Giant care-au-lait macule in neurofibromatosis 1: A type 2 segmental manifestation of neurofibromatosis 1?

被引:13
作者
Yang, Chao-Chun [1 ,2 ]
Happle, Rudolf [3 ]
Chao, Sheau-Chiou [1 ]
Lee, Julia Yu-Yun [1 ]
Chen, WenChieh [4 ]
机构
[1] Natl Cheng Kung Univ, Dept Dermatol, Coll Med, Tainan 70101, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Inst Clin Med, Tainan 70101, Taiwan
[3] Univ Marburg, Dept Dermatol, Marburg, Germany
[4] Chang Gung Univ Coll Med, Chang Gung Mem Hosp, Kaohsiung Med Ctr, Dept Dermatol, Kaohsiung, Taiwan
关键词
DOMINANT SKIN DISORDERS; NF1; GENE; VONRECKLINGHAUSEN NEUROFIBROMATOSIS; PLEXIFORM NEUROFIBROMA; ALLELIC LOSS; MOSAICISM; MUTATION; HETEROZYGOSITY; PATIENT;
D O I
10.1016/j.jaad.2007.03.013
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Type 2 segmental manifestation of autosomal dominant dermatoses refers to pronounced segmental lesions superimposed on the ordinary nonsegmental phenotype, indicating loss of heterozygosity occurring at an early stage of embryogenesis. We describe a 20-year-old Taiwanese woman with typical lesions of neurofibromatosis type 1 (NF1) in the form of characteristic cafe-au-lait spots, neurofibromas, axillary freckling and Lisch nodules. in addition, a giant garment-like or "bathing-trunk" cafe-au-lait macule involved the lower half of the trunk, the buttocks, and parts of the thighs, being superimposed on the ordinary smaller spots of NF1. This large cafe-au-lait macule may be best explained as an example of type 2 segmental NF1. A novel mutation (3009delG) in exon 23 was also identified in this patient, which has not yet been described in sporadic and familial NF1.
引用
收藏
页码:493 / 497
页数:5
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