly immunocompromised transplant recipients. Wide excisional surgery combined with prolonged systemic antifungal therapy and reduction in immunosuppressive regimens provided the best chance of cure. Although itraconazole remains the most common drug for treatment, this case series highlights the potential clinical utility of caspofungin, voriconazole, and posaconazole as alternative regimens.

摘要

链格孢属真菌是一群异质性的暗色真菌,很少在移植受者中引起机会性感染。在1989年至2008年的20年期间,梅奥诊所的8名实体器官移植受者(63%为男性;中位年龄48岁)发生了链格孢属真菌感染。所有患者均高度免疫受损,这从他们接受多次移植、治疗急性和慢性移植物排斥反应以及发生其他机会性感染可以得到证明。所有患者在四肢暴露部位均出现无痛性红斑或紫红色皮肤丘疹、结节或脓疱。未观察到内脏播散病例。伊曲康唑是最常用的治疗药物,尽管根据我们有限的临床数据和体外抗真菌药敏试验,伏立康唑、泊沙康唑和卡泊芬净可能也有用。一名患者接受了伏立康唑治疗,而另一名对伊曲康唑耐药的患者在加用卡泊芬净后皮损迅速消退。单独的抗真菌治疗尝试均未成功;所有患者最终都需要手术切除皮损。总之,链格孢属真菌在高度免疫受损的移植受者中是罕见但越来越被认识到的机会性感染。广泛的切除手术联合延长的全身抗真菌治疗以及减少免疫抑制方案提供了最佳的治愈机会。尽管伊曲康唑仍然是最常用的治疗药物,但该病例系列突出了卡泊芬净、伏立康唑和泊沙康唑作为替代方案的潜在临床效用。

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