Xiujiao Xia, Ai'e Xu
Department of Dermatology, 3rd Hospital, Hangzhou, China.
Mycoses. 2005 Jul;48(4):238-41. doi: 10.1111/j.1439-0507.2005.01079.x.
We report two cases of cutaneous cryptococcosis in male patients without underlying disease. Case 1 had a granulomatous mass on his right neck, gradually enlarging for 3 months. After the mass was debrided surgically in a hospital, the incision wound gradually developed into a severe ulceration. Mycological examination revealed Cryptococcus neoformans infection. It was significant that histopathology of both pre-surgery granuloma and post-surgery ulceration revealed thick-walled spores with thick capsule. Chest X-ray revealed a shadow in the left lower lung. After treatment with amphotec for 21 days, the lesion healed. Case 2 had an approximately 2 x 2 cm solitary dull nodule on his right thigh, which had been present for 8 months. Mycological examination confirmed that the lesion was caused by C. neoformans. The patient's ratio of peripheral blood CD4(+) cell was slightly reduced. After 14 days of treatment with oral fluconazole, followed by oral itraconazole for 2 months, mycological and clinical cure were achieved. The two isolates were identified as C. neoformans var. gattii serotype C and C. neoformans var. grubii serotype A.
我们报告两例无基础疾病男性患者的皮肤隐球菌病。病例1右侧颈部有一肉芽肿性肿块,逐渐增大3个月。在医院对肿块进行手术清创后,切口伤口逐渐发展为严重溃疡。真菌学检查显示新型隐球菌感染。值得注意的是,术前肉芽肿和术后溃疡的组织病理学检查均显示有厚壁孢子且有厚荚膜。胸部X线显示左下肺有阴影。用两性霉素B治疗21天后,病变愈合。病例2右侧大腿有一个约2×2 cm的孤立性暗红色结节,已存在8个月。真菌学检查证实该病变由新型隐球菌引起。患者外周血CD4(+)细胞比例略有降低。口服氟康唑治疗14天,随后口服伊曲康唑2个月后,实现了真菌学和临床治愈。这两个分离株分别鉴定为新生隐球菌变种格特隐球菌血清型C和新生隐球菌变种格鲁比隐球菌血清型A。