Volume 65, Issue 2 pp. 137-140
Research Article
Full Access

Thyroid hemiagenesis

Ashok R. Shaha MD FACS

Corresponding Author

Ashok R. Shaha MD FACS

Head & Neck Service, Memorial Sloan-Kettering Cancer Center, New York, New York

Ashok R. Shaha, M.D., Head & Neck Service, 1275 York Avenue, New York, NY 10021. Telephone: (212) 639-7649; Fax: (212) 717-3302Search for more papers by this author
Rajesh Gujarati MD

Rajesh Gujarati MD

Head & Neck Service, Memorial Sloan-Kettering Cancer Center, New York, New York

Search for more papers by this author

Abstract

Background and Objectives

Thyroid hemiagenesis is a rare embryological condition, predominantly in females (3:1) with a left lobe being absent. The associated diseases in the remaining thyroid lobe include benign adenoma, multinodular goiter, hyperthyroidism, chronic thyroiditis, and rarely carcinoma. The most common pathology involved in thyroid hemiagenesis is hyperthyroidism. Presence of carcinoma in a patient with hemiagenesis is quite rare and very few cases are reported in the world literature.

Methods

We report a 30-year-old female who presented with left thyroid mass gradually increasing in size over a period of 3 months. The patient's pre-operative workup included a thyroid scan, which revealed a cold nodule in the left lobe with absent right lobe. A fine-needle aspiration biopsy was suspicious for papillary thyroid carcinoma. The patient underwent thyroid exploration and left thyroid lobectomy.

Results

The operative findings confirmed hemiagenesis of the right lobe and papillary carcinoma in the left lobe. All four parathyroids were in normal position.

Conclusions

The purpose of this presentation is to discuss and review the literature on thyroid hemiagenesis and present a rare case of absent right thyroid lobe with carcinoma in the remaining left thyroid lobe. J. Surg. Oncol. 1997;65:137–140. © 1997 Wiley-Liss, Inc.

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