Werner syndrome associated with poorly differentiated thyroid carcinoma and systemic sclerosis-like skin manifestations: A case report.

Eri Sugawara, Yuhei Shibata, Kazuaki Katsumata
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Abstract

Werner syndrome (WS) is an autosomal recessive disorder characterised by premature ageing. WS patients often experience scleroderma-like manifestation including skin sclerosis and skin ulcer, making it difficult to differentiate WS from systemic sclerosis (SSc). Moreover, there is a high incidence of malignancy and arteriosclerosis-related disease in WS patients. We herein describe a 36-year-old woman with WS who had poorly differentiated thyroid carcinoma, one of the rare phenotypes of thyroid tumour. This case suggested the importance to distinguish WS from SSc and early diagnosis of malignancy.

韦纳综合征伴有分化不良的甲状腺癌和系统性硬化症样皮肤表现:病例报告。
维尔纳综合征(WS)是一种以早衰为特征的常染色体隐性遗传疾病。WS 患者通常会出现硬皮病样表现,包括皮肤硬化和皮肤溃疡,因此很难将 WS 与系统性硬化症(SSc)区分开来。此外,WS 患者中恶性肿瘤和动脉硬化相关疾病的发病率也很高。我们在此描述了一名患有甲状腺分化不良癌(甲状腺肿瘤的罕见表型之一)的 36 岁 WS 女性患者。该病例提示了区分WS和SSc以及早期诊断恶性肿瘤的重要性。
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