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免疫功能低下儿童的铜绿假单胞菌蜂窝织炎和坏疽性脓皮病

Pseudomonas aeruginosa cellulitis and ecthyma gangrenosum in immunocompromised children.

作者信息

Fergie J E, Patrick C C, Lott L

机构信息

Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, TN 38101-0318.

出版信息

Pediatr Infect Dis J. 1991 Jul;10(7):496-500. doi: 10.1097/00006454-199107000-00003.

Abstract

Pseudomonas aeruginosa skin infections are generally considered to be secondary manifestations of disseminated disease. A retrospective analysis of all cases of P. aeruginosa skin infections seen at St. Jude Children's Research Hospital since 1962 revealed 16 episodes of the infection (ecthyma gangrenosum, 8 episodes, 7 patients; cellulitis, 8 episodes, 7 patients) in which blood cultures were uniformly negative for P. aeruginosa. All cases were identified while the patients were receiving ambulatory care. Five episodes developed while the patients' neutrophil counts were greater than 1 x 10(9) cells/liter. Eight patients had acute lymphoblastic leukemia, 2 had acute myeloid leukemia, 2 had aplastic anemia, 1 had transient agranulocytosis and 1 had cyclic neutropenia. There were no solid tumor patients. Although patients received different antibiotic combinations, all had resolutions of their lesions without fatal complications. Patients diagnosed as having cellulitis required a mean of 9.2 days of treatment with intravenous antibiotics, as compared with 17.8 days for those with ecthyma gangrenosum (P less than 0.05 by the Wilcoxon test). These observations show that P. aeruginosa skin infections can develop in the absence of bacteremia in immunocompromised children.

摘要

铜绿假单胞菌皮肤感染通常被认为是播散性疾病的继发表现。对自1962年以来在圣裘德儿童研究医院所见的所有铜绿假单胞菌皮肤感染病例进行的回顾性分析显示,有16例感染(坏疽性脓皮病8例,7名患者;蜂窝织炎8例,7名患者),其中血培养均未检出铜绿假单胞菌。所有病例均在患者接受门诊治疗时确诊。5例在患者中性粒细胞计数大于1×10⁹/升时发生。8例患者患有急性淋巴细胞白血病,2例患有急性髓细胞白血病,2例患有再生障碍性贫血,1例患有短暂性粒细胞缺乏症,1例患有周期性中性粒细胞减少症。无实体瘤患者。尽管患者接受了不同的抗生素联合治疗,但所有患者的皮损均消退,无致命并发症。诊断为蜂窝织炎的患者平均需要静脉使用抗生素治疗9.2天,而坏疽性脓皮病患者为17.8天(经威尔科克森检验,P<0.05)。这些观察结果表明,免疫功能低下的儿童在无菌血症的情况下也可发生铜绿假单胞菌皮肤感染。

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