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Published on: July 14, 2023
Primary hyperparathyroidism with thyroid hemiagenesis.
Kenichi Sakurai1, Sadao Amano, Katsuhisa Enomoto
1Division of Breast and Endocrine Surgery, Department of Surgery, Nihon University School of Medicine, Tokyo, Japan. ksakurai@med.nihon-u.ac.jp
Thyroid hemiagenesis, a rare congenital anomaly, was incidentally discovered during evaluation for primary hyperparathyroidism in a male patient. Surgical confirmation revealed right thyroid lobe agenesis and a parathyroid adenoma.
Area of Science:
- Endocrinology
- Surgical Pathology
- Radiology
Background:
- Thyroid hemiagenesis is an exceptionally rare congenital condition characterized by the incomplete development of one thyroid lobe.
- Primary hyperparathyroidism is a condition often associated with parathyroid gland abnormalities and can present with symptoms like urinary lithiasis.
Observation:
- A 42-year-old male with urinary lithiasis presented with elevated serum calcium and intact parathyroid hormone levels, suggesting primary hyperparathyroidism.
- Imaging studies, including computed tomography and ultrasonography, revealed the absence of the right thyroid lobe and identified a mass on the left thyroid lobe.
Findings:
- The patient underwent a left lower parathyroidectomy for a suspected parathyroid adenoma.
- Pathological examination confirmed the parathyroid adenoma and corroborated the incidental finding of right thyroid hemiagenesis, including the absence of right parathyroid glands.
Implications:
- This case highlights the importance of recognizing rare congenital anomalies like thyroid hemiagenesis during the diagnostic workup of endocrine disorders.
- The incidental finding underscores the utility of cross-sectional imaging in identifying unexpected anatomical variations.
- Successful surgical management of the parathyroid adenoma in the context of thyroid hemiagenesis demonstrates favorable patient outcomes.
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