FV-PTC constitutes a frequently diagnosed subset of PTC, comprising roughly 32% of all PTC cases. β’ Although debate has surrounded the differences in the clinical courses and outcomes of patients with FV-PTC, our data suggest that the prognoses of patients with FV-PTC is basically similar to that o
Follicular variant of papillary thyroid carcinoma : A clinicopathologic study of a problematic entity
β Scribed by Jeffrey Liu; Bhuvanesh Singh; Giovanni Tallini; Diane L. Carlson; Nora Katabi; Ashok Shaha; R. Michael Tuttle; Ronald A. Ghossein
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 342 KB
- Volume
- 107
- Category
- Article
- ISSN
- 0008-543X
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
BACKGROUND
There is continuous debate regarding the optimal classification, prognosis, and treatment of the follicular variant of papillary thyroid carcinoma (FVPTC). The objective of this study was to assess the behavior of FVPTC, especially its encapsulated form, and shed more light on its true position in the classification scheme of well differentiated thyroid carcinoma.
METHODS
All patients with FVPTC, follicular thyroid adenoma (FTA), and follicular thyroid carcinoma (FTC) who were diagnosed between 1980 and 1995 were reviewed and reclassified according to the currently accepted definition of FVPTC. The tumors were separated into encapsulated and nonencapsulated (infiltrative/diffuse) types. Encapsulated tumors were subdivided further into tumors with or without capsular/vascular invasion. These different subtypes of FVPTC were correlated with outcome and with other clinicopathologic parameters.
RESULTS
After review by 4 pathologists, 78 patients were included in the study. Sixtyβone of 78 patients (78%) had encapsulated tumors (18 invasive, 43 noninvasive), and 17 patients had nonencapsulated tumors (infiltrative/diffuse). The gender distribution, age at presentation, and tumor size did not differ between patients with encapsulated and nonencapsulated FVPTC. Patients who had encapsulated FVPTC had a significantly lower rate of marked intratumor fibrosis (18%), extrathyroid extension (5%), and positive margins (2%) compared with patients who had nonencapsulated tumors (88%, 65%, and 50% respectively; P < .0001). Regional lymph node metastases were present in 14 of 78 patients (18%), and no patients had distant metastases. The lymph node metastatic rate was significantly higher in patients who had nonencapsulated tumors (11 of 17 patients; 65%) compared with patients who had encapsulated neoplasms (3 of 61 patients; 5%; P < .0001). In addition, lymph node metastases were not detected in any noninvasive, encapsulated FVPTCs. With a median followβup of 10.8 years, only 1 patient developed a recurrence, which occurred in an encapsulated FVPTC that had numerous invasive foci. None of the patients with noninvasive, encapsulated FVPTCs developed recurrences, including 31 patients who underwent lobectomy alone, with a median followβup of 11.1 years.
CONCLUSIONS
FVPTC appeared to be a heterogeneous disease composed of 2 distinct groups: an infiltrative/diffuse (nonencapsulated) subvariant, which resembles classic papillary carcinoma in its metastatic lymph node pattern and invasive growth, and an encapsulated form, which behaves more like FTA/FTC. Patients who had noninvasive, encapsulated FVPTCs did not develop lymph node metastases or recurrences and could be treated by lobectomy alone. If the current findings are confirmed, then strong consideration should be given to reclassifying encapsulated FVPTC as an entity that is close to the FTA/FTC class of tumors. Cancer 2006. Β© 2006 American Cancer Society.
π SIMILAR VOLUMES
## Abstract ## Objectives/Hypothesis: To determine the prevalence and extent of disease characteristics of the follicular variant of papillary thyroid carcinoma (FVβPTC) and the survival impact of this histopathological diagnosis compared to classical papillary thyroid carcinoma (CβPTC). ## Study
Crile and Hazard reported in 1953 a follicular pattern of papillary thyroid carcinoma. Little has been said about this pattern in the cytologic literature. From more than 8,000 thyroid aspirates in our files, we reviewed all those diagnosed as ''follicular variant of papillary carcinoma,'' ''suspect