Papillary carcinoma accounts for 80% of thyroid malignancies3. It is the most prevalent endocrine carcinoma.
Immunohistochemistry
cytokeratin |
positive1 |
9/92 |
|
high MW cytokeratin (LP34) |
5/92 |
8/84 |
|
0/84 |
|
4/92 |
|
7/92 |
|
positive1 (8/84) |
|
22/266, 20/205, 18/187 |
|
neuroendocrine markers |
negative1 |
negative3 |
|
positive1 (8/84) |
|
2/1410 |
|
4/92 |
Molecular genetics
There are three mutations commonly present in papillary carcinomas of the thyroid and each associated with specific features8:
BRAF mutations were associated with:
RET/PTC mutations:
Differential diagnosis
The follicular variant of papillary carcinoma: follicular adenoma and follicular carcinoma of the thyroid.
There is a solid variant of papillary carcinoma with a differential diagnosis which includes poorly differentiated carcinoma, medullary carcinoma, anaplastic carcinoma and metastatic carcinoma to the thyroid. It has a slightly worse prognosis than the classical papillary type but much better than poorly differentiated carcinoma. It has the same nuclear morphology and immunohistochemical profile as the classical papillary type.3
Management
Treatment is by thyroidectomy, radioiodine ablation of the thyroid remnants and TSH-suppressing doses of thyroxine.
Prognosis
With treatment, mortality is less than 10%.
References
1 Diagnostic histopathology of tumors. Edited by CDM Fletcher. 2nd edition. Churchill Livingstone. Pages 975-6.
This page last revised 30.1.2007.