Tumour of the parafollicular cells which secrete calcitonin (C-cells)
Aetiology
- Can be:
- Sporadic (70%) - seen in adults (40s-50s)
- Medullary carcinoma associated with Multiple Endocrine Neoplasia Type 2a (MEN2a) can arise in very young patients
- MTC associated with phaeochromocytoma and hyperparathyroidism in these patients
- Consider prophlactic thyroidectomy as child
- Familial non-MEN seen in adults (40s-50s)
Genetic features
- Germline RET mutations
Pathophysiology
Morphology
- Sporadic cases - solitary nodule
- Familial cases - bilateral/multicentric
- C cell hyperplasia
- Composed of spindle or polygonal cells arranged in nests, trabeculae or follicles
- Associated amyloid deposition (abnormally folded calcitonin)
Prognostic factors
Good prognostic factors
- Young age, female
- Smaller tumour rise, confined to thyroid, no metastases
Negative prognostic factors
- Necrosis
- Many mitosis
- Squamous metaplasia
- Small cell morphology
- <50% cells calcitonin positive
- Type of RET mutation
- Some familial forms have more aggressive potential (MEN2B)
Clinical presentation
- Neck mass with local effects - dysphagia, hoearseness, airway compromise
- Paraneoplastic syndrome
- Diarrhoea - VIP production
- Cushings - ACTH production
Investigations
- Neck USS and FNA
- Measure serum base calcitonin
- 24 hour urinary metanephrines
- Further imaging to detect localised/advanced disease
- Check genetics for MEN
Management
Localised disease
- Total thyroidectomy - curative
- Local recurrence in 35% of patients
Advanced disease
- May involve tyrosine kinase inhibitors