Association of early-onset myasthenia gravis and primary Sjogren's syndrome: a case-based narrative review (August, 10.1007/s10067-022-06294-w, 2022)

被引:0
|
作者
Hartert, Marc [1 ]
Melcher, Balint [2 ]
Huertgen, Martin [1 ]
机构
[1] Kathol Klinikum Koblenz Montabaur, Dept Thorac Surg, Rudolf Virchow Str 7-9, D-56073 Koblenz, Germany
[2] Inst Pathol, Franz Weis Str 13, D-56073 Koblenz, Germany
关键词
Autoimmune disease; Coexistence; Lympho-follicular thymic hyperplasia; Myasthenia gravis; Primary Sjögren’s syndrome;
D O I
10.1007/s10067-022-06328-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Coexistent myasthenia gravis (MG) and primary Sjögren’s syndrome (pSS) is an absolute rarity. That is kind of a surprise as both entities seem to share the same corresponding immunologic mechanisms. We hereby report the case of a 41-year-old woman with coincident early-onset MG (EOMG) and pSS. Because EOMG was the leading clinical feature, she was primarily treated by innovative non-intubated uniportal subxiphoid video-assisted thoracoscopic surgery (VATS) thymectomy. As the association of EOMG and pSS is so unusual, we contextualize our findings with the relevant literature. Particular relevance is an anti-nuclear antibody screening throughout the clinical course of MG and—in reverse—a screening for MG variables when pSS patients complain either muscle fatigability or fatigable ptosis. As pSS patients do not develop any serious morbidity, supervising MG progress in patients with both diseases is of utmost importance. Apart from conscientious pSS diagnosis, prompt adjusting of EOMG progress is the essential aspect of targeted treatment. In this context, it is relevant that therapeutic decisions are made in a multidisciplinary approach. Due to its rarity, multicenter prospective studies of larger sample sizes are indispensably needed to obtain a better understanding of this unusual link. © 2022, The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).
引用
收藏
页码:3267 / 3268
页数:2
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