A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma
Plexiform neurofibroma represents an uncommon variant of neurofibromatosis type 1, constituting only 5%–30% of all cases. Plexiform neurofibroma is usually diagnosed during childhood and arises from multiple nerves, manifesting as bulging and deforming masses that can also involve connective tissue...
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my.ums.eprints.352342023-03-23T02:13:17Z https://eprints.ums.edu.my/id/eprint/35234/ A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma Siti Sarah Mohd Ramli Goh, Bee See Faizah Mohd Zaki Suria Hayati Md Pauzi Mohd Fariz Amri RC254-282 Neoplasms. Tumors. Oncology Including cancer and carcinogens RJ370-550 Diseases of children and adolescents Plexiform neurofibroma represents an uncommon variant of neurofibromatosis type 1, constituting only 5%–30% of all cases. Plexiform neurofibroma is usually diagnosed during childhood and arises from multiple nerves, manifesting as bulging and deforming masses that can also involve connective tissue and skin folds. We report a case of a two-year-old girl who presented with worsening stridor since birth and later exhibited progressively increasing left neck swelling at the age of 10 months old. Ultrasound and magnetic resonance imaging (MRI) showed a lobulated solid mass in the left deep neck space extending to the midline and having a mass effect on the airway with involvement of the supraglottic region. Tracheostomy was done, and a biopsy of the supraglottic lesion revealed a plexiform neurofibroma. The patient was conservatively managed after a discussion with her parents concerning the associated potential of operative morbidity. The patient’s parents had learned about tracheostomy care, and the patient was scheduled for yearly MRI surveillance. MRI was performed again three months after the initial diagnosis and showed stable lesion. Plexiform neurofibroma is a slow-growing tumor. A treatment decision must consider the benefits of surgery and the morbidity of the progressing disease. Hence, airway management is crucial prior to the final decision of such cases Galenos Publishing House 2021 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/35234/1/Abstract.pdf text en https://eprints.ums.edu.my/id/eprint/35234/2/Full%20text.pdf Siti Sarah Mohd Ramli and Goh, Bee See and Faizah Mohd Zaki and Suria Hayati Md Pauzi and Mohd Fariz Amri (2021) A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma. Turkish Archives of Otorhinolaryngology, 59. pp. 297-301. ISSN 2667-7474 https://cms.galenos.com.tr/Uploads/Article_50940/tao-59-297-En.pdf https://doi.org/10.4274/tao.2021.2021-3-10 |
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RC254-282 Neoplasms. Tumors. Oncology Including cancer and carcinogens RJ370-550 Diseases of children and adolescents Siti Sarah Mohd Ramli Goh, Bee See Faizah Mohd Zaki Suria Hayati Md Pauzi Mohd Fariz Amri A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma |
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Plexiform neurofibroma represents an uncommon variant of neurofibromatosis type 1, constituting only 5%–30% of all cases. Plexiform neurofibroma is usually diagnosed during childhood and arises from multiple nerves, manifesting as bulging and deforming masses that can also involve connective tissue and skin folds. We report a case of a two-year-old girl who presented with worsening stridor since birth and later exhibited progressively increasing left neck swelling at the age of 10 months old. Ultrasound and magnetic resonance imaging (MRI) showed a lobulated solid mass in the left deep neck space extending to the midline and having a mass effect on the airway with involvement of the supraglottic region. Tracheostomy was done, and a biopsy of the supraglottic lesion revealed a plexiform neurofibroma. The patient was conservatively managed after a discussion with her parents concerning the associated potential of operative morbidity. The patient’s parents had learned about tracheostomy care, and the patient was scheduled for yearly MRI surveillance. MRI was performed again three months after the initial diagnosis and showed stable lesion. Plexiform neurofibroma is a slow-growing tumor. A treatment decision must consider the benefits of surgery and the morbidity of the progressing disease. Hence, airway management is crucial prior to the final decision of such cases |
format |
Article |
author |
Siti Sarah Mohd Ramli Goh, Bee See Faizah Mohd Zaki Suria Hayati Md Pauzi Mohd Fariz Amri |
author_facet |
Siti Sarah Mohd Ramli Goh, Bee See Faizah Mohd Zaki Suria Hayati Md Pauzi Mohd Fariz Amri |
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Siti Sarah Mohd Ramli |
title |
A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma |
title_short |
A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma |
title_full |
A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma |
title_fullStr |
A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma |
title_full_unstemmed |
A Rare Tumor in the Neck of a Child: Plexiform Neurofibroma |
title_sort |
rare tumor in the neck of a child: plexiform neurofibroma |
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Galenos Publishing House |
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2021 |
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https://eprints.ums.edu.my/id/eprint/35234/1/Abstract.pdf https://eprints.ums.edu.my/id/eprint/35234/2/Full%20text.pdf https://eprints.ums.edu.my/id/eprint/35234/ https://cms.galenos.com.tr/Uploads/Article_50940/tao-59-297-En.pdf https://doi.org/10.4274/tao.2021.2021-3-10 |
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