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Demographic and histological subtypes of Hurthle cell tumours of the thyroid in a South African setting
Malith, V; Bombil, I; Harran, N; Luvhengo, T. E.
Afiliación
  • Malith, V; s.af
  • Bombil, I; s.af
  • Harran, N; s.af
  • Luvhengo, T. E; s.af
S. Afr. j. surg. (Online) ; 56(3): 20-23, 2018. ilus
Article en En | AIM | ID: biblio-1271023
Biblioteca responsable: CG1.1
ABSTRACT

Background:

Report of Hurthle cells following fine needle aspiration cytology from a thyroid nodule raises possibility of Hurthle cell carcinoma (HCC), which is a distinct entity and accounts for 3­10% of thyroid malignancies.

Aim:

To determine if there are demographic and histopathological features which may be used to differentiate HCC from Hurthle cell adenoma (HCA).

Methods:

Histopathology records of patients who had thyroidectomy from January 2001 to October 2015 were reviewed. Data retrieved included indications for thyroidectomy, patients' demographics, histology and preoperative FNAC results.

Results:

At total of 2641 records were reviewed of which 25.6% (676/2641) were for neoplasms. 15.8% (107/676) of the neoplasms were Hurthle cell neoplasms (HCNs) and 25.2% (27/107) of HCNs were HCCs. 77.2% (71/92) of HCAs and 77.8% (21/27) of HCCs were from female patients. Preoperative FNAC results were available for 54.2% (58/107) and were suspicious of HCN in 12.1% (7/58). Average tumour size for HCCs and HCAs was 4.9 +/- 2.7 cm and 3.5 +/- 2.0 cm, respectively. The difference was statistically significant with a p-value of 0.016. The risk of malignancy increased from 11.1% in HCNs less than 1 cm to 53.8% for tumours which were greater than 4 cm in diameter.

Conclusion:

HCNs are more common in females. The likelihood of HCC rises as the size of the HCN increases. Malignancy rate exceeds 50% for HCNs which are greater than 4 cm in diameter
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Índice: AIM Asunto principal: Adenoma Oxifílico Idioma: En Revista: S. Afr. j. surg. (Online) Año: 2018 Tipo del documento: Article
Buscar en Google
Índice: AIM Asunto principal: Adenoma Oxifílico Idioma: En Revista: S. Afr. j. surg. (Online) Año: 2018 Tipo del documento: Article