Neuroblastoma in a Patient With Spinal Muscular Atrophy Type I: Is It Just a Coincidence?

SAĞ E., SEN H. S., HALİLOGLU G., YALÇIN B., Kutluk T.

JOURNAL OF CHILD NEUROLOGY, cilt.30, sa.8, ss.1075-1078, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 30 Sayı: 8
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1177/0883073814542950
  • Dergi Adı: JOURNAL OF CHILD NEUROLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.1075-1078
  • Hacettepe Üniversitesi Adresli: Evet

Özet

Spinal muscular atrophy is an autosomal recessive disorder characterized by progressive degeneration of anterior horn cells of the spinal cord resulting in hypotonia, skeletal muscle atrophy, and weakness. Herein, we report a 4-month-old male infant who presented to our hospital with an abdominal mass that was diagnosed as neuroblastoma and spinal muscular atrophy type I. We would like to discuss the course and differential diagnosis with an algorithm leading to the diagnosis in this peculiar patient. To our knowledge, coexistence of spinal muscular atrophy type I and neuroblastoma is defined for the first time in the literature.