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复发性多软骨炎。2例临床、病理解剖及组织化学研究。

Relapsing polychondritis. A clinical, pathologic-anatomic and histochemical study of 2 cases.

作者信息

Kindblom L G, Dalén P, Edmar G, Kjellbo H

出版信息

Acta Pathol Microbiol Scand A. 1977 Sep;85(5):656-64.

PMID:21512
Abstract

A 57-year-old man and a 70-year-old woman with relapsing polychondritis are reported. The man, suffering from arthralgias, respiratory obstruction, external ear and sanddle-nose deformities, conjunctivitis and irido-cyclitis, died after 4 years from airway obstruction because of tracheal and bronchial collapse. The woman is alive 8 months after the development of respiratory obstruction, probably caused by radiographically demonstrated tracheal obstruction, a saddle-nose deformity and hearing impairment. Microscopically, the involved cartilages showed degenerative and slight inflammatory changes and were eventually replaced by fibrous tissue. Histochemical studies, utilizing staining with Alcian blue at controlled electrolyte concentrations (Scott technique) and at controlled pH:s, with or without digestion with bacterial chondroitinase ABC; and staining with the PAS-method, with or without diastase digestion, revealed a complete or relative loss of glucosaminoglycans and glycogen. A biosynthetic defect is considered unlikely to be the primary pathogenetic mechanism of relapsing polychondritis. Histological and histochemical examination of biopsies from involved cartilages contribute to a definite diagnosis.

摘要

报告了一名57岁男性和一名70岁女性患有复发性多软骨炎。该男性患有关节痛、呼吸阻塞、外耳和鞍鼻畸形、结膜炎和虹膜睫状体炎,4年后因气管和支气管塌陷导致气道阻塞而死亡。该女性在出现呼吸阻塞8个月后仍然存活,呼吸阻塞可能是由影像学显示的气管阻塞、鞍鼻畸形和听力障碍引起的。显微镜下,受累软骨显示退行性和轻微炎症改变,最终被纤维组织取代。组织化学研究采用在可控电解质浓度(斯科特技术)和可控pH值下用阿尔辛蓝染色,有无用细菌软骨素酶ABC消化;以及用PAS法染色,有无淀粉酶消化,结果显示糖胺聚糖和糖原完全或相对缺失。生物合成缺陷不太可能是复发性多软骨炎的主要发病机制。对受累软骨活检进行组织学和组织化学检查有助于明确诊断。

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