BACKGROUND: Multinucleated giant cell (MGC) present in a variety of non-neoplastic and neoplastic lesions of the thyroid on cytology samples. We aimed to investigate whether certain MGC features that can help us in routine cytopathology practice. METHOD: One hundred and thirty seven cases thyroid fine-needle aspiration material, which was diagnosed as indeterminate or malignant according to the Bethesda categorization, were reviewed. All cytomorphological features of the MGCs were documented. These features correlated with Bethesda categories and the final diagnosis of the subsequent surgical specimen. RESULTS: The presence of the MGCs was identified in 42% of the samples (58 cases-total 236 MGCs). Eighty eight of them (37%) had dense cytoplasm, 148 of them had foamy cytoplasm. The mean number of dense and foamy MGC per case was higher in the malignant category (3.2 for dense MGC and 6 for foamy MGC per case). All dense MGCs were found to be in patients with papillary thyroid carcinoma (PTC). Remarkably, follicular patterned lesions had less often dense MGC compared to papillary patterned lesions (16.6% and 46.8% respectively). We detected a nuclear irregularity in 49 dense MGC (55%), groove-like features in 24 dense MGC (27.2%), and presence of some material/cell in 8 dense MGC (9%). CONCLUSION: The presence of dense MGC is an important finding for guiding accurate Bethesda categorization, especially in indeterminate and malignant categories. Besides, the presence of some material or cell in MGCs cytoplasm can be an important indicator for the prognosis of the PTC cases. K E Y W O R D S cytology, indeterminate, malignant, multinucleated giant cells, papillary thyroid carcinoma 1 | INTRODUCTION Multinucleated giant cell (MGC) present in a variety of hyperplastic, inflammatory, and neoplastic lesions of the thyroid gland. 1-4 These cells are recognized as diagnostic criteria of the papillary thyroid carcinoma (PTC) however they are not specific. Their cell sizes, nuclear, and cytoplasmic features can vary in neoplastic conditions and the presence of MGC alone is not sufficient for definitive diagnosis. 5 Besides, there are some controversies about the origin of the cells. Some authors suggest that some MGCs may be epithelial, while others indicate that they are histiocytic lineage. 2-4,6-8 In daily practice, pathologists know the importance of finding MGC for malignancy diagnosis in thyroid cytology, however, they do not know exactly all the features of these cells that help us to