1型神经纤维瘤病中的弗雷综合征
Frey syndrome in neurofibromatosis 1.
作者信息
Ibrahim Laila Farah, Brenner Clare, McMenamin Joe, Webb David
机构信息
Department of Neonatology, Cork University Maternity Hospital, Cork, Ireland.
出版信息
BMJ Case Rep. 2011 Mar 15;2011:bcr0920092286. doi: 10.1136/bcr.09.2009.2286.
Abstract
A healthy 18-month-old girl presented with a history of intermittent hemifacial flushing when eating. Her symptom seemed to be exclusively triggered by chewing. Examination revealed cutaneous features of neurofibromatosis type 1 (NF1) and mild facial asymmetry. Imaging confirmed cerebral vacuolisation changes seen in NF1 and a left facial plexiform neurofibroma involving the parotid gland. This is the first reported case of Frey syndrome complicating NF1.
摘要
一名18个月大的健康女孩出现进食时间歇性半侧面部潮红的病史。她的症状似乎仅由咀嚼引发。检查发现有1型神经纤维瘤病（NF1）的皮肤特征和轻度面部不对称。影像学检查证实了NF1中所见的脑空泡化改变以及累及腮腺的左侧面部丛状神经纤维瘤。这是首例报道的并发NF1的 Frey综合征病例。
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