肺泡微石症与类风湿关节炎:1例报告及文献复习。

Case Reports in Rheumatology Pub Date : 2021-05-31 eCollection Date: 2021-01-01 DOI:10.1155/2021/8811507
Waleed Hafiz, Ahmedhusam Alahmed, Mohammed Alahmadi, Rakan Alotaibi, Abdullah Alsharif, Safwan Alim, Mohammed Mokhtar, Kholoud Al-Maabdi, Omaima Badr
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引用次数: 1

摘要

肺泡微石症是一种罕见的常染色体隐性遗传病,其特征是肺泡内形成过多的磷酸钙微石。由于病情进展缓慢,大多数患者在成年时被诊断出来。儿童无症状,肺实质的改变通常是偶然发现的。诊断是由积极的胸部影像学和组织学检查相结合。类风湿性关节炎(RA)是一种慢性全身性自身免疫性疾病,以慢性血清阳性对称炎性多关节炎为特征,伴有许多关节外表现。它的目标是滑膜的衬里,通常对女性的影响大于男性,并且用抗风湿药物(DMARDs)治疗。如果不及时治疗,它会导致发病率、死亡率和社会经济负担增加。在这个病例中,我们报告了一位19岁的年轻人,他表现出与RA相关的PAM的临床和影像学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Pulmonary Alveolar Microlithiasis and Rheumatoid Arthritis: A Case Report and Review of the Literature.

Pulmonary Alveolar Microlithiasis and Rheumatoid Arthritis: A Case Report and Review of the Literature.

Pulmonary Alveolar Microlithiasis and Rheumatoid Arthritis: A Case Report and Review of the Literature.

Pulmonary alveolar microlithiasis is a rare autosomal recessive condition that is characterized by the formation of excessive calcium phosphate microliths in the alveoli. Most patients are diagnosed in adulthood due to the slow progression of the disease. Children with this disease are asymptomatic, and changes in the lung parenchyma are usually discovered incidentally. The diagnosis is made by the combination of a positive chest imaging and histological examination. Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease characterized by chronic seropositive symmetrical inflammatory polyarthritis with numerous extra-articular manifestations. It targets the lining of the synovial membranes, frequently affects females more than males, and is treated with the disease-modifying antirheumatic drugs (DMARDs). If left untreated, it leads to increased morbidity, mortality, and socioeconomic burdens. In this case, we report a 19-year-old young man who presented with clinical and radiographic features of PAM associated with RA.

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