Bonduel M, Santos P, Turienzo C F, Chantada G, Paganini H
Department of Hematology/Oncology, Hospital de Pediatría Prof Dr Juan P Garrahan, Buenos Aires, Argentina.
Bone Marrow Transplant. 2001 Jun;27(12):1311-3. doi: 10.1038/sj.bmt.1703072.
We report two patients who developed atypical skin lesions caused by Curvularia sp. and Pseudallescheria boydii after allogeneic bone marrow transplantation for severe aplastic anemia. The first patient (female, 18-year-old) had multiple hemorrhagic vesicles on day +30 after her second BMT for graft failure. Pseudallescheria boydii was isolated from a skin biopsy. The patient died of respiratory failure probably as a consequence of systemic fungal infection. The second patient (male, 9-year-old) developed an ecthyma gangrenosum-like lesion on his right palm on day +8. Curvularia sp. was isolated from a skin biopsy. Liposomal amphotericin was given to achieve a total dose of 30 mg/kg and followed by oral itraconazole until steroids were discontinued. The infection resolved completely and the patient has remained disease-free. We conclude that emerging fungal organisms such as those described in this report are increasingly recognized in this setting. Early recognition and biopsy of these cutaneous lesions will allow prompt initiation of therapy to prevent systemic infection.
我们报告了两名在接受异基因骨髓移植治疗严重再生障碍性贫血后出现由弯孢霉属和波氏假阿利什菌引起的非典型皮肤病变的患者。首例患者(女性,18岁)在第二次骨髓移植后第30天因移植失败出现多处出血性水疱。从皮肤活检中分离出波氏假阿利什菌。患者死于呼吸衰竭,可能是系统性真菌感染的结果。第二例患者(男性,9岁)在第8天右手掌出现坏疽性脓皮病样病变。从皮肤活检中分离出弯孢霉属。给予脂质体两性霉素,使总剂量达到30mg/kg,随后口服伊曲康唑,直至停用类固醇。感染完全消退,患者至今无病生存。我们得出结论,如本报告中所述的新兴真菌病原体在这种情况下越来越受到认可。对这些皮肤病变进行早期识别和活检将有助于及时开始治疗,以预防系统性感染。