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德克萨斯州的利什曼病:人类病例的流行病学和临床特征

Leishmaniasis in Texas: epidemiology and clinical aspects of human cases.

作者信息

McHugh C P, Melby P C, LaFon S G

机构信息

Occupational and Environmental Health Directorate, Armstrong Laboratory, Brooks Air Force Base, Texas, USA.

出版信息

Am J Trop Med Hyg. 1996 Nov;55(5):547-55. doi: 10.4269/ajtmh.1996.55.547.

Abstract

Twenty-seven autochthonous cases of cutaneous leishmaniasis in Texas were identified by contact with dermatologists and State Health Department officials, and by a review of medical records, pathology reports, and previously published case reports. Fifteen cases were previously unreported. Although the date of onset of the first recognized case was 1903, in 20 of the cases the date of onset of the lesion(s) was in 1980-1989. Twelve cases were female; 15 were male. Age at diagnosis ranged from two to 86 (median 37) years. The disease was identified significantly more frequently in younger males and older females. The distribution of cases closely followed the distribution of Neotoma micropus, a rodent host for Leishmania mexicana. The most common risk factor appeared to be residence or activity in close proximity to woodrat habitat. Two cases lived in central Texas; the remainder had a residence in, or history of travel to, southern Texas. A majority of cases were first recognized during the cooler months of the year. Most lesions began as papules or nodules that subsequently ulcerated. In 20 cases, a single lesion was present. Five cases had resolution of their lesions without receiving specific anti-leishmanial therapy; lesions of 17 resolved after treatment with a variety of therapies. One life-long case of disseminated disease failed to respond to treatment, and four cases were lost to follow-up. A Leishmania-specific lymphocyte proliferation assay gave a positive response for four of five cases tested. Screening of 13 family members found no evidence of subclinical infection. These 27 cases, and two recently recognized cases reported in a note added in proof, indicate that cutaneous leishmaniasis may be more common in Texas than previously thought.

摘要

通过与皮肤科医生和州卫生部门官员联系,并查阅病历、病理报告及先前发表的病例报告,在得克萨斯州确认了27例皮肤利什曼病本土病例。其中15例此前未报告过。尽管首例确诊病例的发病时间为1903年,但20例病例的皮损发病时间在1980 - 1989年。12例为女性,15例为男性。诊断时的年龄范围为2岁至86岁(中位数37岁)。该病在年轻男性和老年女性中确诊的频率明显更高。病例分布与墨西哥利什曼原虫的啮齿动物宿主小囊鼠的分布密切相关。最常见的危险因素似乎是居住在靠近林鼠栖息地的地方或在其附近活动。2例居住在得克萨斯州中部;其余病例居住在得克萨斯州南部或有前往该地区的旅行史。大多数病例在一年中较凉爽的月份首次被确认。大多数皮损最初为丘疹或结节,随后溃疡。20例有单个皮损。5例未经特异性抗利什曼治疗皮损即消退;17例经多种治疗后皮损消退。1例播散性疾病的终身病例治疗无效,4例失访。利什曼原虫特异性淋巴细胞增殖试验对5例检测病例中的4例呈阳性反应。对13名家庭成员进行筛查未发现亚临床感染的证据。这27例病例,以及在一篇校样增注中报告的2例最近确诊的病例,表明皮肤利什曼病在得克萨斯州可能比以前认为的更为常见。

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