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考登综合征病例报告:使用超声外科吸引器进行唇部错构瘤的美容切除

Cowden Syndrome Case Report: Use of an Ultrasonic Surgical Aspirator for Cosmetic Removal of Lip Hamartomas.

作者信息

Montagne William, Wang Robert C

机构信息

Otolaryngology - Head and Neck Surgery, University of Nevada Las Vegas School of Medicine, Las Vegas, USA.

出版信息

Cureus. 2022 Oct 2;14(10):e29839. doi: 10.7759/cureus.29839. eCollection 2022 Oct.

DOI:10.7759/cureus.29839
PMID:36337787
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9625556/
Abstract

Cowden syndrome (CS) is an autosomal dominant condition that is relatively rare. CS patients can have tumors derived from all three germlines. They can present with mucocutaneous hamartomas or other benign tumors, and have an increased risk of malignancies of the thyroid, breast, kidney, GI tract, and skin. In our clinic, a 40-year-old CS patient presented for thyroidectomy after fine needle aspiration was suspicious for papillary thyroid carcinoma (PTC). Another major concern was the cosmetic appearance of her lips, which were diffusely covered with small hamartomas. We were able to remove these in a novel manner using a cavitron ultrasonic surgical aspirator (CUSA; Integra Lifesciences, Princeton, NJ, USA). Using the CUSA tangential to the lip surface allowed for removal of the hamartomas in a way that created a smooth and cosmetically appealing outcome for the patient. The use of an ultrasonic surgical aspirator is a novel way to cosmetically treat hamartomas of the lip for CS patients.

摘要

考登综合征(CS)是一种相对罕见的常染色体显性遗传病。CS患者可能会出现源自所有三个胚层的肿瘤。他们可能表现为皮肤黏膜错构瘤或其他良性肿瘤,并且患甲状腺、乳腺、肾脏、胃肠道和皮肤恶性肿瘤的风险增加。在我们的诊所,一名40岁的CS患者在细针穿刺怀疑为甲状腺乳头状癌(PTC)后前来接受甲状腺切除术。另一个主要问题是她的嘴唇外观,上面布满了小错构瘤。我们能够使用超声外科吸引器(CUSA;Integra Lifesciences,美国新泽西州普林斯顿)以一种新颖的方式将这些错构瘤切除。将CUSA与嘴唇表面相切使用,可以以一种为患者创造出平滑且美观效果的方式切除错构瘤。使用超声外科吸引器是一种为CS患者进行嘴唇错构瘤美容治疗的新颖方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/effef422cf06/cureus-0014-00000029839-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/b02a0092fc4b/cureus-0014-00000029839-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/49be169abc32/cureus-0014-00000029839-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/6a472e5dbf07/cureus-0014-00000029839-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/effef422cf06/cureus-0014-00000029839-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/b02a0092fc4b/cureus-0014-00000029839-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/49be169abc32/cureus-0014-00000029839-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/6a472e5dbf07/cureus-0014-00000029839-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d883/9625556/effef422cf06/cureus-0014-00000029839-i04.jpg

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本文引用的文献

1
PTEN Hamartoma Tumor Syndrome/Cowden Syndrome: Genomics, Oncogenesis, and Imaging Review for Associated Lesions and Malignancy.PTEN错构瘤综合征/考登综合征:相关病变及恶性肿瘤的基因组学、肿瘤发生机制与影像学综述
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Multidisciplinary surgical management of Cowden syndrome: Report of a case.考登综合征的多学科手术治疗:一例报告
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Genetic basis of Cowden syndrome and its implications for clinical practice and risk management.
考登综合征的遗传基础及其对临床实践和风险管理的意义。
Appl Clin Genet. 2016 Jul 13;9:83-92. doi: 10.2147/TACG.S41947. eCollection 2016.
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Genodermatosis Affecting the Skin and Mucosa of the Head and Neck: Clinicopathologic, Genetic, and Molecular Aspect--PTEN-Hamartoma Tumor Syndrome/Cowden Syndrome.影响头颈部皮肤和黏膜的遗传性皮肤病:临床病理、遗传及分子学方面——PTEN错构瘤综合征/考登综合征
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J Natl Cancer Inst. 2013 Nov 6;105(21):1607-16. doi: 10.1093/jnci/djt277. Epub 2013 Oct 17.
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A rare cause of oral papillomatous lesions: Cowden syndrome.口腔乳头状瘤病变的罕见病因:考登综合征。
Indian J Dermatol Venereol Leprol. 2012 Mar-Apr;78(2):230. doi: 10.4103/0378-6323.93666.
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Clin Cancer Res. 2012 Jan 15;18(2):400-7. doi: 10.1158/1078-0432.CCR-11-2283.
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