Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature
We describe the case of a nine-month-old patient with a nasopharyngeal choristoma. The case presented includes the retrospective review of the historical, radiological, surgical and histological assessment of this pathology as well as a literature review of this entity. This case was presented in an...
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KeAi Communications Co., Ltd.
2021
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oai:doaj.org-article:5d4b8c3bf9b74109932d3a3f1af1704d2021-12-02T17:29:50ZNasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature2095-881110.1016/j.wjorl.2020.02.001https://doaj.org/article/5d4b8c3bf9b74109932d3a3f1af1704d2021-10-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2095881120300159https://doaj.org/toc/2095-8811We describe the case of a nine-month-old patient with a nasopharyngeal choristoma. The case presented includes the retrospective review of the historical, radiological, surgical and histological assessment of this pathology as well as a literature review of this entity. This case was presented in an infant with difficulty feeding, nasal obstruction and failure to thrive, evaluated with flexible nasal endoscopy, CT and MRI. The lesion was then surgically removed without complications. Nasopharyngeal choristoma is a rare congenital non-malignant mass, which may present within a range of symptoms and severity according to its size, growth and location.Maria Monica Baquero-HoyosJosé Antonio MarinoJosé Luis MayorgaKeAi Communications Co., Ltd.articleChoristomaNeuroglial heterotopyNasopharynxOtorhinolaryngologyRF1-547SurgeryRD1-811ENWorld Journal of Otorhinolaryngology-Head and Neck Surgery, Vol 7, Iss 4, Pp 318-321 (2021) |
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Choristoma Neuroglial heterotopy Nasopharynx Otorhinolaryngology RF1-547 Surgery RD1-811 |
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Choristoma Neuroglial heterotopy Nasopharynx Otorhinolaryngology RF1-547 Surgery RD1-811 Maria Monica Baquero-Hoyos José Antonio Marino José Luis Mayorga Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature |
description |
We describe the case of a nine-month-old patient with a nasopharyngeal choristoma. The case presented includes the retrospective review of the historical, radiological, surgical and histological assessment of this pathology as well as a literature review of this entity. This case was presented in an infant with difficulty feeding, nasal obstruction and failure to thrive, evaluated with flexible nasal endoscopy, CT and MRI. The lesion was then surgically removed without complications. Nasopharyngeal choristoma is a rare congenital non-malignant mass, which may present within a range of symptoms and severity according to its size, growth and location. |
format |
article |
author |
Maria Monica Baquero-Hoyos José Antonio Marino José Luis Mayorga |
author_facet |
Maria Monica Baquero-Hoyos José Antonio Marino José Luis Mayorga |
author_sort |
Maria Monica Baquero-Hoyos |
title |
Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature |
title_short |
Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature |
title_full |
Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature |
title_fullStr |
Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature |
title_full_unstemmed |
Nasopharyngeal neuroglial heterotopy - Choristoma: Case report and review of the literature |
title_sort |
nasopharyngeal neuroglial heterotopy - choristoma: case report and review of the literature |
publisher |
KeAi Communications Co., Ltd. |
publishDate |
2021 |
url |
https://doaj.org/article/5d4b8c3bf9b74109932d3a3f1af1704d |
work_keys_str_mv |
AT mariamonicabaquerohoyos nasopharyngealneuroglialheterotopychoristomacasereportandreviewoftheliterature AT joseantoniomarino nasopharyngealneuroglialheterotopychoristomacasereportandreviewoftheliterature AT joseluismayorga nasopharyngealneuroglialheterotopychoristomacasereportandreviewoftheliterature |
_version_ |
1718380730542718976 |