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伴有过多基底细胞癌的基底细胞痣综合征。

Basal cell nevus syndrome with excessive basal cell carcinomas.

作者信息

Kim Choon Soo, Na Young Cheon

机构信息

Department of Plastic and Reconstructive Surgery, Wonkwang University Hospital, Iksan, Korea.

出版信息

Arch Craniofac Surg. 2021 Apr;22(2):122-125. doi: 10.7181/acfs.2021.00136. Epub 2021 Apr 20.

DOI:10.7181/acfs.2021.00136
PMID:33957740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8107455/
Abstract

Basal cell nevus syndrome (BCNS), also known as basal cell carcinoma nevus syndrome, Gorlin syndrome, Gorlin-Goltz syndrome, and nevoid basal cell carcinoma, is a rare autosomal dominant disorder with a prevalence of approximately 1/60,000. A lower prevalence rate of 1/13,939,393 has also been reported in Korea. We report the case of a 40-year-old male patient with multiple black pigmented macules on the face that first appeared when he was a teenager. His clinical features of jaw cysts, bifid ribs, and calcification of the falx cerebri were fitting within the criteria for the diagnosis of BCNS. We excised all suspected macules and sent permanent biopsy. Most of the histological examinations of the biopsy samples taken during surgical excision of the face masses showed basal cell carcinomas. Ten months after the surgery, the patient has remained free from symptoms and is undergoing follow-up observation.

摘要

基底细胞痣综合征(BCNS),也称为基底细胞癌痣综合征、戈林综合征、戈林-戈尔茨综合征和痣样基底细胞癌,是一种罕见的常染色体显性疾病,患病率约为1/60,000。韩国也曾报道过较低的患病率,为1/13,939,393。我们报告了一例40岁男性患者,其面部有多个黑色色素沉着斑,这些斑在他青少年时期首次出现。他的颌骨囊肿、肋骨分叉和大脑镰钙化等临床特征符合BCNS的诊断标准。我们切除了所有疑似斑,并进行了永久活检。在手术切除面部肿物期间采集的活检样本的大多数组织学检查显示为基底细胞癌。手术后十个月,患者一直无症状,正在接受随访观察。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/eb51ffce023c/acfs-2021-00136f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/d7205a225682/acfs-2021-00136f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/413f084d0271/acfs-2021-00136f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/7ef921efbd99/acfs-2021-00136f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/289aad267fc0/acfs-2021-00136f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/139fd8798042/acfs-2021-00136f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/eb51ffce023c/acfs-2021-00136f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/d7205a225682/acfs-2021-00136f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/413f084d0271/acfs-2021-00136f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/7ef921efbd99/acfs-2021-00136f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/289aad267fc0/acfs-2021-00136f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/139fd8798042/acfs-2021-00136f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6083/8107455/eb51ffce023c/acfs-2021-00136f6.jpg

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Multiple nonmelanocytic skin cancers in multiple regions.多个区域出现多发性非黑素细胞性皮肤癌。
Arch Craniofac Surg. 2020 Jun;21(3):188-192. doi: 10.7181/acfs.2020.00073. Epub 2020 Jun 29.
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Manifestations of Gorlin-Goltz syndrome.戈林-戈尔茨综合征的表现。
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Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome.PTCH2 基因的移码突变可导致结节性基底细胞癌综合征。
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