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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,...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3507769 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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