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Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma

Hypothalamic hamartomas are rare tumors that are most often diagnosed in early childhood. These lesions are classified as giant hypothalamic hamartomas when they exceed 4 cm in any 1 dimension. The most common presenting symptoms associated with these lesions are precocious puberty, gelastic seizure...

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Detalles Bibliográficos
Autores principales: Cristobal, Alberto, Vorona, Gregory, Ritter, Ann, Lanni, Susan, Urbine, Jacqueline
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303913/
https://www.ncbi.nlm.nih.gov/pubmed/32577141
http://dx.doi.org/10.1016/j.radcr.2020.05.041
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author Cristobal, Alberto
Vorona, Gregory
Ritter, Ann
Lanni, Susan
Urbine, Jacqueline
author_facet Cristobal, Alberto
Vorona, Gregory
Ritter, Ann
Lanni, Susan
Urbine, Jacqueline
author_sort Cristobal, Alberto
collection PubMed
description Hypothalamic hamartomas are rare tumors that are most often diagnosed in early childhood. These lesions are classified as giant hypothalamic hamartomas when they exceed 4 cm in any 1 dimension. The most common presenting symptoms associated with these lesions are precocious puberty, gelastic seizures, and (less commonly) syndromic conditions such as Pallister-Hall syndrome. We present a unique case of an asymptomatic giant hypothalamic hamartoma diagnosed prenatally by fetal magnetic resonance imaging and followed throughout infancy. This case demonstrates the utility of multimetric analysis using difference sequences, including diffuse-weighted imaging, to assess specific properties of intracranial lesions detected in utero and to aid in accurate diagnosis prior to birth.
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spelling pubmed-73039132020-06-22 Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma Cristobal, Alberto Vorona, Gregory Ritter, Ann Lanni, Susan Urbine, Jacqueline Radiol Case Rep Neuroradiology Hypothalamic hamartomas are rare tumors that are most often diagnosed in early childhood. These lesions are classified as giant hypothalamic hamartomas when they exceed 4 cm in any 1 dimension. The most common presenting symptoms associated with these lesions are precocious puberty, gelastic seizures, and (less commonly) syndromic conditions such as Pallister-Hall syndrome. We present a unique case of an asymptomatic giant hypothalamic hamartoma diagnosed prenatally by fetal magnetic resonance imaging and followed throughout infancy. This case demonstrates the utility of multimetric analysis using difference sequences, including diffuse-weighted imaging, to assess specific properties of intracranial lesions detected in utero and to aid in accurate diagnosis prior to birth. Elsevier 2020-06-16 /pmc/articles/PMC7303913/ /pubmed/32577141 http://dx.doi.org/10.1016/j.radcr.2020.05.041 Text en © 2020 The Authors. Published by Elsevier Inc. on behalf of University of Washington. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Neuroradiology
Cristobal, Alberto
Vorona, Gregory
Ritter, Ann
Lanni, Susan
Urbine, Jacqueline
Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma
title Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma
title_full Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma
title_fullStr Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma
title_full_unstemmed Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma
title_short Pre- and postnatal MR imaging of an asymptomatic giant hypothalamic hamartoma
title_sort pre- and postnatal mr imaging of an asymptomatic giant hypothalamic hamartoma
topic Neuroradiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7303913/
https://www.ncbi.nlm.nih.gov/pubmed/32577141
http://dx.doi.org/10.1016/j.radcr.2020.05.041
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