Title of article
Giant mediastinal mass in a 3-year-old boy: A rare presentation of neurofibromatosis type I
Author/Authors
KARAMI, Hosseni Pediatric Hematology & Oncology Department - Thalassemia Research Center (TRC) - Hemoglobinopathy Institute - Mazandaran University of Medical Sciences - Sari, Iran , GHASEMI, Maryam Immunogenetics Research Center - Faculty of Medicine - Mazandaran University of Medical Sciences - Sari, Iran , TAHERI, Amirmasoud Medical Student- Faculty of Medicine - Mazandaran University of Medical Sciences - Sari, Iran , ROSTAMKOLAIE e, Faria Medical Student- Faculty of Medicine - Mazandaran University of Medical Sciences - Sari, Iran , ABBASKHANIAN, A Pediatrics Neurology - Clinical Research Development Unit of Bu-Ali Sina Hospital - Mazandaran University of Medical Sciences - Sari, Iran , NADERISORKI, Mohammad Pediatric Hematology & Oncology Department - Thalassemia Research Center (TRC) - Hemoglobinopathy Institute - Mazandaran University of Medical Sciences - Sari, Iran
Pages
5
From page
109
To page
113
Abstract
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease
diagnosed with the presentation of café-au-lait macules, skinfold
freckling, iris Lisch nodules, neurofibromas, osseous lesion, and
optic gliomas. Mediastinal mass as the first presentation of NF1 is
very rare, with a frequency of about 2.7%. Here, we present a rare
case of NF1 in a 3-year-old boy admitted with respiratory distress and
superior vena cava syndrome.
Keywords
Child , Superior vena cava syndrome , Mediastinal mass , Neurofibromatosis type 1
Journal title
Iranian Journal of Child Neurology (IJCN)
Serial Year
2021
Record number
2701466
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