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肺孢子丝菌病:治疗与预后综述

Pulmonary sporotrichosis: review of treatment and outcome.

作者信息

Pluss J L, Opal S M

出版信息

Medicine (Baltimore). 1986 May;65(3):143-53.

PMID:3517551
Abstract

Four culture-documented cases of pulmonary sporotrichosis, three primary infections and one with multisystem involvement, are presented. Two of these patients are the first reported cases of primary lung disease treated with ketoconazole. This antifungal agent appears to be ineffective in eradicating this infection. The four cases, as well as a review of the literature, illustrate several important aspects of this rare disease. Pulmonary sporotrichosis is most commonly found in males with a history of alcohol abuse who are between the ages of 30 and 60. The infection is usually confined to the parenchyma of the lung but can involve hilar and mediastinal lymph nodes, pleura, skin, subcutaneous tissue, and joints. All but two cases have been reported in the United States, and the majority reside within states bordering the Missouri or Mississippi rivers. Direct occupational or environmental exposure appears to be an important predisposing risk factor. The onset of the disease is insidious, presenting in a manner similar to many other granulomatous or neoplastic diseases. Tuberculosis is the most common suspected diagnosis before confirmation of sporotrichosis. The chest radiograph most commonly demonstrates upperlobe cavitary disease with surrounding parenchymal infiltrates. The diagnosis can be suspected with high serologic titers or skin-test positivity, but needs to be confirmed by culture. The organism can usually be grown from sputum, as well as routine bronchoscopic procedures, open-lung biopsy specimens or pleural fluid. Histologic examination shows granulomas of both the caseating and noncaseating varieties. Frequently, organisms can be seen in necrotic areas of the lung tissue by diastase-modified GMS or PAS staining. Staining by direct fluorescent antibody technique can also be done and appears to be highly specific. Treatment is controversial, but total surgical resection of diseased lung as well as a perioperative regimen of SSKI or amphotericin B appears to be the most efficacious therapy. Medical therapy alone with SSKI or amphotericin B may be useful in selected cases but has been disappointing in the majority of reports. The imidazoles are usually ineffective, and the search for more effective medical therapy continues.

摘要

本文报告了4例经培养确诊的肺孢子丝菌病病例,其中3例为原发性感染,1例累及多系统。这2例患者是首例报道使用酮康唑治疗原发性肺部疾病的病例。这种抗真菌药物似乎无法有效根除这种感染。这4例病例以及文献回顾阐述了这种罕见疾病的几个重要方面。肺孢子丝菌病最常见于30至60岁有酗酒史的男性。感染通常局限于肺实质,但可累及肺门和纵隔淋巴结、胸膜、皮肤、皮下组织及关节。除2例病例外,其余均在美国报道,大多数病例位于密苏里河或密西西比河沿岸各州。直接的职业或环境暴露似乎是一个重要的易感危险因素。该病起病隐匿,表现方式与许多其他肉芽肿性或肿瘤性疾病相似。在确诊孢子丝菌病之前,最常见的疑似诊断是肺结核。胸部X线片最常见的表现是上叶空洞性病变伴周围实质浸润。高血清学滴度或皮肤试验阳性可怀疑该病,但需要通过培养确诊。该病原体通常可从痰液、常规支气管镜检查标本、开胸肺活检标本或胸腔积液中培养出来。组织学检查显示有干酪样和非干酪样肉芽肿。通过淀粉酶改良的GMS或PAS染色,通常可在肺组织坏死区域见到病原体。也可采用直接荧光抗体技术染色,且似乎具有高度特异性。治疗存在争议,但对患病肺组织进行全肺切除以及围手术期使用SSKI或两性霉素B似乎是最有效的治疗方法。单独使用SSKI或两性霉素B进行药物治疗在某些病例中可能有用,但在大多数报告中效果不佳。咪唑类药物通常无效,对更有效药物治疗的探索仍在继续。

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