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Yıl 2025, Cilt: 25 Sayı: 3, 172 - 175, 31.10.2025
https://doi.org/10.26650/jchild.2025.1704940

Öz

Kaynakça

  • Gilhus NE, Verschuuren JJ. MYasthenia gravis: subgroup classification and therapeutic strategies. Lancet Neurol. 2015;14:1023-36. google scholar
  • Deymeer F. MYasthenia gravis: MuSK MG, late-onset MG and ocular MG. Acta MYol. 2020;39:345-52. google scholar
  • Tannemaat MR, Huijbers MG, Verschuuren JJGM. MYasthenia gravis-Pathophysiology, diagnosis, and treatment. Handb Clin Neurol. 2024;200:283-305. google scholar
  • Vesperinas-Castro A, Cortes-Vicente E. Rituximab treatment in mYasthenia gravis. Front Neurol. 2023;14:1275533. google scholar
  • Rodolico C, Bonanno C, Toscano A, Vita G. MuSK-Associated MYasthenia Gravis: Clinical Features and Management. Front Neurol. 2020;11:660. google scholar
  • Evoli A, Alboini PE, Damato V, et al. MYasthenia gravis with antibodies to MuSK: an update. Ann N Y Acad Sci. 2018;1412:82-9. google scholar
  • Sanders DB, El-Salem K, MasseY JM, McConville J, Vincent A. Clinical aspects of MuSK antibody positive seronegative MG. NeurologY. 2003;60:1978-80. google scholar
  • Huda S, Waters P, Woodhall M, et al. IgG-specific cell-based assaY detects potentiallY pathogenic MuSK-Abs in seronegative MG. Neurol Neuroimmunol Neuroinflamm. 2017;4:357. google scholar
  • Anlar B, Yilmaz V, Saruhan-Direskeneli G. Long remission in muscle-specific kinase antibody-positive juvenile mYasthenia. Pediatr Neurol. 2009;40:455-6. google scholar
  • Hehir MK, Hobson-Webb LD, Benatar M, et al. Rituximab as treatment for anti-MuSK mYasthenia gravis: Multicenter blinded prospective review. NeurologY. 2017;89:1069-77. google scholar
  • Topakian R, Zimprich F, Iglseder S, et al. High efficacY of rituximab for mYasthenia gravis: a comprehensive nationwide studY in Austria. J Neurol. 2019;266:699-06. google scholar
  • O'Connell K, Ramdas S, Palace J. Management of Juvenile MYasthenia Gravis. Front Neurol. 2020;11:743. google scholar

Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab

Yıl 2025, Cilt: 25 Sayı: 3, 172 - 175, 31.10.2025
https://doi.org/10.26650/jchild.2025.1704940

Öz

Muscle-specific tyrosine kinase antibody-associated myasthenia gravis (MuSK-MG) is a rare subtype of MG distinguished by recurring relapses and a clinical history unresponsive to conventional therapies. Rituximab, a monoclonal antibody that targets CD20+ B cells, has effectively induced long-term remission in adults. We report a pediatric MuSK-MG patient who exhibited a favourable response to rituximab following the ineffectiveness of steroid therapy and acetylcholinesterase inhibitor (AChEI) therapy.

