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Article

Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1.

Arquivos brasileiros de endocrinologia e metabologia - 1 Nov 2010

Fabbri Helena Campos, Mello Maricilda Palandi de, Soardi Fernanda Caroline, Esquiaveto-Aun Adriana Mangue, Oliveira Daniel Minutti de, Denardi Fernanda Canova, Moura-Neto Arnaldo, Garmes Heraldo Mendes, Baptista Maria Tereza Matias, Matos Patrícia Sabino de, Lemos-Marini Sofia Helena Valente de, D'Souza-Li Lilia Freire Rodrigues, Guerra-Júnior Gil

Abstract excerpt

Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary cancer syndrome characterized mostly by parathyroid, enteropancreatic, and anterior pituitary tumors. We present a case of an 8-year-old boy referred because of hypoglycemic attacks. His diagnosis was pancreatic insuli...

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Identifiers

PMID: 21340165
DOI: 10.1590/s0004-27302010000800016

Genes

MEN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21340165-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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Long-term follow-up of an 8-year-old boy with insulinoma as the first manifestation of a familial form of multiple endocrine neoplasia type 1.PMID 21340165Read ↗

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