Diffuse Sclerosing Variant of Papillary Thyroid Carcinoma in a Child: A Case Report.
Seung Hee ByunSun Kyoung YouSeong Su KangKyung-Sook ShinJeong Eun LeePublished in: Taehan Yongsang Uihakhoe chi (2020)
The diffuse sclerosing variant of papillary thyroid carcinoma (DSPTC) is uncommon. Herein, we report a rare case of DSPTC in a 9-year-old girl who initially presented with a painless diffuse goiter. Thyroid peroxidase antibody testing yielded positive results, and the initial clinical diagnosis was Hashimoto's thyroiditis. However, thyroid ultrasonography revealed characteristic findings of DSPTC, which was confirmed through the postoperative histopathological diagnosis. Although thyroid cancers are rare in the pediatric population, DSPTC should be included in the differential diagnosis of goiter in these patients. Moreover, ultrasonography may prevent a diagnostic delay and facilitate the detection of a concomitant malignancy.
Keyphrases
- rare case
- low grade
- end stage renal disease
- lymph node
- lymph node metastasis
- magnetic resonance imaging
- chronic kidney disease
- ejection fraction
- contrast enhanced
- newly diagnosed
- patients undergoing
- mental health
- prognostic factors
- peritoneal dialysis
- hydrogen peroxide
- single cell
- computed tomography
- patient reported outcomes
- magnetic resonance