[基底细胞痣综合征的神经系统表现。1例病例]
[Neurologic manifestations of basal cell nevomatosis. A case].
作者信息
Aumaître O, Sampoux P, Georget A M, Mondie J M, Thieblot P, Dordain G
出版信息
Presse Med. 1986 Nov 29;15(42):2105-7.
PMID:2954047
Abstract
The naevoid basal cell syndrome, also called Gorlin's syndrome, is a dysembryoplasia akin to the phakomatoses and which may affect the skin, the bones, the nervous system, the eyes, the endocrine glands and the genitalia. A case with numerous tumours and malformations is presented, together with a review of the literature.
摘要
痣样基底细胞癌综合征，也称为戈林综合征，是一种类似于 phakomatoses 的胚胎发育异常，可影响皮肤、骨骼、神经系统、眼睛、内分泌腺和生殖器。本文报告了一例伴有众多肿瘤和畸形的病例，并对相关文献进行了综述。
相似文献
1
[Neurologic manifestations of basal cell nevomatosis. A case].[基底细胞痣综合征的神经系统表现。1例病例]
Presse Med. 1986 Nov 29;15(42):2105-7.
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Meningioma associated with Gorlin's syndrome.
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[Basocellular nevomatosis: a syndrome of stomatological importance. Notes on 3 clinical cases].
Minerva Stomatol. 1982 Jul-Aug;31(4):443-8.
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Nevoid Basal Cell Carcinoma Syndrome and Hairy Skin Patches.
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Case report: nasopharyngeal rhabdomyosarcoma and Gorlin's naevoid basal cell carcinoma syndrome.病例报告：鼻咽横纹肌肉瘤与戈林痣样基底细胞癌综合征
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The cutaneous keratocyst: a rare hallmark of the nevoid basal cell carcinoma syndrome.皮肤角质囊肿：痣样基底细胞癌综合征的罕见特征。
Int J Surg Pathol. 2003 Jan;11(1):36. doi: 10.1177/106689690301100109.
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Naevoid basal cell carcinoma (Gorlin's) syndrome.
Aust N Z J Surg. 1993 May;63(5):413-5. doi: 10.1111/j.1445-2197.1993.tb00413.x.
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The basal cell nevus syndrome.基底细胞痣综合征。
Trans Pa Acad Ophthalmol Otolaryngol. 1982 Spring;35(1):8-12.
9
Bilateral epiretinal membranes in nevoid basal cell carcinoma syndrome.痣样基底细胞癌综合征中的双侧视网膜前膜。
Acta Ophthalmol Scand. 2004 Aug;82(4):488-90. doi: 10.1111/j.1395-3907.2004.0257.x.
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Gorlin's basal cell nevus syndrome.戈林基底细胞痣综合征。
Arch Otolaryngol Head Neck Surg. 1986 Jul;112(7):773-5. doi: 10.1001/archotol.1986.03780070085018.
引用本文的文献
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Two cases of nevoid basal cell carcinoma syndrome associated with meningioma caused by a PTCH1 or SUFU germline mutation.两例神经嵴来源的基底细胞痣综合征相关脑膜瘤，由 PTCH1 或 SUFU 种系突变引起。
Fam Cancer. 2012 Dec;11(4):565-70. doi: 10.1007/s10689-012-9548-0.
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