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戈林-戈尔茨综合征。

Gorlin-Goltz syndrome.

作者信息

Jawa Deepti Singh, Sircar Keya, Somani Rani, Grover Neeraj, Jaidka Shipra, Singh Sanjeet

机构信息

Department of Pedodontics and Preventive Dentistry, D.J. College of Dental Sciences and Research, Niwari Road, Modinagar, Uttar Pradesh, India.

出版信息

J Oral Maxillofac Pathol. 2009 Jul;13(2):89-92. doi: 10.4103/0973-029X.57677.

DOI:10.4103/0973-029X.57677
PMID:21887009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3162868/
Abstract

Gorlin-Goltz syndrome is an autosomal dominant inherited disorder characterized by the presence of multiple odontogenic keratocysts along with various cutaneous, dental, osseous, ophthalmic, neurological, and sex organ abnormalities. Early diagnosis is essential as it may progress to aggressive basal cell carcinomas and neoplasias. Gorlin-Goltz syndrome has rarely been reported from India. We report here one such patient, diagnosed at a rural hospital.

摘要

戈林-戈尔茨综合征是一种常染色体显性遗传性疾病，其特征为存在多个牙源性角化囊肿以及各种皮肤、牙齿、骨骼、眼科、神经和性器官异常。早期诊断至关重要，因为它可能发展为侵袭性基底细胞癌和肿瘤。印度鲜有关于戈林-戈尔茨综合征的报道。我们在此报告一名在农村医院确诊的此类患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/b940aaef7842/JOMFP-13-89-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/702b38211f23/JOMFP-13-89-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/e13028ca1c89/JOMFP-13-89-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/f31410509298/JOMFP-13-89-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/cc4f042fd080/JOMFP-13-89-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/9cbf5fe48c9a/JOMFP-13-89-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/b940aaef7842/JOMFP-13-89-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/702b38211f23/JOMFP-13-89-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/e13028ca1c89/JOMFP-13-89-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/f31410509298/JOMFP-13-89-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/cc4f042fd080/JOMFP-13-89-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/9cbf5fe48c9a/JOMFP-13-89-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc5/3162868/b940aaef7842/JOMFP-13-89-g006.jpg

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本文引用的文献

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Atypical gorlin's syndrome.非典型基底细胞痣综合征
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Jaw cyst-Basal cell nevus-Bifid rib syndrome: a case report.颌骨囊肿-基底细胞痣-肋骨分叉综合征：一例报告
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Analysis of the neoplastic nature and biological potential of sporadic and nevoid basal cell carcinoma syndrome-associated keratocystic odontogenic tumor.散发性及痣样基底细胞癌综合征相关牙源性角化囊性瘤的肿瘤性质及生物学潜能分析
戈林-戈尔茨综合征全颞下颌关节置换术中的放射学及外科手术考量与替代方案
Diagnostics (Basel). 2025 May 2;15(9):1158. doi: 10.3390/diagnostics15091158.
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Recurrent Metastatic Basal Cell Carcinomas of the Face in a Patient with Gorlin-Goltz Syndrome.一名患有戈林-戈尔茨综合征患者面部复发性转移性基底细胞癌
Curr Oncol. 2025 Mar 26;32(4):193. doi: 10.3390/curroncol32040193.
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Non-Melanoma Skin Cancer: Assessing the Systemic Burden of the Disease.非黑色素瘤皮肤癌：评估该疾病的全身负担。
Cancers (Basel). 2025 Feb 19;17(4):703. doi: 10.3390/cancers17040703.
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Indian J Otolaryngol Head Neck Surg. 2024 Feb;76(1):1255-1259. doi: 10.1007/s12070-023-04252-9. Epub 2023 Oct 15.
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Gorlin-Goltz Syndrome: A Case Series.戈林-戈尔茨综合征：病例系列
Cureus. 2023 Sep 21;15(9):e45656. doi: 10.7759/cureus.45656. eCollection 2023 Sep.
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DNA Damage Response Mechanisms in Head and Neck Cancer: Significant Implications for Therapy and Survival.头颈部癌症中的 DNA 损伤反应机制：对治疗和生存的重要影响。
Int J Mol Sci. 2023 Feb 1;24(3):2760. doi: 10.3390/ijms24032760.
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Photodynamic therapy in pediatric age: Current applications and future trends.儿童期的光动力疗法：当前应用与未来趋势。
Front Pharmacol. 2022 Aug 16;13:879380. doi: 10.3389/fphar.2022.879380. eCollection 2022.
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J Oral Maxillofac Pathol. 2020 Sep-Dec;24(3):591. doi: 10.4103/0973-029X.190048. Epub 2021 Jan 9.
J Oral Pathol Med. 2007 Oct;36(9):550-4. doi: 10.1111/j.1600-0714.2007.00578.x.
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Indian J Pathol Microbiol. 2006 Oct;49(4):578-80.
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Nevoid basal cell carcinoma syndrome.痣样基底细胞癌综合征
Indian J Dent Res. 2006 Jan-Mar;17(1):50-3. doi: 10.4103/0970-9290.29891.
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[Clinical and genetic study in 22 patients with basal cell nevus syndrome].22例基底细胞痣综合征患者的临床与遗传学研究
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