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An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
FNA of thyroid granular cell tumor
1Department of Pathology, College Station Medical Center, Bryan, Texas.
Insights
This case report details a rare granular cell tumor in a thyroid nodule. Cytologic analysis revealed characteristic granular cells, aiding diagnosis through immunohistochemistry.
Area of Science:
- Endocrinology
- Cytopathology
- Surgical Pathology
Background:
- Granular cell tumors (GCTs) are uncommon neoplasms, with rare occurrences reported in the thyroid gland.
- Thyroid nodules are common, but GCTs present a diagnostic challenge due to their rarity and overlapping cytologic features with other thyroid lesions.
Observation:
- A case report of a 27-year-old woman presenting with a gradually enlarging thyroid nodule.
- Fine needle aspiration (FNA) cytology revealed a thyroid lesion with single and syncytial clusters of cells exhibiting abundant granular cytoplasm.
Findings:
- The cytologic findings were suggestive of GCT, but differential diagnoses included Hurthle cell lesions and histiocytic reparative processes.
- Immunohistochemical staining for S-100 protein and CD68 on a cell block preparation was crucial in confirming the diagnosis of granular cell tumor.
Implications:
- This case highlights the importance of considering rare entities like GCT in the differential diagnosis of thyroid nodules.
- Accurate cytologic and immunohistochemical evaluation is essential for the correct diagnosis and management of granular cell tumors of the thyroid.
- Understanding the cytologic features and diagnostic aids for GCT can improve diagnostic accuracy in thyroid FNA cytology.
Abstract:
Granular cell tumor rarely occurs in the thyroid. This case report describes the cytologic features of a granular cell tumor seen in a fine needle aspirate obtained from a 27-year-old woman with a gradually enlarging thyroid nodule. The aspirate showed single as well as syncytial clusters of cells with abundant granular cytoplasm. The differential diagnosis in this case included granular cell tumor, Hurthle cell lesion/neoplasm, and a histiocytic reparative process. Immunohistochemical studies, including S-100 protein and CD68, performed on a cell block preparation were helpful in supporting the diagnosis.
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