Kaynakça

  • Gilhus NE, Verschuuren JJ. MYasthenia gravis: subgroup classification and therapeutic strategies. Lancet Neurol. 2015;14:1023-36. google scholar
  • Deymeer F. MYasthenia gravis: MuSK MG, late-onset MG and ocular MG. Acta MYol. 2020;39:345-52. google scholar
  • Tannemaat MR, Huijbers MG, Verschuuren JJGM. MYasthenia gravis-Pathophysiology, diagnosis, and treatment. Handb Clin Neurol. 2024;200:283-305. google scholar
  • Vesperinas-Castro A, Cortes-Vicente E. Rituximab treatment in mYasthenia gravis. Front Neurol. 2023;14:1275533. google scholar
  • Rodolico C, Bonanno C, Toscano A, Vita G. MuSK-Associated MYasthenia Gravis: Clinical Features and Management. Front Neurol. 2020;11:660. google scholar
  • Evoli A, Alboini PE, Damato V, et al. MYasthenia gravis with antibodies to MuSK: an update. Ann N Y Acad Sci. 2018;1412:82-9. google scholar
  • Sanders DB, El-Salem K, MasseY JM, McConville J, Vincent A. Clinical aspects of MuSK antibody positive seronegative MG. NeurologY. 2003;60:1978-80. google scholar
  • Huda S, Waters P, Woodhall M, et al. IgG-specific cell-based assaY detects potentiallY pathogenic MuSK-Abs in seronegative MG. Neurol Neuroimmunol Neuroinflamm. 2017;4:357. google scholar
  • Anlar B, Yilmaz V, Saruhan-Direskeneli G. Long remission in muscle-specific kinase antibody-positive juvenile mYasthenia. Pediatr Neurol. 2009;40:455-6. google scholar
  • Hehir MK, Hobson-Webb LD, Benatar M, et al. Rituximab as treatment for anti-MuSK mYasthenia gravis: Multicenter blinded prospective review. NeurologY. 2017;89:1069-77. google scholar
  • Topakian R, Zimprich F, Iglseder S, et al. High efficacY of rituximab for mYasthenia gravis: a comprehensive nationwide studY in Austria. J Neurol. 2019;266:699-06. google scholar
  • O'Connell K, Ramdas S, Palace J. Management of Juvenile MYasthenia Gravis. Front Neurol. 2020;11:743. google scholar
Toplam 12 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Çocuk Sağlığı ve Hastalıkları (Diğer)
Bölüm Olgu Sunumu
Yazarlar

Arife Derda Yücel Şen 0000-0002-2656-5611

Ahmet Baysal 0000-0002-5909-1918

Özlem Uğur 0000-0001-9257-085X

Kürşat Bora Çarman 0000-0002-4629-1873

Coşkun Yarar 0000-0001-7462-4578

Gönderilme Tarihi 23 Mayıs 2025
Kabul Tarihi 22 Temmuz 2025
Yayımlanma Tarihi 31 Ekim 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 25 Sayı: 3

Kaynak Göster

APA Yücel Şen, A. D., Baysal, A., Uğur, Ö., … Çarman, K. B. (2025). Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab. Çocuk Dergisi, 25(3), 172-175. https://doi.org/10.26650/jchild.2025.1704940
AMA Yücel Şen AD, Baysal A, Uğur Ö, Çarman KB, Yarar C. Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab. Çocuk Dergisi. Ekim 2025;25(3):172-175. doi:10.26650/jchild.2025.1704940
Chicago Yücel Şen, Arife Derda, Ahmet Baysal, Özlem Uğur, Kürşat Bora Çarman, ve Coşkun Yarar. “Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab”. Çocuk Dergisi 25, sy. 3 (Ekim 2025): 172-75. https://doi.org/10.26650/jchild.2025.1704940.
EndNote Yücel Şen AD, Baysal A, Uğur Ö, Çarman KB, Yarar C (01 Ekim 2025) Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab. Çocuk Dergisi 25 3 172–175.
IEEE A. D. Yücel Şen, A. Baysal, Ö. Uğur, K. B. Çarman, ve C. Yarar, “Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab”, Çocuk Dergisi, c. 25, sy. 3, ss. 172–175, 2025, doi: 10.26650/jchild.2025.1704940.
ISNAD Yücel Şen, Arife Derda vd. “Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab”. Çocuk Dergisi 25/3 (Ekim2025), 172-175. https://doi.org/10.26650/jchild.2025.1704940.
JAMA Yücel Şen AD, Baysal A, Uğur Ö, Çarman KB, Yarar C. Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab. Çocuk Dergisi. 2025;25:172–175.
MLA Yücel Şen, Arife Derda vd. “Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab”. Çocuk Dergisi, c. 25, sy. 3, 2025, ss. 172-5, doi:10.26650/jchild.2025.1704940.
Vancouver Yücel Şen AD, Baysal A, Uğur Ö, Çarman KB, Yarar C. Successful Treatment of MuSK Antibody–Positive Myasthenia Gravis with Rituximab. Çocuk Dergisi. 2025;25(3):172-5.