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

L. Kindblom, P. Dalén, G. Edmar, H. Kjellbo
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引用次数: 10

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.
复发polychondritis。2例临床、病理解剖及组织化学分析。
我们报告了一名57岁男性和一名70岁女性的复发性多软骨炎。该男子患有关节痛、呼吸阻塞、外耳和鼻梁畸形、结膜炎和虹膜环炎,4年后因气管和支气管塌陷而死于气道阻塞。该妇女在出现呼吸阻塞8个月后存活,可能是由x线摄影证实的气管阻塞、鞍鼻畸形和听力障碍引起的。显微镜下,受累的软骨表现为退行性和轻微的炎症改变,最终被纤维组织所取代。组织化学研究,在控制电解质浓度(Scott技术)和控制pH:s下,用阿利新蓝染色,用细菌软骨素酶ABC消化或不消化;用pas法染色,有或没有淀粉酶消化,显示葡萄糖氨基聚糖和糖原完全或相对损失。生物合成缺陷被认为不太可能是复发性多软骨炎的主要发病机制。受累软骨的组织学和组织化学检查有助于明确的诊断。
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