Description

Medullary carcinoma of the thyroid may occur sporadically or in an hereditary form. It arises from the parafollicular C cells associated with calcitonin secretion. A variety of features have been found to be associated with prognosis.


 

Patients with the familial type of disease tend to have a better prognosis than those with the sporadic form.

 

Features associated with poor prognosis:

(1) extrathyroid tumor invasion, with extension into cervical soft tissue (patients with capsular invasion without extension into soft tissue have similar prognosis to those with intact capsule)

(2) age > 60 years

(3) distant metastases

(4) absence of amyloid in tumor

(5) aneuploid DNA pattern

(6) tumor diameter > 1 cm

(7) Stage III or IV at time of diagnosis

 

Features with a high risk of recurrence:

(1) absence of amyloid in tumor

(2) male sex

(3) extrathyroid tumor invasion

 

2 subgroups with 10 year survival comparable to general population

(1) Patients with hereditary form of medullary carcinoma detected by screening.

(2) Young patients with tumors < 1 cm in diameter and with clinical stage I or II at diagnosis.

 


To read more or access our algorithms and calculators, please log in or register.