Erschienen in:
01.10.2009 | Endocrine Tumors
Micromedullary Thyroid Cancer: How Micro Is Truly Micro?
verfasst von:
Venu G. Pillarisetty, MD, Steven C. Katz, MD, Ronald A. Ghossein, MD, R. Michael Tuttle, MD, Ashok R. Shaha, MD
Erschienen in:
Annals of Surgical Oncology
|
Ausgabe 10/2009
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Abstract
Background
The aggressive nature of medullary thyroid cancer (MTC) is evidenced by its propensity to present early with lymph node (LN) metastases. The clinical significance of sporadic MTC ≤1 cm (micro-MTC) is not clearly defined.
Methods
We performed a retrospective review of the clinical, laboratory, and pathologic data for all patients treated or followed at our institution for sporadic micro-MTC from 1987 through 2008.
Results
A total of 18 patients met the criteria for inclusion in our study. All tumors were unifocal and C-cell hyperplasia distant from the tumors was uniformly absent. Fourteen (78%) patients underwent total thyroidectomy, and the remaining four (22%) patients with tumors ≤0.5 cm had lobectomy with isthmusectomy alone. Four (22%) patients were found to have LN metastases. However, none of the nine patients with tumors <0.5 cm had clinical evidence of LN metastases. Patients were followed for a median of 3.3 (mean, 4.5) years, and there were no deaths. Postoperative calcitonin levels were available for all patients, of whom 14 had normal levels (range, 0–3.9 pg/ml). The four patients with elevated postoperative calcitonin levels (range, 6.3–644 pg/ml) had tumors ranging from 0.7–0.9 cm in size.
Conclusions
Tumors <0.5 cm were associated with a complete absence of clinically detectable nodal disease or elevated postoperative calcitonin levels. The complete absence of multifocal or bilateral disease argues against the need for completion thyroidectomy for sporadic micro-MTC.