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   <subfield code="a">Incidental Papillary Microcarcinoma of the Thyroid—Further Evidence of a Very Low Malignant Potential: A Retrospective Clinicopathological Study With Up to 30Years of Follow-Up</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Nikolaus Neuhold, Andrea Schultheis, Michael Hermann, Gabriela Krotla, Oskar Koperek, Peter Birner]</subfield>
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   <subfield code="a">Background: Despite the frequent occurrence of papillary microcarcinoma (PMC) of the thyroid, no consensus on its malignant potential or its treatment exists. The objective of this study was to analyze the clinicopathological characteristics of a retrospective cohort of consecutive patients with PMC treated in a single institution during a 30-year period and to study the incidence rates of PMC in all patients operated on for thyroid diseases during this period. Methods: Demographic data, clinical characteristics, histological workup of the resected glands, histopathological features, treatment, and follow-up data were studied. Results: Between 1975 and 1994, 759 PMCs were detected in 28,197 patients who received thyroidal surgery. The detection rate of PMC was significantly determined by the accuracy of the histological examination. Only 5 patients with PMC presented with clinically apparent lymph node metastases and 754 were incidental PMCs. Mean follow-up was 88±2 (range, 11-639) months. Only three patients experienced recurrence in cervical lymph nodes, all of whom presented with clinically suspect cervical nodes. No patient died of disease. Clinically apparent lymph node metastases and stage pT3 were significantly associated with recurrence. Conclusions: Incidentally detected PMC, even when multifocal, is a biologically indolent tumor that seldom if ever progresses. In contrast, clinically occult PMC detected due to clinically suspected and histological confirmed lymph node metastases or extrathyroidal growth may show a more aggressive course with disease recurrence and an eventual poorer prognosis.</subfield>
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   <subfield code="a">Society of Surgical Oncology, 2011</subfield>
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   <subfield code="a">Neuhold</subfield>
   <subfield code="D">Nikolaus</subfield>
   <subfield code="u">Department of Pathology and Bacteriology, Kaiserin-Elisabeth-Spital der Stadt Wien, Vienna, Austria</subfield>
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   <subfield code="a">Schultheis</subfield>
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   <subfield code="a">Hermann</subfield>
   <subfield code="D">Michael</subfield>
   <subfield code="u">Department of Surgery, Kaiserin-Elisabeth-Spital der Stadt Wien, Vienna, Austria</subfield>
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   <subfield code="a">Krotla</subfield>
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   <subfield code="u">Department of Nuclear Medicine, Kaiserin-Elisabeth-Spital der Stadt Wien, Vienna, Austria</subfield>
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   <subfield code="u">Clinical Institute of Pathology, Medical University of Vienna, Vienna, Austria</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
   <subfield code="d">Springer-Verlag</subfield>
   <subfield code="g">18/12(2011-11-01), 3430-3436</subfield>
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   <subfield code="D">1</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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