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[韦格纳肉芽肿病的耳鼻喉科诊断]

[ENT diagnosis of Wegener's syndrome].

作者信息

López Amado M, Arrojo Alonso F, García Sarandeses A, Herranz González J, Martínez Vidal J

机构信息

Servicio de Otorrinolaringología, Hospital Juan Canalejo, La Coruña.

出版信息

An Otorrinolaringol Ibero Am. 1994;21(4):343-55.

PMID:8092442
Abstract

In spite of its rarity Wegener's granulomatosis is of great concern to be otolaryngologist because the malady may start in the territory of the speciality, challenging the actual diagnosis, owing to the inespecificity of the symptomatology, to its torpid evolution, as well as the potential harmfullness of process. This paper inform of the retrospective study done by the AA. in the last ten years, about 4 cases diagnosed and treated by them. All the possible diagnostic measures are contemplated: clinical and histopathological findings and the newly introduced tests for anticytoplasmatic antibodies against the neutrophiles. A review of the bibliography on the subject is adjoined. All the considered patients consulted at the beginning with the otolaryngologist. Diagnostic suspicion aroused only in patients with nasal complaints (50 percent) and were not under suspicion those with ear symptoms. Positive diagnosis were confirmed in all cases through renal biopsies. Nasal biopsies resulted negatives. When the syndrome started in low aged patients the evolutive course showed deleterious and the affected died after a short term of few months. In more aged a survival of 8-9 yeas was reached.

摘要

尽管韦格纳肉芽肿病罕见,但它引起了耳鼻喉科医生的极大关注,因为这种疾病可能始于该专业领域,由于症状不具特异性、病情发展缓慢以及该疾病过程的潜在危害性,对实际诊断构成挑战。本文介绍了作者在过去十年中对4例经其诊断和治疗的病例进行的回顾性研究。考虑了所有可能的诊断措施:临床和组织病理学发现以及新引入的抗中性粒细胞胞浆抗体检测。并附有该主题的文献综述。所有被考虑的患者最初都咨询了耳鼻喉科医生。仅在有鼻部症状的患者中引起诊断怀疑(50%),而有耳部症状的患者未被怀疑。所有病例均通过肾活检确诊。鼻活检结果为阴性。当该综合征在低龄患者中开始时,病情发展显示有害,患者在短短几个月内死亡。在年龄较大的患者中,存活期可达8至9年。

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