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  Vol. 114 No. 5, May 1988 TABLE OF CONTENTS
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Hürthle Cell Tumors of the Thyroid

A Flow Cytometric DNA Analysis

Adel K. El-Naggar, MD, PhD; John G. Batsakis, MD; Mario A. Luna, MD; Robert C. Hickey, MD

Arch Otolaryngol Head Neck Surg. 1988;114(5):520-521.


Abstract

• Twenty-five Hürthle cell tumors of the thyroid gland, histopathologically classified into three groups—adenomas, carcinomas, and indeterminant—have been studied by DNA flow cytometry using archived, paraffin-embedded tissues. Tumor ploidy characteristics were correlated with patient follow-up and survival with the conclusions that (1) nuclear DNA ploidy alone does not distinguish benign from malignant Hürthle cell tumors; (2) diploid DNA Hürthle cell carcinomas behave far less aggressively than aneuploid Hürthle cell carcinomas; and (3) all patients with aneuploid carcinomas died of their disease or are alive with persistent carcinoma.

(Arch Otolaryngol Head Neck Surg 1988;114:520-521)



Author Affiliations

From the Department of Anatomic Pathology, Division of Pathology (Drs El-Naggar, Batsakis, and Luna), and the Department of General Surgery, Division of Surgery (Dr Hickey), The University of Texas System Cancer Center, M. D. Anderson Hospital and Tumor Institute, Houston.


Footnotes

Accepted for publication Feb 8, 1988.

Reprint requests to Department of Pathology, The University of Texas System Cancer Center, M. D. Anderson Hospital and Tumor Institute, 1515 Holcombe Blvd, Houston, TX 77030 (Dr Batsakis).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Survival and Prognosis in Hurthle Cell Carcinoma of the Thyroid Gland
Bhattacharyya
Arch Otolaryngol Head Neck Surg 2003;129:207-210.
ABSTRACT | FULL TEXT  





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