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A 5-Year Follow-Up of Triple-Seronegative Myasthenia Gravis Successfully Treated with Tacrolimus Therapy.

Authors :
Takenori Tozawa
Nishimura, Akira
Tamaki Ueno
Daisuke Kaneda
Yuri Miyanomae
Tomohiro Chiyonobu
Masafumi Morimoto
Hajime Hosoi
Source :
Neuropediatrics; 2018, Vol. 49 Issue 3, p200-203, 4p
Publication Year :
2018

Abstract

Seronegativemyasthenia gravis (MG) is a generalized formof MG that is diagnosed on the basis of clinical symptoms, electrophysiological testing, and pharmacological responses, in the absence of a seropositive status for anti-acetylcholine receptor (AChR) antibodies. Generalized MGthat is seronegative for anti-AChR, anti-muscle-specific kinase (MuSK), and anti-low density lipoprotein receptor related protein 4 (Lrp4) antibodies is known as tripleseronegative MG. We here describe a case of triple-seronegative MG in an 8-year-old boy. His first symptom was dysphagia, at 3 years of age, and he subsequently developed ptosis, rhinolalia, and a waddling gait. A genetic analysis was conducted to exclude the possibility of congenital myasthenia syndrome due to the patient's resistance to steroid therapy. His conditionwas successfullymanaged with tacrolimus therapy over a 5-year follow-up period. Recently, several studies have reported the therapeutic utility of tacrolimus in juvenile seropositiveMG; in contrast, a fewreports have described tacrolimus treatment in cases of seronegativeMG.Our findings suggest that tacrolimus therapy is a safeand effective option for the treatment of juvenile seronegative MG. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
0174304X
Volume :
49
Issue :
3
Database :
Complementary Index
Journal :
Neuropediatrics
Publication Type :
Academic Journal
Accession number :
129558285
Full Text :
https://doi.org/10.1055/s-0037-1618591