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Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review

BACKGROUND: Evaluation of palpable neck masses may be a diagnostic problem in pediatric patients, with differential diagnosis including congenital, inflammatory, tumoral and traumatic lesions. Ultrasonography is usually a satisfactory method to make a correct pre-operative evaluation of neck masses,...

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Autores principales: Catania, Vincenzo Davide, Manzoni, Carlo, Novello, Mariangela, Lauriola, Libero, Coli, Antonella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507769/
https://www.ncbi.nlm.nih.gov/pubmed/23130960
http://dx.doi.org/10.1186/1471-2431-12-172
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author Catania, Vincenzo Davide
Manzoni, Carlo
Novello, Mariangela
Lauriola, Libero
Coli, Antonella
author_facet Catania, Vincenzo Davide
Manzoni, Carlo
Novello, Mariangela
Lauriola, Libero
Coli, Antonella
author_sort Catania, Vincenzo Davide
collection PubMed
description BACKGROUND: Evaluation of palpable neck masses may be a diagnostic problem in pediatric patients, with differential diagnosis including congenital, inflammatory, tumoral and traumatic lesions. Ultrasonography is usually a satisfactory method to make a correct pre-operative evaluation of neck masses, although diagnosis is often challenging for the surgeon and the radiologist and sometimes only possible after a histopathological examination of the resected lesion. CASE PRESENTATION: We report an 8-month-old patient with a cervical, anterior midline mass. Ultrasonographic images showed features suggesting a partly cystic lesion, with a preoperative suspect of thyroglossal duct cyst. Histological examination, performed after surgical removal of the mass, led to a diagnosis of lymph node angiomyomatous hamartoma (AH). CONCLUSIONS: AH, a rarely occurring benign lymph node lesion, has been reported in the neck lateral region only twice. This case, presenting as a palpable neck midline mass, is the first reported case occurring in infancy. Although rare, AH should be included in the differential diagnosis of head and neck masses.
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spelling pubmed-35077692012-11-28 Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review Catania, Vincenzo Davide Manzoni, Carlo Novello, Mariangela Lauriola, Libero Coli, Antonella BMC Pediatr Case Report BACKGROUND: Evaluation of palpable neck masses may be a diagnostic problem in pediatric patients, with differential diagnosis including congenital, inflammatory, tumoral and traumatic lesions. Ultrasonography is usually a satisfactory method to make a correct pre-operative evaluation of neck masses, although diagnosis is often challenging for the surgeon and the radiologist and sometimes only possible after a histopathological examination of the resected lesion. CASE PRESENTATION: We report an 8-month-old patient with a cervical, anterior midline mass. Ultrasonographic images showed features suggesting a partly cystic lesion, with a preoperative suspect of thyroglossal duct cyst. Histological examination, performed after surgical removal of the mass, led to a diagnosis of lymph node angiomyomatous hamartoma (AH). CONCLUSIONS: AH, a rarely occurring benign lymph node lesion, has been reported in the neck lateral region only twice. This case, presenting as a palpable neck midline mass, is the first reported case occurring in infancy. Although rare, AH should be included in the differential diagnosis of head and neck masses. BioMed Central 2012-11-06 /pmc/articles/PMC3507769/ /pubmed/23130960 http://dx.doi.org/10.1186/1471-2431-12-172 Text en Copyright ©2012 Catania et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Catania, Vincenzo Davide
Manzoni, Carlo
Novello, Mariangela
Lauriola, Libero
Coli, Antonella
Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
title Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
title_full Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
title_fullStr Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
title_full_unstemmed Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
title_short Unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
title_sort unusual presentation of angiomyomatous hamartoma in an eight-month-old infant: case report and literature review
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507769/
https://www.ncbi.nlm.nih.gov/pubmed/23130960
http://dx.doi.org/10.1186/1471-2431-12-172
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