2016, Number 3
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Rev Méd Electrón 2016; 38 (3)
Cowden syndrome. Presentation of an infrequent case
Arredondo BA, Huerta RJ, Domínguez CT, Pérez ZJ
Language: Spanish
References: 13
Page: 424-430
PDF size: 460.37 Kb.
ABSTRACT
Cowden syndrome is an inherited disease, of dominant auto somatic transmission,
characterized by the presence of multiple hamartomas and nodules in skin and oral
mucosa, together with anomalies in breasts and thyroids, and polyps in the
gastrointestinal tract; they tend to become malignant, above all in breast and
thyroids. The precocious diagnosis after finding skin lesions and digestive disturbances should redirect the study, looking for malignancy in thyroids and, in
cases of women patients, in breast. We presented a clinical case debuting with
digestive disturbances interpreted as upper digestive bleeding. During the
endoscopy, several duodenal polyps were observed that together with skin
disturbances led to the diagnosis. The presence of skin facial papules and the oral
mucosa papillomatosis are the bigger clinical criteria to stablish the Cowden
syndrome diagnosis; they should raise the clinician alert toward the possibility of
other neoplastic lesions, sometimes hidden, especially in the breast, thyroids and
alimentary canal, with malignant character.
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