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DOI: 10.1055/a-2593-9749
The Interesting Case

Neuroimaging and Metabolic Features of Optic Pathway Glioma in a Child with Neurofibromatosis Type 1: Low-Grade Glioma Transformation in the Left Optic Radiation

Neuroimaging und metabolische Merkmale des Sehbahnglioms bei einem Kind mit Neurofibromatose Typ 1: Niedriggradige Gliomtransformation in der linken Sehbahnstrahlung
Samira Sijahovic
1   Radiology, Bezmialem Vakif University, Istanbul, Türkiye (Ringgold ID: RIN221265)
,
2   Radiology, Maltepe University, Istanbul, Türkiye (Ringgold ID: RIN52981)
,
Bahar Atasoy
1   Radiology, Bezmialem Vakif University, Istanbul, Türkiye (Ringgold ID: RIN221265)
,
Ümmühan Ebru Karabulut
1   Radiology, Bezmialem Vakif University, Istanbul, Türkiye (Ringgold ID: RIN221265)
,
Mehmet Nuri Belge
1   Radiology, Bezmialem Vakif University, Istanbul, Türkiye (Ringgold ID: RIN221265)
,
Defne Şahin
1   Radiology, Bezmialem Vakif University, Istanbul, Türkiye (Ringgold ID: RIN221265)
,
Alpay Alkan
1   Radiology, Bezmialem Vakif University, Istanbul, Türkiye (Ringgold ID: RIN221265)
› Author Affiliations
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Introduction

Neurofibromatosis type 1 (NF1) is the most common single-gene genetic disorder, affecting 1/3500 children [1]. The NF-1 gene responsible for the disease is located on the length of chromosome 17 [2] [3]. NF-1 affects various organ systems, including the skin, nervous, endocrine, eye, and skeleton [2] [3]. Patients with NF-1 have a high predisposition to develop both benign and malignant tumors, including optic pathway gliomas (OPG), which are seen in 15–20% of NF-1 patients. Optic gliomas (OPG) represent 1–2% of all brain tumors, with most being benign and associated with NF-1 [1] [4] [5].



Publication History

Received: 04 October 2024

Accepted after revision: 23 April 2025

Article published online:
28 May 2025

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