Choroidal metastasis as a rare feature of papillary thyroid carcinoma

A. Sauer, D. Gaucher, T. Bourcier, C. Speeg-Schatz
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Abstract

Department of Ophthalmology, Hôpitaux Universitaires de Strasbourg, Nouvel Hopital Civil, France Abstract Introduction Choroidal metastasis is a very rare clinical manifestation of thyroid cancer. The goal of our work is to report a case of late choroidal metastasis from papillary thyroid carcinoma. Case report A 59-year-old woman who had been treated for papillary thyroid carcinoma 3 years earlier presented for evaluation of vision loss in the right eye. A fundoscopic examination revealed a choroidal mass which had the typical characteristics of a metastatic lesion. After exclusion of any other neoplastic lesion, metastatic lesion from papillary thyroid carcinoma was diagnosed. The patient was treated with a combination of brachytherapy and chemotherapy. Despite this treatment, the patient complained about two other metastatic lesions (lung and hip) a few months later. Conclusion Papillary thyroid carcinoma can metastasise to the choroid many years after the initial diagnosis.
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脉络膜转移是甲状腺乳头状癌的罕见特征
摘要简介脉络膜转移是甲状腺癌中一种非常罕见的临床表现。我们的工作的目的是报告一例晚期脉络膜转移甲状腺乳头状癌。病例报告一名59岁妇女,3年前因甲状腺乳头状癌接受治疗,前来评估右眼视力下降。眼底镜检查发现脉络膜肿块,具有典型的转移性病变特征。排除其他肿瘤病变后,诊断为甲状腺乳头状癌转移灶。病人接受了近距离放疗和化疗的联合治疗。尽管接受了这种治疗,但几个月后,患者抱怨出现了另外两个转移性病变(肺和髋关节)。结论甲状腺乳头状癌可在初诊多年后转移至脉络膜。
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