scholarly journals Clinicopathologic Features of Fatal Non-Anaplastic Follicular Cell–Derived Thyroid Carcinomas

Thyroid ◽  
2016 ◽  
Vol 26 (11) ◽  
pp. 1588-1597 ◽  
Author(s):  
Bin Xu ◽  
Tihana Ibrahimpasic ◽  
Laura Wang ◽  
Mona M. Sabra ◽  
Jocelyn C. Migliacci ◽  
...  
2014 ◽  
Author(s):  
Miguel Melo ◽  
Rocha Adriana Gaspar da ◽  
Joao Vinagre ◽  
Rui Batista ◽  
Joana Peixoto ◽  
...  

Author(s):  
Yun Yu ◽  
Adriana Krupa ◽  
Rebekah I. Keesler ◽  
Guy C. M. Grinwis ◽  
Mariska Ruijsscher ◽  
...  

2009 ◽  
Vol 133 (5) ◽  
pp. 683-691
Author(s):  
Ronald Ghossein

Abstract Context.—Despite past and recent efforts, many problems and controversies remain in the classification of thyroid carcinomas of follicular cell origin. These controversies have an impact on the prognosis and therapy of patients with thyroid carcinoma as well as on the development of robust cutting-edge research aimed at better outcome and quality of life. Objective.—To focus on 3 contentious areas with significant clinical value: the follicular variant of papillary thyroid carcinoma, the extent of invasion in follicular carcinoma, and the poorly differentiated thyroid carcinomas. Data Sources.—The published English language literature was reviewed. Conclusions.—Recent data show that prognosis and therapy for many disease entities can be better delineated if a meticulous microscopic examination is performed. An accurate assessment of the extent of invasion (especially vascular) is crucial. Proliferative grading (ie, mitosis and necrosis) is of high prognostic value and should be looked for in every specimen. In addition, molecular data gathered to date can help reassess these tumors at the histologic level. Classification proposals based on personal experience rather than adequate and careful clinical follow-up should be discouraged.


2012 ◽  
Vol 42 (1) ◽  
pp. 19-28 ◽  
Author(s):  
MÍRIAN ROMITTI ◽  
LUCIELI CEOLIN ◽  
DÉBORA RODRIGUES SIQUEIRA ◽  
CARLA VAZ FERREIRA ◽  
SIMONE MAGAGNIN WAJNER ◽  
...  

2014 ◽  
Vol 122 (7) ◽  
pp. 484-503 ◽  
Author(s):  
Ricardo R. Lastra ◽  
Virginia A. LiVolsi ◽  
Zubair W. Baloch

2020 ◽  
Vol 33 (12) ◽  
pp. 2458-2472 ◽  
Author(s):  
Ying-Hsia Chu ◽  
Lori J. Wirth ◽  
Alexander A. Farahani ◽  
Vânia Nosé ◽  
William C. Faquin ◽  
...  

Cancer ◽  
2007 ◽  
Vol 109 (10) ◽  
pp. 1965-1971 ◽  
Author(s):  
Lori A. Erickson ◽  
Long Jin ◽  
Nobuki Nakamura ◽  
Alina G. Bridges ◽  
Svetomir N. Markovic ◽  
...  

2005 ◽  
Vol 207 (4) ◽  
pp. 430-435 ◽  
Author(s):  
Sien-Yi Sheu ◽  
Rainer Görges ◽  
Christian Ensinger ◽  
Dietmar Öfner ◽  
Nadir R Farid ◽  
...  

2002 ◽  
Vol 126 (12) ◽  
pp. 1511-1514
Author(s):  
Weihua Tang ◽  
Kennichi Kakudo ◽  
Yasushi Nakamura ◽  
Misa Nakamura ◽  
Ichiro Mori ◽  
...  

Abstract Objective.—To describe the phenomenon of parathyroid gland involvement by thyroid carcinoma and to explore its clinicopathologic significance. Design.—We reviewed the clinicopathologic features and described the histopathologic characteristics of 20 cases of parathyroid involvement found in a series of 911 papillary thyroid carcinomas. Results.—Parathyroid involvement occurred in 3 patterns: (1) direct invasion from the main tumor with an infiltrative growth, (2) invasion of the parathyroid gland with an expansive growth and formation of a pseudocapsule between the carcinoma and the parathyroid gland, and (3) metastatic deposition within the parathyroid gland itself. Among the 20 cases, 6 (30%) had primary tumors measuring 1 cm or less, and 14 (70%) had primary tumors measuring more than 1 cm. The cases with smaller primary tumors had a comparatively lower rate of nodal metastasis (50% vs 100%, P = .02). Furthermore, none of the cases with smaller primary tumors had invasion of extrathyroid structures other than parathyroid gland, but such invasion was common among the cases with larger primary tumors (0% vs 71%, P = .01). Conclusion.—To the best of our knowledge, this is the first report showing that parathyroid involvement occurs in papillary thyroid carcinomas even in the early stage of the disease.


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