A Case with Cowden Syndrome

被引：0

作者：

Parlak, Nehir ^{[1
]}

Akay, Bengu Nisa ^{[2
]}

Kundakci, Nihal ^{[2
]}

机构：

[1] Prof Dr Celal Ertug Etimesgut Devlet Hastanesi, Deri & Zuhrevi Hastaliklar Klin, Ankara, Turkey

[2] Ankara Univ, Tip Fak, Deri & Zuhrevi Hastaliklar Anabilim Dali, TR-06100 Ankara, Turkey

来源：

TURK DERMATOLOJI DERGISI-TURKISH JOURNAL OF DERMATOLOGY | 2015年 / 9卷 / 02期

关键词：

Cowden syndrome; intestinal polyposis; macrocephaly; papilloma; PTEN mutation; hereditary cancer syndromes;

D O I：

10.4274/tdd.2009

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Cowden syndrome is an autosomal dominant rare inherited disorder characterized by multiple hamartomas in variety of tissues from all three embryonic layers. Mucocutaneous lesions like facial trichilemmomas, acral keratoses, papillomatous papules, also macrocephaly and malignancies including breast, tyhroid and endometrial carcinoma are hallmark of the disease. Here we report a 47-year-old male patient with mucucutaneous lesions, gastrointestinal polyposis and macrocephaly diagnosed as Cowden syndrome.

引用

页码：92 / 95

页数：4

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