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获得性免疫缺陷综合征的胸部表现

Thoracic manifestations of the acquired immune deficiency syndrome.

作者信息

Pass H I, Potter D A, Macher A M, Reichert C, Shelhammer J H, Masur H, Ognibene F, Gelmann E, Lane H C, Fauci A

出版信息

J Thorac Cardiovasc Surg. 1984 Nov;88(5 Pt 1):654-8.

PMID:6333556
Abstract

The acquired immune deficiency syndrome is characterized by the development of multiple recurrent opportunistic infections or unusual neoplasms in individuals with no prior history of immune suppression. This report summarizes the thoracic diseases encountered in such patients before after death and the role of diagnostic techniques currently used in the evaluation of thoracic disease in 15 patients with this syndrome. Efficacy of treatment was determined by correlation with postmortem findings in all patients. Pulmonary disease was present in all 15 patients and necessitated 23 transbronchial biopsies in 11 patients. Pneumocystis carinii pneumonia and cytomegalovirus pneumonia were the most common findings. Nine open lung biopsies in eight patients disclosed either Pneumocystis carinii pneumonia or Kaposi's sarcoma. Esophageal disease was present in four patients, and endoscopic evaluation demonstrated Candida esophagitis (two), esophageal Kaposi's sarcoma (one), and cytomegalovirus esophagitis and Kaposi's sarcoma (one). Mean time to death from diagnosis of acquired immune deficiency syndrome was 7.7 months, with respiratory insufficiency being the most common cause of death (9/15, 60%). Pneumocystis carinii pneumonia was successfully eradicated in 70% of the patients. Candida esophagitis was ameliorated in both patients with the disease. Unsuspected pulmonary Kaposi's sarcoma, cytomegalovirus pneumonitis, and other infectious pathogens were documented at autopsy. These data reveal that Pneumocystis carinii pneumonia and Candida esophagitis can be managed successfully in patients with acquired immune deficiency syndrome if appropriately diagnosed. The major cause of death in this series was pulmonary insufficiency, often the result of severe cytomegalovirus infection. Thoracic surgeons must continue to play an aggressive and important role in the early diagnosis and management of potentially treatable pulmonary and esophageal disease in these patients.

摘要

获得性免疫缺陷综合征的特征是在既往无免疫抑制病史的个体中发生多种复发性机会性感染或罕见肿瘤。本报告总结了15例该综合征患者生前和死后所遇到的胸部疾病,以及目前用于评估胸部疾病的诊断技术所起的作用。通过与所有患者的尸检结果相关联来确定治疗效果。15例患者均有肺部疾病,11例患者需要进行23次经支气管活检。卡氏肺孢子虫肺炎和巨细胞病毒肺炎是最常见的发现。8例患者进行了9次开胸肺活检,结果显示为卡氏肺孢子虫肺炎或卡波西肉瘤。4例患者有食管疾病,内镜检查显示念珠菌食管炎(2例)、食管卡波西肉瘤(1例)、巨细胞病毒食管炎和卡波西肉瘤(1例)。从获得性免疫缺陷综合征诊断到死亡的平均时间为7.7个月,呼吸功能不全是最常见的死亡原因(9/15,60%)。70%的患者卡氏肺孢子虫肺炎得到成功根除。2例念珠菌食管炎患者的病情均有所改善。尸检发现了未被怀疑的肺部卡波西肉瘤、巨细胞病毒性肺炎和其他感染性病原体。这些数据表明,如果得到适当诊断,获得性免疫缺陷综合征患者的卡氏肺孢子虫肺炎和念珠菌食管炎可以得到成功治疗。本系列中主要的死亡原因是肺功能不全,通常是严重巨细胞病毒感染的结果。胸外科医生必须在这些患者潜在可治疗的肺部和食管疾病的早期诊断和治疗中继续发挥积极且重要的作用。

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