scholarly journals A rare case report of neurofibromatosis type 1 in a 12-year-old child: A 15-month follow-up

2020 ◽  
Vol 24 (4) ◽  
pp. 106
Author(s):  
Srinivas Nallanchakrava ◽  
ManojKumar Mallela ◽  
VShiva Kumar Jeenepalli ◽  
HM Niharika
Keyword(s):  
Case Report ◽  
Neurofibromatosis Type 1 ◽  
Rare Case ◽  
Neurofibromatosis Type ◽  
Rare Case Report

scholarly journals Optic Nerve Tortuosity in Neurofibromatosis Type 1: A Rare Case Report

2020 ◽  
pp. 1-4
Author(s):  
Dilek Top Karti ◽  
Omer Karti ◽  
Ali Murat Koç ◽  
Neşe Çelebisoy
Keyword(s):  
Case Report ◽  
Optic Nerve ◽  
Neurofibromatosis Type 1 ◽  
Rare Case ◽  
Neurofibromatosis Type ◽  
Rare Case Report

scholarly journals C1q nephropathy in a patient of neurofibromatosis Type 1: A rare case report

2019 ◽  
Vol 0 (0) ◽  
pp. 0 ◽  
Author(s):  
UT Varyani ◽  
NM Shah ◽  
PR Shah ◽  
VB Kute ◽  
MR Balwani ◽  
...  
Keyword(s):  
Case Report ◽  
Neurofibromatosis Type 1 ◽  
Rare Case ◽  
Neurofibromatosis Type ◽  
C1q Nephropathy ◽  
Rare Case Report

A rare case report of coexistent neurofibromatosis type 1 with sickle cell beta-plus thalassaemia

2020 ◽  
Vol 9 (1) ◽  
pp. 45
Author(s):  
Naval Chandra ◽  
PrabhuKiran Vanka ◽  
Raviteja Tejavath ◽  
D Swaroopa ◽  
MV S. Subbalaxmi ◽  
...  
Keyword(s):  
Case Report ◽  
Sickle Cell ◽  
Neurofibromatosis Type 1 ◽  
Rare Case ◽  
Neurofibromatosis Type ◽  
Rare Case Report

scholarly journals Spinal schwannomatosis of the cauda equina in the absence of neurofibromatosis: case report and treatment strategies

2017 ◽  
Vol 31 (1) ◽  
pp. 47-53
Author(s):  
Dana Turliuc ◽  
A. Cucu ◽  
R. Sandu ◽  
Gabriela Dumitrescu ◽  
Claudia Costea
Keyword(s):  
Case Report ◽  
Neurofibromatosis Type 1 ◽  
Treatment Strategy ◽  
Cauda Equina ◽  
Treatment Strategies ◽  
Neurofibromatosis Type ◽  
Rare Tumor ◽  
Multiple Schwannomas

AbstractSchwannomatosis is a rare tumor syndrome characterized by the presence of multiple benign non-vestibular, non-intradermal schwannomas and by the absence of neurofibromatosis type 1 or 2 syndromes. Multiple schwannomas are clinically and genetically distinct from neurofibromatosis, and the main treatment in case of symptomatic lesions is represented by surgical resection. In case of asymptomatic lesions, the indicated treatment is neuroimaging follow-up (MRI). We are presenting the case of a patient with three schwannomas of the cauda equina, as well as the treatment strategy in the case of this rare pathology.

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