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Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.

Ana Glavina   ORCID icon orcid.org/0000-0003-2137-9665 ; Department of Oral Medicine, School of Dental Medicine, University of Zagreb, Zagreb, Croatia

Puni tekst: engleski, PDF (150 KB) str. 260-260 preuzimanja: 74* citiraj
APA 6th Edition
Glavina, A. (2019). Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.. Acta Dermatovenerologica Croatica, 27 (4), 260-260. Preuzeto s https://hrcak.srce.hr/232334
MLA 8th Edition
Glavina, Ana. "Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.." Acta Dermatovenerologica Croatica, vol. 27, br. 4, 2019, str. 260-260. https://hrcak.srce.hr/232334. Citirano 28.10.2020.
Chicago 17th Edition
Glavina, Ana. "Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.." Acta Dermatovenerologica Croatica 27, br. 4 (2019): 260-260. https://hrcak.srce.hr/232334
Harvard
Glavina, A. (2019). 'Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.', Acta Dermatovenerologica Croatica, 27(4), str. 260-260. Preuzeto s: https://hrcak.srce.hr/232334 (Datum pristupa: 28.10.2020.)
Vancouver
Glavina A. Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.. Acta Dermatovenerol Croat. [Internet]. 2019 [pristupljeno 28.10.2020.];27(4):260-260. Dostupno na: https://hrcak.srce.hr/232334
IEEE
A. Glavina, "Gingival papillomatosis as the oral sign of Cowden's syndrome. A case report.", Acta Dermatovenerologica Croatica, vol.27, br. 4, str. 260-260, 2019. [Online]. Dostupno na: https://hrcak.srce.hr/232334. [Citirano: 28.10.2020.]

Sažetak

Abstract

Cowden's syndrome (CS) is a rare autosomal dominant, hereditary multiorgan disease with higher risk for malignancies (breast, thyroid, endometrium). Mucocutaneous lesions occur in 90% of cases and are characterized by facial trichilemmomas, oral mucosal papillomas and benign acral keratoses. A case of 39-year-old female patient with a chief complaint of "white spots" on the upper and lower attached gingiva accompanyed with skin changes on the face, hands and soles is presented. Her family medical history revealed that her mother had endometrial polyp and sister thyroid cancer. In her medical personal history, she reported follicular thyroid adenoma, thyroid abnormalities (i.e. lymphocytic thyroiditis), fibrocystic change and juvenile breast papillomatosis, lipoma, multiple fibromas and genitourinary tumors. Based on the extensive family and personal medical history, physical examination and histopathological findings, diagnostic criteria were fulfilled for the diagnosis of Cowden syndrome.

Hrčak ID: 232334

URI
https://hrcak.srce.hr/232334

Posjeta: 149 *