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Establishment of a Simple and Effective Rat Model for Intraoperative Parathyroid Gland Imaging
Published on: August 17, 2022
[Parathyroid glands involvement in multiple endocrine neoplasia]
E Târcoveanu1, D Niculescu, Elena Cotea
1Clinica I Chirurgie, Facultatea de Medicină, Universitatea de Medicină si Farmacie Gr.T. Popa Iaşi.
Summary
Multiple Endocrine Neoplasia (MEN) type I commonly involves parathyroid glands. Complete MEN I in younger patients requires subtotal parathyroidectomy, while incomplete forms in older patients may need adenoma resection with biopsy.
Area of Science:
- Endocrinology
- Surgical Oncology
- Genetics
Background:
- Multiple Endocrine Neoplasia (MEN) syndromes involve two or more endocrine glands.
- Parathyroid gland involvement is a hallmark of MEN type I (MEN I) and MEN type II.
- MEN I typically presents with parathyroid, pancreatic endocrine, and pituitary tumors, with parathyroid abnormalities being most frequent.
Observation:
- This study presents five cases of MEN I with parathyroid gland involvement.
- Three young patients (28-33 years) with familial MEN I had complete syndrome (parathyroid, pancreatic, and pituitary adenomas).
- Two older patients (57 and 68 years) presented with incomplete MEN I, involving parathyroid and pituitary glands.
Findings:
- Complete MEN I cases included parathyroid adenoma, gastrinoma/insulinoma, and pituitary adenoma.
- Incomplete MEN I cases featured hyperparathyroidism and pituitary tumors.
- Gastrinomas complicated surgical management and prognosis, with one patient experiencing peptic ulcer complications and another succumbing to endocrine disorders.
Implications:
- Parathyroid gland involvement is common in MEN, with distinct management strategies for complete (subtotal parathyroidectomy) and incomplete (adenoma resection with biopsy) forms.
- Gastrinomas significantly impact MEN I prognosis and surgical approach.
- Optimal management of MEN I necessitates a multidisciplinary team due to its complexity and challenging surgical considerations.
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