J. V. Heerden, J. Verlooy, K. Norga, T. Tousseyn, Yeleni Eelen
{"title":"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","authors":"J. V. Heerden, J. Verlooy, K. Norga, T. Tousseyn, Yeleni Eelen","doi":"10.31487/j.cor.2020.05.11","DOIUrl":null,"url":null,"abstract":"Background: Primary thyroid lymphoma is extremely rare in children and adolescents. The diagnosis of\nthyroid malignancies is often made secondary to other thyroid pathologies including Hashimoto’s thyroiditis\n(HT).\nCase Presentation: This case describes a 14-year-old girl with a background of HT and congenital deafness\nthat presented with a rapidly enlarging multinodular thyroid mass. She underwent a total thyroidectomy and\na diffuse, large B-cell lymphoma was diagnosed on pathology.\nDiscussion: Primary thyroid disease is an extremely rare disease in childhood, usually presenting as a\nrapidly enlarging goitre. The correlation between Hashimoto’s thyroiditis and primary thyroid lymphoma\nis 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\ncould be found in the literature.\nConclusion: It is important to include malignancy in the differential diagnosis of thyroid enlargement or\nunexplained symptoms, especially in the presence of syndromes. Further research into the relation between\nlymphomas and HT in the paediatric population is needed.","PeriodicalId":10487,"journal":{"name":"Clinical Oncology and Research","volume":"20 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Primary Thyroid Lymphoma in an Adolescent with Hashimoto’s Thyroiditis and Congenital Deafness\",\"authors\":\"J. V. Heerden, J. Verlooy, K. Norga, T. Tousseyn, Yeleni Eelen\",\"doi\":\"10.31487/j.cor.2020.05.11\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Primary thyroid lymphoma is extremely rare in children and adolescents. The diagnosis of\\nthyroid malignancies is often made secondary to other thyroid pathologies including Hashimoto’s thyroiditis\\n(HT).\\nCase Presentation: This case describes a 14-year-old girl with a background of HT and congenital deafness\\nthat presented with a rapidly enlarging multinodular thyroid mass. She underwent a total thyroidectomy and\\na diffuse, large B-cell lymphoma was diagnosed on pathology.\\nDiscussion: Primary thyroid disease is an extremely rare disease in childhood, usually presenting as a\\nrapidly enlarging goitre. The correlation between Hashimoto’s thyroiditis and primary thyroid lymphoma\\nis 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\\ncould be found in the literature.\\nConclusion: It is important to include malignancy in the differential diagnosis of thyroid enlargement or\\nunexplained symptoms, especially in the presence of syndromes. Further research into the relation between\\nlymphomas and HT in the paediatric population is needed.\",\"PeriodicalId\":10487,\"journal\":{\"name\":\"Clinical Oncology and Research\",\"volume\":\"20 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-05-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Clinical Oncology and Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31487/j.cor.2020.05.11\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.cor.2020.05.11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.