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人类免疫缺陷病毒感染患者的杆菌性血管瘤病和杆菌性紫癜:一项病例对照研究中的临床特征

Bacillary angiomatosis and bacillary peliosis in patients infected with human immunodeficiency virus: clinical characteristics in a case-control study.

作者信息

Mohle-Boetani J C, Koehler J E, Berger T G, LeBoit P E, Kemper C A, Reingold A L, Plikaytis B D, Wenger J D, Tappero J W

机构信息

Childhood and Respiratory Disease Branch, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

Clin Infect Dis. 1996 May;22(5):794-800. doi: 10.1093/clinids/22.5.794.

Abstract

Clinical characteristics associated with bacillary angiomatosis and bacillary peliosis (BAP) in patients with human immunodeficiency virus (HIV) infection were evaluated in a case-control study; 42 case-patients and 84 controls were matched by clinical care institution. Case-patients presented with fever (temperature, > 37.8 degrees C; 93%), a median CD4 lymphocyte count of 21/mm3, cutaneous or subcutaneous vascular lesions (55%), lymphadenopathy (21%), and/or abdominal symptoms (24%). Many case-patients experienced long delays between medical evaluation and diagnosis of BAP (median, 4 weeks; range, 1 day to 24 months). Case-patients were more likely than controls to have fever, lymphadenopathy, hepatomegaly, splenomegaly, a low CD4 lymphocyte count, anemia, or an elevated serum level of alkaline phosphatase (AP) (P < .001). In multivariate analysis, a CD4 lymphocyte count of < 200/mm3 (matched odds ratio [OR], 9.9; P < .09), anemia reflected by a hematocrit value of < 0.36 (OR, 19.7; P < .04), and an elevated AP level of > or = 2.6 mukat/L (OR, 23.9; P < .05) remained associated with disease after therapy with zidovudine was controlled for. BAP should be considered an AIDS-defining opportunistic infection and should be included in the differential diagnosis for febrile, HIV-infected patients with cutaneous or osteolytic lesions, lymphadenopathy, abdominal symptoms, anemia, or an elevated serum level of AP.

摘要

在一项病例对照研究中,对人类免疫缺陷病毒(HIV)感染患者中与杆菌性血管瘤病和杆菌性紫癜(BAP)相关的临床特征进行了评估;42例病例患者和84例对照者按临床护理机构进行匹配。病例患者出现发热(体温>37.8℃;93%),CD4淋巴细胞计数中位数为21/mm³,皮肤或皮下血管病变(55%),淋巴结病(21%),和/或腹部症状(24%)。许多病例患者在BAP的医学评估和诊断之间经历了长时间的延迟(中位数为4周;范围为1天至24个月)。病例患者比对照者更有可能出现发热、淋巴结病、肝肿大、脾肿大、CD4淋巴细胞计数低、贫血或血清碱性磷酸酶(AP)水平升高(P<.001)。在多变量分析中,在控制齐多夫定治疗后,CD4淋巴细胞计数<200/mm³(匹配优势比[OR]为9.9;P<.09)、血细胞比容值<0.36反映的贫血(OR为19.7;P<.04)以及AP水平升高≥2.6mukat/L(OR为23.9;P<.05)仍与疾病相关。BAP应被视为一种艾滋病定义的机会性感染,应纳入对有发热、皮肤或溶骨性病变、淋巴结病、腹部症状、贫血或血清AP水平升高的HIV感染患者的鉴别诊断中。

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