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Vol. 13. Núm. 1.
Páginas 49-60 (enero 2009)
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Vol. 13. Núm. 1.
Páginas 49-60 (enero 2009)
Acceso a texto completo
Nesidioblastosis del adulto coexistente con insulinoma
Adult Nesidioblastosis Concurrent with Insulinoma
Visitas
8513
Katherine Restrepo1,
Autor para correspondencia
kareser@gmail.com
tne@tumoresneuroendocrinos.org

Correspondencia Instituto Nacional de Cancerología. Av. 1a No. 9–85. Bogotá, Colombia. Tel.:éfono: 334 1111.
, Gloria Garavito1, Leonardo Rojas1, Alfredo Romero1,2, Fabián Neira1,2, Ricardo Oliveros1,2, Nadin Abisambra1,2
1 Instituto Nacional de Cancerología, Bogotá, Colombia
2 Universidad Nacional de Colombia, Bogotá, Colombia
Este artículo ha recibido
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Resumen

La nesidioblastosis es poco común, pero ampliamente reconocida como causa de la hipoglucemia hiperinsulinémica persistente de la infancia. En adultos, el insulinoma es la principal causa de hipoglucemia hiperinsulinémica, pero también se han identificado casos de nesidioblastosis, los cuales se denominan ‘síndrome de hipoglucemia pancreatógena no insulinoma’. Los primeros casos de nesidioblastosis del adulto que fueron descritos se asociaron con otras condiciones, como insulinoma y tumores neuroendocrinos pancreáticos y MEN-1. En este artículo se describe un caso de nesidioblastosis coexistente con insulinoma en una paciente de 20 años; se hace una revisión de la literatura; se plantea la discusión sobre su posible etiología, presentación clínica, diagnóstico, tratamiento y, finalmente, se presenta un algoritmo para su estudio.

Palabras clave:
Hipoglucemia
hiperinsulinismo
nesidioblastosis
insulinoma
adulto
Abstract

Nesidioblastosis is infrequent; however, it is widely recognized as the cause of persistent infant hyperinsulinemic hypoglycemia. Among adults, insulinoma is the major cause of hyperinsulinemia hypoglycemia, but identification has also been made of cases of nesidioblastosis which are designated as ‘non insulinoma pancreatogena hypoglycemic syndrome’. The first case descriptions of adult nesidioblastosis were associated with other conditions such as insulinoma and neuroenodocrinal pancreatic tumors, and MEN-1. This article describes a case of nesidioblastosis concurrent with insulinoma in a 20-year old patient; the literature is reviewed; discussion is provided on possible etiology, clinical manifestation, diagnosis, treatment, and a concluding algorithm.

Key words:
Hypoglycemia
hyperinsulinism
nessidioblastosis
insulinoma
adult
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