Mays Steven R, Bogle Melissa A, Bodey Gerald P
Department of Dermatology, University of Texas Medical School, Houston, Texas 77030, USA.
Am J Clin Dermatol. 2006;7(1):31-43. doi: 10.2165/00128071-200607010-00004.
There are two main types of fungal infections in the oncology patient: primary cutaneous fungal infections and cutaneous manifestations of fungemia. The main risk factor for all types of fungal infections in the oncology patient is prolonged and severe neutropenia; this is especially true for disseminated fungal infections. Severe neutropenia occurs most often in leukemia and lymphoma patients exposed to high-dose chemotherapy. Fungal infections in cancer patients can be further divided into five groups: (i) superficial dermatophyte infections with little potential for dissemination; (ii) superficial candidiasis; (iii) opportunistic fungal skin infections with distinct potential for dissemination; (iv) fungal sinusitis with cutaneous extension; and (v) cutaneous manifestations of disseminated fungal infections. In the oncology population, dermatophyte infections (i) and superficial candidiasis (ii) have similar presentations to those seen in the immunocompetent host. Primary cutaneous mold infections (iii) are especially caused by Aspergillus, Fusarium, Mucor, and Rhizopus spp. These infections may invade deeper tissues and cause disseminated fungal infections in the neutropenic host. Primary cutaneous mold infections are treated with systemic antifungal therapy and sometimes with debridement. The role of debridement in the severely neutropenic patient is unclear. In some patients with an invasive fungal sinusitis (iv) there may be direct extension to the overlying skin, causing a fungal cellulitis of the face. Aspergillus, Rhizopus, and Mucor spp. are the most common causes. We also describe the cutaneous manifestations of disseminated fungal infections (v). These infections usually occur in the setting of prolonged neutropenia. The most common causes are Candida, Aspergillus, and Fusarium spp. Therapy is with systemic antifungal therapy. The relative efficacies of amphotericin B, fluconazole, itraconazole, voriconazole, and caspofungin are discussed. Recovery from disseminated fungal infections is unlikely, however, unless the patient's neutropenia resolves.
原发性皮肤真菌感染和真菌血症的皮肤表现。肿瘤患者发生各类真菌感染的主要危险因素是长期严重的中性粒细胞减少;对于播散性真菌感染尤其如此。严重中性粒细胞减少最常发生在接受大剂量化疗的白血病和淋巴瘤患者中。癌症患者的真菌感染可进一步分为五组:(i)几乎没有播散可能的浅表皮肤癣菌感染;(ii)浅表念珠菌病;(iii)有明显播散可能的机会性真菌皮肤感染;(iv)伴有皮肤蔓延的真菌性鼻窦炎;(v)播散性真菌感染的皮肤表现。在肿瘤人群中,皮肤癣菌感染(i)和浅表念珠菌病(ii)的表现与免疫功能正常宿主中的表现相似。原发性皮肤霉菌感染(iii)尤其由曲霉属、镰刀菌属、毛霉属和根霉属等引起。这些感染可能侵入更深层组织,并在中性粒细胞减少的宿主中导致播散性真菌感染。原发性皮肤霉菌感染采用全身性抗真菌治疗,有时还需清创。清创在严重中性粒细胞减少患者中的作用尚不清楚。在一些侵袭性真菌性鼻窦炎(iv)患者中,可能直接蔓延至上方皮肤,导致面部真菌性蜂窝织炎。曲霉属、根霉属和毛霉属是最常见的病因。我们还描述了播散性真菌感染的皮肤表现(v)。这些感染通常发生在长期中性粒细胞减少的情况下。最常见的病因是念珠菌属、曲霉属和镰刀菌属。治疗采用全身性抗真菌治疗。文中讨论了两性霉素B、氟康唑、伊曲康唑、伏立康唑和卡泊芬净的相对疗效。然而,除非患者的中性粒细胞减少症得到缓解,否则播散性真菌感染不太可能痊愈。