原发性甲状腺淋巴瘤的青少年桥本甲状腺炎和先天性耳聋

J. V. Heerden, J. Verlooy, K. Norga, T. Tousseyn, Yeleni Eelen
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引用次数: 0

摘要

背景:原发性甲状腺淋巴瘤在儿童和青少年中极为罕见。甲状腺恶性肿瘤的诊断通常是继发于其他甲状腺疾病,包括桥本甲状腺炎(HT)。病例介绍:这个病例描述了一个14岁的女孩,她有HT和先天性耳聋的背景,表现为迅速扩大的甲状腺多结节肿块。她接受了甲状腺全切除术,病理诊断为弥漫性大b细胞淋巴瘤。讨论:原发性甲状腺疾病是一种极为罕见的儿童疾病,通常表现为甲状腺肿大。桥本甲状腺炎与原发性甲状腺淋巴瘤之间的相关性在成人中已得到证实,但在儿科人群中尚未得到证实。我们的患者也有β地中海贫血和Usher综合征,然而,在文献中没有发现这些与原发性甲状腺淋巴瘤之间的相关性。结论:在甲状腺肿大或不明原因症状的鉴别诊断中,包括恶性肿瘤是很重要的,特别是在有综合征的情况下。需要进一步研究儿科人群中淋巴瘤和HT之间的关系。
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Primary Thyroid Lymphoma in an Adolescent with Hashimoto’s Thyroiditis and Congenital Deafness
Background: Primary thyroid lymphoma is extremely rare in children and adolescents. The diagnosis of thyroid malignancies is often made secondary to other thyroid pathologies including Hashimoto’s thyroiditis (HT). Case Presentation: This case describes a 14-year-old girl with a background of HT and congenital deafness that presented with a rapidly enlarging multinodular thyroid mass. She underwent a total thyroidectomy and a diffuse, large B-cell lymphoma was diagnosed on pathology. Discussion: Primary thyroid disease is an extremely rare disease in childhood, usually presenting as a rapidly enlarging goitre. The correlation between Hashimoto’s thyroiditis and primary thyroid lymphoma is well-established in adults but has not been verified in the paediatric population. Our patient also has βthalassemia and Usher syndrome, however, no correlation between these and primary thyroid lymphoma could be found in the literature. Conclusion: It is important to include malignancy in the differential diagnosis of thyroid enlargement or unexplained symptoms, especially in the presence of syndromes. Further research into the relation between lymphomas and HT in the paediatric population is needed.
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