Resumen

YANES QUESADA, Marelys et al. Atypical multiple endocrine neoplasia: A case presentation. Rev Cubana Endocrinol [online]. 2007, vol.18, n.1. ISSN 1561-2953.

Multiple endocrine neoplasm are syndromes with autosomal dominant inheritance, where there is tumoral involvement of two or more endoce glands, grouped by glandular afection as: 1, 2A, 2B, and mixed. Case of a female patient, aged 44 seen in National Institute of Endocrinology (NIEN) and that when she aged 24 was operted on by a carcinoid bronchial adenoma, eleven year after she showed a increase in hands and feets volumen and is admissed in our service and is diagnosed as HG-producer hypophyseal adenoma, a tumor of pineal gland as well as a chromaffin tumor in right kidney. Due to atypical picture, and the lack of similar cases in reviewed literature, we considered appropriate its presentation.

Palabras clave : Multiple endocrine neoplasia.