Medullary carcinoma thyroid – UG

Medullary carcinoma of thyroid
  • It is neuroendocrine neoplasm with C cell differentiation
  • Accounts for 5% to 10% of thyroid neoplasms
  • Tumor cells secrete calcitonin and increased levels of serum calcitonin is helpful for diagnosis and post operative follow up of patients
  • Other polypeptide hormones secreted by tumor cells are 
    • Serotonin
    • ACTH
    • Vasoactive intestinal polypeptide 
  • These tumros occur sporadically (in 70% cases) and in familial forms (30% of cases) with autosomal dominant inheritance. They occur in association with MEN syndrome (MEN 2A or 2B) or as familila tumors unassociated with MEN syndromes
  • Cytogenetics 
    •  Medullary carcinoma in MEN type 2 are associated with germline RET mutations that lead to constitutive activation of receptor
    • RET mutations are also present in one half of non-familial cases
  • Age –
    • Sporadic and familial –  occur in adulthood with peak incidence in 4th and 5th decade
    • Those associated with MEN type – occur in younger patients in the first decade of life 
  • Sex – Slight female predominance with female to male ratio of 1.3:1
  • Morphology 
    •  presents as unilateral solitary nodule in sporadic cases
    • Bilaterality and multicentricity is seen in familial cases
    • Gross –
      • Tumor is circumscribed, pale gray to tan with soft to firm in consistency
      • Areas of hemorrhage and necrosis are seen
    • Microscopy 
      • Tumor is composed of round, polygonal to spindle shaped cells, arranged in nests, lobular, trabecular and follicular pattern
      • Some tumors show anaplastic cells which are small and may predominate
      • Stroma shows acellular amyloid deposits derived from calcitonin polypeptides
      • Familial medullary carcinomas show multicentric C – cell hyperplasia in the adjacent thyroid parenchyma which is absent in sporadic cases. It is considered to be precursor lesion in familial cases
  • Electron microscopy 
    • reveals variable number of membranebound electron dense granules with in the cytoplasm of tumor cells
  • Clinical course 
    • presents as a mass in the neck.
    • sometimes associated with dysphagia and hoarsness
    • some of the cases may present with paraneoplastic syndrome due to secretion of hormones like VIP and ACTH
    • Calcitonin and Carcinoembryogenic antigen produced by tumor cells act as biomarkers
    • Medullary carcinomas arising in context of MEN 2B are more aggressive and metastasize more frequently than sporadic form 
    • Medullary carcinoma metastasizes to cervical lymph nodes and distant metastasis occurs to lungs, liver and bone
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  • Treatment and prognosis 
    • Treatment is total thyroidectomy
    • Prognosis for the younger patients (less than 40 Years ) is better than the elder patients
    • Prognosis in women is favourable than men

MICROPHOTOGRAPHS