Plexiform Neurofibroma of the Larynx in Children: About an Unusual Case Report
<p><strong>Introduction: </strong>The plexiform neurofibroma is a rare benign tumor which is often associated to type 1 neurofibromatosis or Von Recklinghausen's disease. The laryngeal involvement in neurofibromatosis is extremely rare. </p><p>The objective of our...
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Archives of Otolaryngology and Rhinology - Peertechz Publications,
2016-07-04.
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LEADER | 00000 am a22000003u 4500 | ||
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001 | peertech__10_17352_2455-1759_000020 | ||
042 | |a dc | ||
100 | 1 | 0 | |a R Mahdoufi |e author |
700 | 1 | 0 | |a I Barhmi |e author |
700 | 1 | 0 | |a N Tazi |e author |
700 | 1 | 0 | |a R Sami |e author |
700 | 1 | 0 | |a R Abada |e author |
700 | 1 | 0 | |a M Roubal |e author |
700 | 1 | 0 | |a M Mahtar |e author |
245 | 0 | 0 | |a Plexiform Neurofibroma of the Larynx in Children: About an Unusual Case Report |
260 | |b Archives of Otolaryngology and Rhinology - Peertechz Publications, |c 2016-07-04. | ||
520 | |a <p><strong>Introduction: </strong>The plexiform neurofibroma is a rare benign tumor which is often associated to type 1 neurofibromatosis or Von Recklinghausen's disease. The laryngeal involvement in neurofibromatosis is extremely rare. </p><p>The objective of our report is the consideration of laryngeal neurofibromatosis in the differential diagnosis of dyspnea in infants and children. </p><p><strong>Summary of the clinical case:</strong> We report the case of a 4 year-old child who presented with inspiratory dyspnea. Laryngoscopy revealed a mass obstructing completely the laryngeal vestibule. Pathological examination of the resected tissue revealed a plexiform neurofibroma after immunohistochemical examination. The patient had regular follow up and she remained symptom free. </p><p><strong>Discussion: </strong>There is an association between neurofibromatosis type 1 and plexiform neurofibromas of the larynx. Analysis of the margins of neurofibromas of the larynx associated with neurofibromatosis type 1 may elp predict clinical behavior.</p> | ||
540 | |a Copyright © R Mahdoufi et al. | ||
546 | |a en | ||
655 | 7 | |a Case Report |2 local | |
856 | 4 | 1 | |u https://doi.org/10.17352/2455-1759.000020 |z Connect to this object online. |