Thyroid medullary carcinoma in a teenager with Cowden syndrome

被引:7
作者
Koksal, Yavuz
Sahin, Mustafa
Koksal, Hande
Orhan, Didehan
Unal, Ekrem [1 ]
Alagoz, Engin
机构
[1] Selcuk Univ, Meram Med Fac, Dept Pediat, Konya, Turkey
[2] Selcuk Univ, Meram Med Fac, Dept Pediat Oncol, Konya, Turkey
[3] Selcuk Univ, Meram Med Fac, Dept Gen Surg, Konya, Turkey
[4] NET GOZ Med Ctr, Konya, Turkey
[5] Univ Hacettepe, Fac Med, Dept Pediat, Pathol Unit, TR-06100 Ankara, Turkey
[6] Gulhane Mil Med Acad, Ankara, Turkey
关键词
child; Cowden syndrome; thyroid medullary carcinoma; SYNDROME PLEASE STAND; DISEASE; WILL;
D O I
10.1097/MLG.0b013e318058a0b7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Cowden syndrome is a multisystemic cancer predisposition disorder, in which the mucocutaneous lesions are the most constant features. We present a case of Cowden syndrome in a teenage boy with hyperkeratotic papules of the facial skin, especially on the eyelids, with episcleritis, proptosis, and papillomatous lesions on the tip of the tongue and lip mucosa. In addition, two nodules in the thyroid gland were detected. On laboratory examination, the carcinoembryonic antigen (CEA) was 34 ng/mL (normal limits: 0-3 ng/mL). Total thyroidectomy was performed. Histopathologic examination of the specimen revealed thyroid medullary carcinoma. After operation, levels of CEA decreased to normal limits.
引用
收藏
页码:1180 / 1182
页数:3
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