Skytte Anne-Bine, Bojesen Anders, Bygum Anette
Klinisk Genetisk Afdeling, Vejle Sygehus, Sygehus Lillebælt, Kabbeltoft 25, 7100 Vejle.
Ugeskr Laeger. 2014 Jan 20;176(2):165-7.
Cowden syndrome is a rare autosomal dominant syndrome with a predisposition to cancer. We present a case of Cowden syndrome in a mother and her son, who were diagnosed with palmoplantar hyperkeratosis, macrocephaly and goitre. Early diagnosis is a challenge as the patients present with a variety of symptoms, but it is important because of the risk of cancer.
考登综合征是一种罕见的常染色体显性综合征,易患癌症。我们报告一例母亲及其儿子患考登综合征的病例,他们被诊断患有掌跖角化过度、巨头畸形和甲状腺肿。由于患者表现出多种症状,早期诊断具有挑战性,但鉴于癌症风险,早期诊断很重要。