表现为吞咽困难的丛状神经纤维瘤病。
Plexiform neurofibromatosis presenting as dysphagia.
作者信息
Gupta A K, Dey Pranab
机构信息
Dept. of Otolaryngology and Head and Neck Surgery, PGIMER, 160012 Chandigarh.
出版信息
Indian J Otolaryngol Head Neck Surg. 2006 Apr;58(2):183-5. doi: 10.1007/BF03050783.
Abstract
Plexiform neurofibromatosis is a autosomal dominant disease characterized by multiple cafe aulait spots, cutaneous neurofibromatosis, CMS tumours and skeletal abnormalities. We report a child with plexiform neurofibromatosis presenting with dysphagia, an unsual presentation.
摘要
丛状神经纤维瘤病是一种常染色体显性疾病，其特征为多发咖啡牛奶斑、皮肤神经纤维瘤、CMS肿瘤和骨骼异常。我们报告了一名患有丛状神经纤维瘤病的儿童，该患儿表现为吞咽困难，这是一种不寻常的表现。
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本文引用的文献
1
NEUROGENIC TUMORS OF THE HEAD AND NECK.头颈部神经源性肿瘤
Laryngoscope. 1964 Aug;74:1037-59. doi: 10.1288/00005537-196408000-00002.
2
Neurofibromatosis in childhood.儿童神经纤维瘤病
J Pediatr. 1970 Mar;76(3):339-46. doi: 10.1016/s0022-3476(70)80472-3.
3
Skin manifestations of von Recklinghausen's disease and associated tumors (neurofibromatosis).
Am Surg. 1965 Nov;31(11):729-40.
4
Head and neck manifestations of neurofibromatosis.神经纤维瘤病的头颈部表现
Laryngoscope. 1986 Jul;96(7):732-7. doi: 10.1288/00005537-198607000-00005.
5
NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update.美国国立卫生研究院会议。神经纤维瘤病1型（冯雷克林霍增氏病）和神经纤维瘤病2型（双侧听神经纤维瘤病）。最新进展。
Ann Intern Med. 1990 Jul 1;113(1):39-52. doi: 10.7326/0003-4819-113-1-39.
6
Plexiform neurofibroma of the head and neck.
Am J Surg. 1979 Oct;138(4):517-20. doi: 10.1016/0002-9610(79)90411-2.
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