Reinders J W C, Koehler P J
Atrium Medisch Centrum, afd. Neurologie, Postbus 4446, 6401 CX Heerlen.
Ned Tijdschr Geneeskd. 2007 Aug 25;151(34):1891-5.
A Dutch family was diagnosed with familial schwannomatosis, a disorder that is distinct from neurofibromatosis (NF) type 1 and 2. The proband and 4 relatives had schwannomas on spinal roots, cranial nerves, plexuses, and peripheral nerves; no vestibular schwannomas were found. One of the affected relatives was later diagnosed with intracerebral glioma; schwannomas were not found. None of the living affected relatives had genomic defects affecting the NF2 gene. Large deletions in the proximal region of chromosome 22 were found in all resected schwannomas. Schwannomatosis can occur sporadically or be inherited. Pain is often the clinical manifestation of schwannomas. Resection should be reserved for tumours that are symptomatic or threaten to cause spinal cord compression.
一个荷兰家庭被诊断患有家族性神经鞘瘤病,这是一种与1型和2型神经纤维瘤病(NF)不同的疾病。先证者和4名亲属在脊神经根、颅神经、神经丛和周围神经上患有神经鞘瘤;未发现前庭神经鞘瘤。其中一名受影响的亲属后来被诊断患有脑内胶质瘤;未发现神经鞘瘤。在世的受影响亲属中没有发现影响NF2基因的基因组缺陷。在所有切除的神经鞘瘤中均发现22号染色体近端区域的大片段缺失。神经鞘瘤病可散发发生或遗传。疼痛通常是神经鞘瘤的临床表现。手术切除应仅用于有症状或可能导致脊髓压迫的肿瘤。