Haight D O, Esperanza L E, Greene J N, Sandin R L, DeGregorio R, Spiers A S
Department of Medicine, University of South Florida College of Medicine, Tampa.
Am J Med Sci. 1994 Sep;308(3):192-5. doi: 10.1097/00000441-199409000-00015.
Cutaneous cryptococcosis usually is associated with concurrent systemic infection and actually may develop before clinical manifestations of cryptococcal meningitis become apparent. It is rare for a cryptococcal infection to be localized only to the skin. A case of cutaneous cryptococcosis is described in an immunocompromised patient who initially had a rash and a positive serum cryptococcal antigen titer, but no central nervous system involvement. The papular pustular skin lesions disappeared after 8 weeks of therapy with amphotericin B, which was stopped secondary to progressive azotemia. Less than 2 months after therapy, the skin lesions recurred, again without evidence of systemic disease. Treatment with oral fluconazole resulted in a gradual resolution of the cutaneous lesions. The pathogenesis of cryptococcosis is discussed, with emphasis on the management of cutaneous cryptococcosis.
皮肤隐球菌病通常与并发的全身感染相关,实际上可能在隐球菌性脑膜炎的临床表现出现之前就已发生。隐球菌感染仅局限于皮肤的情况较为罕见。本文描述了一例免疫功能低下患者的皮肤隐球菌病,该患者最初出现皮疹且血清隐球菌抗原滴度呈阳性,但无中枢神经系统受累。在用两性霉素B治疗8周后,丘疹脓疱性皮肤病变消失,因进行性氮质血症而停药。治疗后不到2个月,皮肤病变复发,同样没有全身疾病的证据。口服氟康唑治疗使皮肤病变逐渐消退。本文讨论了隐球菌病的发病机制,重点是皮肤隐球菌病的管理。