Xia X J, Shen H, Liu Z H
Department of Dermatology, Third Hospital of Hangzhou, Hangzhou, China.
Clin Exp Dermatol. 2015 Dec;40(8):875-8. doi: 10.1111/ced.12642. Epub 2015 Mar 25.
We describe a case of primary cutaneous mucormycosis in a 44-year-old man with an 18-month history of infiltrative erythematous plaques and haemorrhagic crusting on the dorsum of his left hand. The isolate was identified as Mucor irregularis (formerly Rhizomucor variabilis) based on the fungus morphology and DNA sequencing results. Improvement was observed after a 6-month treatment course of itraconazole. No recrudescence was seen during a follow-up of 23 months after treatment.
我们描述了一例44岁男性原发性皮肤毛霉病病例，该患者左手背部有18个月的浸润性红斑斑块和出血性结痂病史。根据真菌形态学和DNA测序结果，分离株被鉴定为不规则毛霉（以前称为多变根毛霉）。在接受6个月的伊曲康唑治疗后观察到病情改善。治疗后23个月的随访期间未见复发。
