Thymic hyperplasia associated with primary Sjogren's syndrome cured by thymectomy

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Abstract

Thymus hyperplasia associated with Sjogren's syndrome is a rare morbid state. The present study described a 55-year-old woman who presented with a dryness of the oral cavity, and itchy eyes. Chest computed tomography identified a mass, measuring 4×2.5×2.5 cm, located at the anterior mediastinum. The mass was suspected as thymoma, thymic cyst, or teratoma, and resected by thymectomy. The postoperative pathological diagnosis was thymic lymphoid hyperplasia. After 1-year follow-up period, her sicca syndrome has been resolved. The present study records a successful case for thymectomy to treat the patients with thymic hyperplasia associated with primary Sjogren's syndrome (pSS).

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Xin, Y., Cai, H., Li, Y., & Cui, Y. (2017). Thymic hyperplasia associated with primary Sjogren’s syndrome cured by thymectomy. Journal of Thoracic Disease, 9(2), E130–E132. https://doi.org/10.21037/jtd.2017.02.24

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