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Galectin-3 and Ki-67 expression in multiglandular parathyroid lesions
Enrico Saggiorato1, Nicoletta Bergero, Marco Volante
1Section of Endocrinology, University of Turin, Italy.
American Journal of Clinical Pathology
|June 7, 2006
Summary
Galectin-3 is not a reliable marker for distinguishing benign from malignant parathyroid growths in multiglandular disease. Secondary hyperplasia shows unexpected galectin-3 positivity, limiting its diagnostic value.
Area of Science:
- Endocrinology
- Surgical Pathology
- Oncology
Background:
- Parathyroid lesions, both hyperplastic and neoplastic, exhibit overlapping features, necessitating reliable markers for malignancy diagnosis.
- Galectin-3 has shown promise as a marker for malignancy in uniglandular parathyroid diseases.
Purpose of the Study:
- To investigate the immunoexpression of galectin-3 and Ki-67 in multiglandular parathyroid hyperplastic lesions.
- To compare these markers in primary, secondary, and tertiary hyperplasia against parathyroid adenomas and carcinomas.
Main Methods:
- Analysis of 63 multiglandular lesions (primary, secondary, tertiary hyperplasia) and controls (45 adenomas, 24 carcinomas).
- Immunohistochemical assessment for galectin-3 and Ki-67 expression.
Main Results:
- Hyperplastic lesions of primary nonfamilial and tertiary hyperparathyroidism, along with adenomas, were galectin-3 negative.
- Carcinomas were galectin-3 positive.
- Secondary and familial primary hyperplasia showed surprising galectin-3 positivity in approximately two-thirds of cases.
- All hyperplastic lesions demonstrated a low Ki-67 index, indicating low proliferative potential.
Conclusions:
- Galectin-3 reactivity in secondary hyperplasia is unexplained and reduces its utility in differentiating benign from malignant parathyroid nodules in multiglandular disease.
- Ki-67 index is low across all hyperplastic lesions, suggesting limited proliferative capacity.