Primary Sjogren's syndrome with type II respiratory failure caused by myotonic dystrophy type 1: A case report and literature review

被引：1

作者：

He, Shiping ^{[1
]}

Jiang, Mengdi ^{[1
]}

Zhou, Jiaxin ^{[1
,2
]}

Jiang, Ying ^{[1
]}

Tian, Xinping ^{[1
]}

Zhang, Wen ^{[1
]}

Zeng, Xiaofeng ^{[1
]}

机构：

[1] Chinese Acad Med Sci & Peking Union Med Coll, Peking Union Med Coll Hosp, Minist Educ Key Lab, Natl Clin Res Ctr Dermatol & Immunol Dis NCRC DID,, Beijing, Peoples R China

[2] Peking Union Med Coll Hosp, Dept Rheumatol & Clin Immunol, 1 Shuai Fu Yuan, Beijing 100730, Peoples R China

来源：

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES | 2023年 / 26卷 / 05期

关键词：

dyspnea; myotonic dystrophy type 1; Sjogren's syndrome; SHRINKING LUNG;

D O I：

10.1111/1756-185X.14551

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Primary Sjogren's syndrome (pSS) is an autoimmune disease characterized by the involvement of exocrine glands with dryness of mouth and eyes as typical clinical manifestations, and may also have extra-glandular organ involvement. Myotonic dystrophy type 1 (DM1) is the most common type of adult-onset muscular dystrophy, which can lead to progressive muscle weakness and myotonia. The coexistence of pSS with DM1 was rarely reported. We here report a Chinese female pSS patient with progressive type II respiratory failure as a major manifestation and finally diagnosed with DM1 by genetic testing.

引用

页码：950 / 953

页数：4

共 18 条

[1] Relationship between chronic hypercapnia and inspiratory-muscle weakness in myotonic dystrophy [J].