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Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination
Neurofibromatosis-2 (NF2) is an autosomal-dominant disease, which is characterized by vestibular schwannomas (VSs) (acoustic neurinoma) as well as tumours of the peripheral and central nervous system, demonstrating a variety of expression. A 12-year-old girl presented to us with headache and ataxia...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Medknow Publications & Media Pvt Ltd
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379816/ https://www.ncbi.nlm.nih.gov/pubmed/28413544 http://dx.doi.org/10.4103/1793-5482.145347 |
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author | Kawsar, Khandkar Ali Haque, Md Raziul Chowdhury, Forhad Hossain |
author_facet | Kawsar, Khandkar Ali Haque, Md Raziul Chowdhury, Forhad Hossain |
author_sort | Kawsar, Khandkar Ali |
collection | PubMed |
description | Neurofibromatosis-2 (NF2) is an autosomal-dominant disease, which is characterized by vestibular schwannomas (VSs) (acoustic neurinoma) as well as tumours of the peripheral and central nervous system, demonstrating a variety of expression. A 12-year-old girl presented to us with headache and ataxia for four months. We examined and found a lump in the right side of her abdomen. On magnetic resonance imaging (MRI) of brain, a bilateral VS at the cerebellopontine (CP) angle was detected, and on computerized tomography (CT) scan and ultrasonography of her abdomen a large retroperitoneal schwannoma was revealed in the right side of her abdomen. At first, the right-sided CP angle tumour and two months later, the left-sided lesion was operated. After some days, she became mute and incontinent, and was found to have hydrocephalus on CT scan. We introduced a ventriculoperitoneal shunt. Then we operated the abdominal lump, which was histologically proven as schwannoma. The association of these three tumours is rare and untiring surgical approaches made her better. The patient recovered well except bilateral mild facial and vestibulocochlear deficit. |
format | Online Article Text |
id | pubmed-5379816 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53798162017-04-14 Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination Kawsar, Khandkar Ali Haque, Md Raziul Chowdhury, Forhad Hossain Asian J Neurosurg Case Report Neurofibromatosis-2 (NF2) is an autosomal-dominant disease, which is characterized by vestibular schwannomas (VSs) (acoustic neurinoma) as well as tumours of the peripheral and central nervous system, demonstrating a variety of expression. A 12-year-old girl presented to us with headache and ataxia for four months. We examined and found a lump in the right side of her abdomen. On magnetic resonance imaging (MRI) of brain, a bilateral VS at the cerebellopontine (CP) angle was detected, and on computerized tomography (CT) scan and ultrasonography of her abdomen a large retroperitoneal schwannoma was revealed in the right side of her abdomen. At first, the right-sided CP angle tumour and two months later, the left-sided lesion was operated. After some days, she became mute and incontinent, and was found to have hydrocephalus on CT scan. We introduced a ventriculoperitoneal shunt. Then we operated the abdominal lump, which was histologically proven as schwannoma. The association of these three tumours is rare and untiring surgical approaches made her better. The patient recovered well except bilateral mild facial and vestibulocochlear deficit. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5379816/ /pubmed/28413544 http://dx.doi.org/10.4103/1793-5482.145347 Text en Copyright: © 2014 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Case Report Kawsar, Khandkar Ali Haque, Md Raziul Chowdhury, Forhad Hossain Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination |
title | Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination |
title_full | Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination |
title_fullStr | Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination |
title_full_unstemmed | Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination |
title_short | Abdominal schwannoma in a case of neurofibromatosis type 2: A report of a rare combination |
title_sort | abdominal schwannoma in a case of neurofibromatosis type 2: a report of a rare combination |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5379816/ https://www.ncbi.nlm.nih.gov/pubmed/28413544 http://dx.doi.org/10.4103/1793-5482.145347 |
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