Li Fang-Gu, Yang Yan-Ping, Li Wei, Sheng Ping, Li Wen, Huang Wen-Ming, Fan Yi-Ming
Department of Dermatology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, 524001, Guangdong, China.
Mycopathologia. 2017 Jun;182(5-6):561-567. doi: 10.1007/s11046-016-0103-7. Epub 2017 Jan 10.
To date, only one case of post-traumatic endophthalmitis caused by Scedosporium dehoogii has been reported, but its contamination or colonization might not be precluded due to the absence of pathogenic isolation and/or pathological examination. We report the first case to our knowledge of S. dehoogii-induced subcutaneous scedosporiosis in a psoriatic patient. A 58-year-old man with 5-year history of psoriasis vulgaris and immunosuppressant therapy developed pyrexia and multiple subcutaneous abscesses on both knees. Direct microscopy of the yellowish pus showed masses of bright green short spores. Skin biopsy revealed some branched septate hyphae within the granuloma. Two aspirated pus specimens collected at a 1-week interval produced white cottony colonies on Sabouraud dextrose agar. Bacterial cultures of one blood and two purulent samples were negative, and fungal culture of blood sample was not performed. The isolate was identified as S. dehoogii using β-tubulin phylogeny and species-specific PCR with primer MSDE1/MSA2. Without addition of antifungal treatment, subcutaneous lesions disappeared spontaneously after immunosuppressant withdrawal and no relapse occurred during 64-month follow-up. The spontaneous recovery may result from immune reconstitution following immunosuppressant discontinuation.
迄今为止,仅报告过1例由德霍吉帚霉引起的创伤后眼内炎,但由于未进行病原分离和/或病理检查,不能排除其污染或定植情况。据我们所知,我们报告了首例德霍吉帚霉引起的银屑病患者皮下帚霉病病例。一名有5年寻常型银屑病病史且接受免疫抑制治疗的58岁男性,出现发热和双膝多发性皮下脓肿。对淡黄色脓液进行直接显微镜检查发现大量亮绿色短孢子。皮肤活检显示肉芽肿内有一些分支分隔菌丝。间隔1周采集的两份吸出脓液标本在沙氏葡萄糖琼脂上长出白色棉絮状菌落。一份血液样本和两份脓性样本的细菌培养均为阴性,未对血液样本进行真菌培养。使用β-微管蛋白系统发育分析和引物MSDE1/MSA2进行种特异性PCR,将分离菌株鉴定为德霍吉帚霉。未加用抗真菌治疗,停用免疫抑制剂后皮下病变自行消失,在64个月的随访期间未复发。自发恢复可能是由于停用免疫抑制剂后免疫重建所致。