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An Orthotopic Mouse Model of Anaplastic Thyroid Carcinoma
Published on: April 17, 2013
Poorly differentiated thyroid carcinoma: a cytologic-histologic review.
Massimo Bongiovanni1, Peter M Sadow, William C Faquin
1Pathologie Clinique, Hôpitaux Universitaires de Genève, Geneva, Switzerland.
Advances in Anatomic Pathology
|August 25, 2009
Summary
Poorly differentiated thyroid carcinoma (PDTC) is a distinct entity recognized by the WHO, with specific histologic and cytologic diagnostic criteria. Aggressive management including surgery and radioactive iodine is recommended for PDTC.
Area of Science:
- Endocrinology
- Pathology
- Oncology
Background:
- Poorly differentiated thyroid carcinoma (PDTC) was recognized as a distinct entity in the 2004 WHO classification of endocrine tumors.
- Specific diagnostic criteria were refined in 2006 by expert thyroid pathologists.
Purpose of the Study:
- To detail the histologic and cytologic features for diagnosing PDTC.
- To highlight key diagnostic markers and molecular findings.
- To outline current management strategies for PDTC.
Main Methods:
- Review of histologic and cytologic features of PDTC.
- Analysis of immunohistochemical markers (thyroglobulin, TTF-1, p53).
- Examination of molecular findings, focusing on ras mutations.
Main Results:
- Histologic criteria include insular, solid, or trabecular architecture with specific nuclear or mitotic features, or necrosis.
- Cytologic findings suggestive of PDTC include specific patterns, high N/C ratio, and crowding.
- Most PDTCs are thyroglobulin and TTF-1 positive; ras mutations are common.
Conclusions:
- PDTC diagnosis relies on specific histologic and cytologic features.
- Immunohistochemistry and molecular analysis aid in diagnosis and understanding.
- Aggressive treatment involving surgery, radioactive iodine, and potentially radiotherapy is indicated.
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