Diagnostic models for predicting malignancy in thyroid nodules classified as Bethesda Category III in an endemic region


Kasap Z., KURT B., Özsağır E., ERCİN M. E., GÜNER A.

Diagnostic Cytopathology, cilt.52, sa.4, ss.200-210, 2024 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 52 Sayı: 4
  • Basım Tarihi: 2024
  • Doi Numarası: 10.1002/dc.25270
  • Dergi Adı: Diagnostic Cytopathology
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, CAB Abstracts, EMBASE, MEDLINE, Veterinary Science Database
  • Sayfa Sayıları: ss.200-210
  • Anahtar Kelimeler: atypia of undetermined significance (AUS), Bethesda, cytopathology, factor analysis, fine needle aspiration, risk of malignancy (ROM), thyroid nodule
  • Karadeniz Teknik Üniversitesi Adresli: Evet

Özet

Background: This study aims to develop a diagnostic model to help physicians determine whether thyroid nodules categorized as atypia of undetermined significance (AUS) in category III of the Bethesda system are benign or malignant preoperatively. To create a diagnostic model for predicting thyroid nodules' benign or malignant with AUS cytology based on clinical, ultrasonographic, and cytopathological findings. Methods: This is a retrospective cohort study involving patients (>19) at risk of thyroid cancer who had thyroidectomy after an AUS cytology. The dataset consists of 53 variables 204 nodules from 183 patients. Binary logistic regression and factor analysis methods were used to identify risk factors for malignancy. Finally, four prediction models were developed using different approaches, based on clinical, pathological clinical + pathological, and the factors. Results: A total of 88 (48.1%) of 183 patients diagnosed with AUS were benign and 95 (51.9%) the malignant. After determining risk factors, four prediction models were developed based on different approaches to assist physicians in deciding to detect AUS nodules early. It was seen that bilaterality was found to be a risk factor for malignancy in the clinical model (pbilaterality =.03) and it was also seen that the pathological variables pale chromatin and irregular contours in the oncocyte variables were risk factors for malignancy (ppalechromatin =.02, pirregularcontoursintheoncocyte =.04). The best model obtained sensitivity and specificity values are 73% and 87% based on clinical and pathological variables. Conclusion: This comprehensive study may provide a more in-depth understanding of AUS and make a notable contribution to healthcare professionals before surgery.