Thyroid pathology in four patients with Cowden’s disease

Cowden’s disease (multiple hamartoma syndrome) is a rare genodermatosis, which carries an increased risk of malignancy, especially breast and thyroid carcinoma. Thyroid disease is the most common internal manifestation of the syndrome, but the histological features in benign cases have hitherto been...

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Veröffentlicht in:Pathology 2003-08, Vol.35 (4), p.311-314
1. Verfasser: Hemmings, Christine T.
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description Cowden’s disease (multiple hamartoma syndrome) is a rare genodermatosis, which carries an increased risk of malignancy, especially breast and thyroid carcinoma. Thyroid disease is the most common internal manifestation of the syndrome, but the histological features in benign cases have hitherto been relatively poorly described. Thyroidectomy specimens from four patients with Cowden’s disease have been reported in our laboratory in recent years. A number of rather distinctive features were common to all, raising the possibility of a distinctive ‘Cowden’s thyroid’ phenotype.
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subjects adenomatoid nodules
Cowden’s disease
Female
genodermatosis
Hamartoma Syndrome, Multiple - complications
Hamartoma Syndrome, Multiple - pathology
Humans
Male
multiple hamartoma syndrome
Pedigree
Siblings
Thyroid
Thyroid Gland - pathology
Thyroid Gland - surgery
Thyroid Nodule - etiology
Thyroid Nodule - pathology
Thyroid Nodule - surgery
title Thyroid pathology in four patients with Cowden’s disease
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