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Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant

Galactocele is a benign breast lesion, usually occurring in nursing women. This lesion is a rare cause of breast enlargement in children. In this paper we describe the case of an infant with hyperprolactinemia (which persisted throughout 15 years of clinical observation) and bilateral galactocele. W...

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Autores principales: Tomasi, Paolo A., Fanciulli, Giuseppe, Casti, Tiziana, Delitala, Giuseppe
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778792/
https://www.ncbi.nlm.nih.gov/pubmed/19956638
http://dx.doi.org/10.1155/2009/578610
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author Tomasi, Paolo A.
Fanciulli, Giuseppe
Casti, Tiziana
Delitala, Giuseppe
author_facet Tomasi, Paolo A.
Fanciulli, Giuseppe
Casti, Tiziana
Delitala, Giuseppe
author_sort Tomasi, Paolo A.
collection PubMed
description Galactocele is a benign breast lesion, usually occurring in nursing women. This lesion is a rare cause of breast enlargement in children. In this paper we describe the case of an infant with hyperprolactinemia (which persisted throughout 15 years of clinical observation) and bilateral galactocele. We speculate that a congenital midline defect in our patient might have impaired the normal dopaminergic inhibitory tone on pituitary lactotroph cells, thus leading to an increased prolactin secretion by the pituitary gland; this, in turn, might have favored the development of the galactocele.
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spelling pubmed-27787922009-12-02 Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant Tomasi, Paolo A. Fanciulli, Giuseppe Casti, Tiziana Delitala, Giuseppe Int J Pediatr Endocrinol Case Report Galactocele is a benign breast lesion, usually occurring in nursing women. This lesion is a rare cause of breast enlargement in children. In this paper we describe the case of an infant with hyperprolactinemia (which persisted throughout 15 years of clinical observation) and bilateral galactocele. We speculate that a congenital midline defect in our patient might have impaired the normal dopaminergic inhibitory tone on pituitary lactotroph cells, thus leading to an increased prolactin secretion by the pituitary gland; this, in turn, might have favored the development of the galactocele. Hindawi Publishing Corporation 2009 2009-02-26 /pmc/articles/PMC2778792/ /pubmed/19956638 http://dx.doi.org/10.1155/2009/578610 Text en Copyright © 2009 Paolo A. Tomasi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Tomasi, Paolo A.
Fanciulli, Giuseppe
Casti, Tiziana
Delitala, Giuseppe
Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant
title Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant
title_full Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant
title_fullStr Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant
title_full_unstemmed Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant
title_short Persistent Hyperprolactinemia and Bilateral Galactocele in a Male Infant
title_sort persistent hyperprolactinemia and bilateral galactocele in a male infant
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778792/
https://www.ncbi.nlm.nih.gov/pubmed/19956638
http://dx.doi.org/10.1155/2009/578610
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