Thyroid nodule classification: Difference between revisions
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* Granulomatous thyroiditis | * Granulomatous thyroiditis | ||
|0–3 % | |0–3 % | ||
|- | |||
|Nondiagnostic or Unsatisfactory | |||
| | |||
|1–4 % | |||
|- | |- | ||
|Follicular lesion of undetermined significance | |Follicular lesion of undetermined significance | ||
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* Microfollicular nodules | * Microfollicular nodules | ||
** Hurthle cell lesions | ** Hurthle cell lesions | ||
|15–30 % | |||
|- | |- | ||
|Suspicious for a follicular neoplasm | |Suspicious for a follicular neoplasm | ||
| | | | ||
* Suspicious for Hurthle cell neoplasm | * Suspicious for Hurthle cell neoplasm | ||
|60–75 % | |||
|- | |- | ||
|Malignant | |Malignant | ||
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|97–99 % | |97–99 % | ||
|} | |} | ||
==== Classification of neoplastic thyroid nodules based on their origin: ==== | ==== Classification of neoplastic thyroid nodules based on their origin: ==== | ||
{| class="wikitable" | {| class="wikitable" | ||
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|95% are sporadic tumors | |95% are sporadic tumors | ||
5% may be related to inherited genetics due to familial origin | 5% may be related to inherited genetics due to familial origin | ||
* Classic varient | |||
* tall cell variant | |||
* insular varient | |||
* columnar variant | |||
* Hürthle or oxyphilic variant | |||
* solid or trabecular variant | |||
* clear cell variant | |||
* diffuse sclerosing variant | |||
* cribriform morular variant | |||
* hobnail variant | |||
|- | |- | ||
|follicular (11%) | |follicular (11%) | ||
| | | | ||
* Benign follicular adenoma | |||
* Minimally invasive follicular carcinoma | |||
* Widely invasive follicular carcinoma | |||
* Encapsulated follicular variant of papillary thyroid cancer | |||
* Infiltrative variant of papillary thyroid cancer | |||
|- | |- | ||
|Hürthle cell (3%) | |Hürthle cell (3%) | ||
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|20% they are familial and occur as part of the multiple endocrine neoplasia (MEN) syndromes | |20% they are familial and occur as part of the multiple endocrine neoplasia (MEN) syndromes | ||
|} | |} | ||
Of the differentiated cancers, papillary cancer comprises about 85% of cases compared to about 10% that have follicular histology, and 3% that are Hu¨rthle cell or oxyphil tumors | |||
Neoplastic thyroid nodules subclassification: | |||
{| class="wikitable" | {| class="wikitable" | ||
! | ! | ||
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|- | |- | ||
| | | rowspan="2" |papillary thyroid cancer | ||
|Classic varient | |Classic varient | ||
| | | | ||
| | | | ||
|- | |- | ||
|tall cell variant | |tall cell variant | ||
|more aggressive tumor than classical papillary cancer | |more aggressive tumor than classical papillary cancer |
Revision as of 20:38, 11 August 2017
Thyroid nodule Microchapters |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mahshid Mir, M.D. [2]
Bethesda System for Reporting Thyroid Cytopathology
- 19888858
classification | FNA cytology | Predicted risk of malignancy |
---|---|---|
Benign |
|
0–3 % |
Nondiagnostic or Unsatisfactory | 1–4 % | |
Follicular lesion of undetermined significance |
|
5–15 % |
Atypia of undetermined significance |
| |
Follicular neoplasm |
|
15–30 % |
Suspicious for a follicular neoplasm |
|
60–75 % |
Malignant |
|
97–99 % |
Classification of neoplastic thyroid nodules based on their origin:
Origin | histologic subtypes | |||
---|---|---|---|---|
Nonmedullary thyroid cancers (NMTCs) | 95% of tumors | thyroid epithelial cells | papillary (85%) | 95% are sporadic tumors
5% may be related to inherited genetics due to familial origin
|
follicular (11%) |
| |||
Hürthle cell (3%) | ||||
anaplastic (1%) | ||||
Medullary thyroid cancers (MTCs) | 5% of all thyroid malignancies | calcitonin-producing parafollicular cells | 20% they are familial and occur as part of the multiple endocrine neoplasia (MEN) syndromes |
Of the differentiated cancers, papillary cancer comprises about 85% of cases compared to about 10% that have follicular histology, and 3% that are Hu¨rthle cell or oxyphil tumors
Neoplastic thyroid nodules subclassification:
Follicular thyroid lesions | Benign follicular adenoma | ||
Minimally invasive follicular carcinoma | |||
Widely invasive follicular carcinoma | |||
Encapsulated follicular variant of papillary thyroid cancer | |||
Infiltrative variant of papillary thyroid cancer | |||
papillary thyroid cancer | Classic varient | ||
tall cell variant | more aggressive tumor than classical papillary cancer
tumor cells with eosinophilic cytoplasm that are twice as tall as they are wide. The primary tumors tend to be large, they are often invasive, and many patients have both local and distant metastases at the time of diagnosis |
||
insular varient | solid nests of tumor, often separated by fibrous bands, but the tumor cell nuclei have the same characteristics as do the nuclei of classical papillary cancers. | ||
columnar variant | elongated cells with palisading nuclei. | ||
Hürthle or oxyphilic variant | Cellular features of Hürthle cell carcinomas but cells that are arranged in papillary formations. | ||
solid or trabecular variant | |||
clear cell variant | must be distinguished from clear cell carcinomas of other organs such as the kidney or colon that have metastasized to the thyroid. | ||
diffuse sclerosing variant | diffuse involvement of the thyroid, stromal fibrosis, and prominent lymphocytic infiltration | ||
cribriform morular variant | Prominent cribriform pattern with solid and spindle cell areas as well as squamous morules. This variant is often associated with familial adenomatous polyposis. | ||
hobnail variant | harbors BRAF V600E mutations and appears to be associated with a high risk of distant metastases and an increased disease-specific mortality |
Thyroid nodule classification based on the sonographhic features:
Classification system has been proposed by Horvath et al 3, with a modified recommendation from Jin Kwak et al 4.
TIRADS 1 | Normal thyroid gland | |||
TIRADS 2 | Benign lesions |
|
0% risk of malignancy | |
TIRADS 3 | Probably benign lesions |
|
<5% risk of malignancy | |
TIRADS 4 | 4a | One suspicious feature |
|
5-10% risk of malignancy |
4b | Two suspicious features | 10-80% risk of malignancy | ||
4c | Three/four suspicious features | |||
TIRADS 5 | All five suspicious features | Probably malignant lesions (more than 80% risk of malignancy) | >80% risk of malignancy | |
TIRADS 6 | Biopsy proven malignancy |
These categories are based on five suspicious sonographic features of malignancy:
Subclassificaton
- TIRADS 4a:
- TIRADS 4b:
- TIRADS 4c:
- TIRADS 5:
TIRADS 4a has , 4b and 4c may have TIRADS 5 category lesion have 3.