Neurofibromatosis type 1 associated optic pathway glioma—a very-long-term follow-up

Author(s):  
Michael Kinori ◽  
Robert Listernick ◽  
Joel Charrow ◽  
Janice L. Zeid
2018 ◽  
Vol 20 (suppl_2) ◽  
pp. i145-i145
Author(s):  
Mariana Fernandes ◽  
João Passos ◽  
Daniela Garcez ◽  
Manuela Mafra ◽  
Maria Fátima Campos ◽  
...  

Author(s):  
Romain Touzé ◽  
Anthony Manassero ◽  
Dominique Bremond‐Gignac ◽  
Matthieu P. Robert

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Gentaro Kumagai ◽  
Naoki Echigoya ◽  
Kanichiro Wada ◽  
Toru Asari ◽  
Satoshi Toh ◽  
...  

Introduction: Vascularized fibular grafts (VFG) in the cervicothoracic spine have been used for patients with progressive neurofibromatosis (NF) type-1-related kyphosis, but the long-term outcomes of VFG with NF-1 are not well described. We describe the long-term follow-up of two cases of cervical kyphosis related to NF-1 treated with VFG in the cervical spine. Case Report: Case 1 was that of a 33-year-old man with a large neurofibroma at the back of his neck and an arteriovenous malformation at C2–7. The neurofibroma was resected by durotomy and intradural neurofibromas were extirpated through O-C6 laminectomy. Anterior fusion with VFG was performed 6 months later, and bone union was confirmed after 4 months. Cervical alignment was maintained with 50° kyphosis 15 years after the operation. The man suffered a subarachnoid hemorrhage 22 years after the operation. Case 2 was a 23-year-old woman with diastematomyelia at C6–T1 who was treated by anterior fusion with VFG at C4–T1. The diastematomyelia septum was resected through a C4–T1 laminectomy with simultaneous posterolateral fusion at C3–T2. Cervical alignment was maintained with 50° kyphosis 18 years later. The left vertebral artery ruptured and was embolized 10 years after the operation. Conclusion: Anterior fusion with VFG can achieve good bone union and maintains long-term alignment. However, it is important to watch for vascular events related to NF-1. Keywords: Vascularized fibular graft, cervical kyphosis, neurofibromatosis type 1.


2021 ◽  
Vol 221 ◽  
pp. 91-96 ◽  
Author(s):  
Michael Kinori ◽  
Sharon Armarnik ◽  
Robert Listernick ◽  
Joel Charrow ◽  
Janice Lasky Zeid

Author(s):  
A. Bolčeková ◽  
A. Hlavatá ◽  
A. Zat'ková ◽  
M. Némethová ◽  
M. Holobradá ◽  
...  

AbstractNeurofibromatosis type 1 (NF1) is one of the most common autosomal dominant disorders with mainly mild cutaneous manifestations. Some patients with NF1, however, develop severe complications such as progressive optic pathway glioma, plexiform neurofibroma or malignant peripheral nerve sheath tumour. Due to potentially progressive and asymptomatic course of the disease, patients with NF1 require a regular multidisciplinary follow-up in coordination with various specialties and early intervention. In this article, we summarise our long-term experience with multidisciplinary follow-up of NF1 patients in the Centre for Neurofibromatosis Type 1 patients at the Children's University Hospital in Bratislava.


2010 ◽  
Vol 55 (6) ◽  
pp. 1083-1088 ◽  
Author(s):  
Marta Campagna ◽  
Enrico Opocher ◽  
Elisabetta Viscardi ◽  
Milena Calderone ◽  
Savina Maria Severino ◽  
...  

2020 ◽  
Vol 43 (5) ◽  
pp. e179-e181
Author(s):  
F. Palma-Carvajal ◽  
H. González-Valdivia ◽  
J.P. Figueroa-Vercellino ◽  
C. Saavedra-Gutiérrez ◽  
C. Rovira-Zurriaga ◽  
...  

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