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脂膜炎:痛风的另一种临床表现。

Panniculitis: another clinical expression of gout.

机构信息

Rheumatology Unit, National University School of Medicine, Bogota, Colombia.

出版信息

Rheumatol Int. 2011 Jun;31(6):831-5. doi: 10.1007/s00296-010-1561-8. Epub 2010 Aug 21.

Abstract

Gouty panniculitis is an unusual clinical manifestation of gout, characterized by the deposition of monosodium urate crystals in the lobular hypodermis. Its pathogenesis is poorly understood but is associated with hyperuricemia, and the clinical presence of indurate subcutaneous plaques, which may precede or appear subsequently to the articular clinical expression of tophaceous gout. The aim of this report is to describe the clinical characteristics and potential risk factors for the development of lobular panniculitis secondary to chronic tophaceous gout. This is a retrospective clinical review of 6 patients with gouty panniculitis seen at the rheumatology service at the National University of Colombia. All cases fulfill diagnostic criteria for gout. The presenting clinical characteristics of each case were analyzed. All 6 patients were men, with an average age of 26 years. Two patients initially presented with cutaneous manifestations, and in the remainder 4 joint involvements preceded the cutaneous manifestations. Articular involvement first developed in lower extremities, of intermittent nature, and subsequent occurrence of polyarthritis of upper and lower extremities. A positive family history of gout was observed in half of the patients. Smoking and high alcohol intake were relevant risk factors. On physical examination, all exhibited the presence of erythematous, irregular surface, deep indurate subcutaneous plaques. Biopsy of skin and deep dermis including panniculus revealed the presence of granulomatous inflammatory changes with deposition of amorphous eosinophilic material surrounded by palisading histocytes and lymphocytes. Characteristic negative birefringent monosodium urate crystals were observed in the synovial fluid of patients with arthritis. All patients exhibited high levels of serum uric acid and were non-complaint to treatment with allopurinol, NSAIDs, and colchicine. Gouty panniculitis should be considered in the differential diagnosis of panniculitis, especially in the presence of high levels of uric acid. It is usually observed in the third decade of life and may appear prior to the inflammatory articular manifestations of tophaceous gout.

摘要

痛风性脂膜炎是一种不常见的痛风临床表现,其特征是单钠尿酸盐晶体在小叶真皮下沉积。其发病机制尚不清楚,但与高尿酸血症有关,临床表现为硬结性皮下斑块,可先于或后于痛风石性痛风的关节临床表现出现。本报告的目的是描述继发于慢性痛风石性痛风的小叶性脂膜炎的临床特征和潜在的发病危险因素。这是对在哥伦比亚国立大学风湿病科就诊的 6 例痛风性脂膜炎患者进行的回顾性临床研究。所有病例均符合痛风的诊断标准。分析了每个病例的临床表现特征。6 例患者均为男性,平均年龄 26 岁。2 例患者最初表现为皮肤表现,其余 4 例关节受累先于皮肤表现。关节受累首先发生在下肢,呈间歇性,随后出现上肢和下肢多发性关节炎。一半的患者有痛风家族史。吸烟和大量饮酒是相关的危险因素。体格检查时,所有患者均出现红斑、不规则表面、深硬结性皮下斑块。皮肤和深真皮活检包括脂膜炎,显示存在肉芽肿性炎症改变,有不定形嗜酸性物质沉积,周围有栅栏状组织细胞和淋巴细胞。关节炎患者的关节液中观察到特征性的负双折射单钠尿酸盐晶体。所有患者均表现为血尿酸水平升高,且对别嘌醇、非甾体抗炎药和秋水仙碱的治疗不依从。在鉴别诊断脂膜炎时,应考虑痛风性脂膜炎,特别是在尿酸水平升高的情况下。它通常发生在 30 多岁,可能先于痛风石性痛风的炎症性关节表现出现。

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