2012
DOI: 10.1007/s12070-011-0475-4
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Schwannoma of the Cervical Vagus Nerve in a Child: A Case Report

Abstract: Schwannoma are relatively rare tumor and even rarer in children. Nerve sheath tumors arising from the cervical nerve are extremely rare. We report a 13-year old boy presented with a history of an asymptomatic right cervical swelling since one year. An ultrasound and FNAC revealed schwannoma. He was meticulously evaluated with MRI. Surgical excision of the lesion was carried out and histopathological examination confirmed the diagnosis. Patient recovered completely without any morbidity. We are presenting this … Show more

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Cited by 7 publications
(5 citation statements)
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“…Neurogenic tumors make up only 2% of benign, pediatric neoplasms but they are commonly associated with underlying conditions such as neurofibromatosis types one and two (NF-1, NF-2) [ 3 , 6 ]. Schwannomas in particular are characteristic of NF-2, and while bilateral vestibular schwannomas are the hallmark of the disease, schwannomas of other peripheral nerves may arise and warrant further testing.…”
Section: Discussionmentioning
confidence: 99%
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“…Neurogenic tumors make up only 2% of benign, pediatric neoplasms but they are commonly associated with underlying conditions such as neurofibromatosis types one and two (NF-1, NF-2) [ 3 , 6 ]. Schwannomas in particular are characteristic of NF-2, and while bilateral vestibular schwannomas are the hallmark of the disease, schwannomas of other peripheral nerves may arise and warrant further testing.…”
Section: Discussionmentioning
confidence: 99%
“…These rare lesions can arise from peripheral nerves surrounded by Schwann cells in any area of the body. They are most often found in the head, neck, and extremities [1][2][3]. The vast majority of schwannomas occur in adults, with fewer than 10% diagnosed in patients younger than 21 years [1][2][3].…”
Section: Introductionmentioning
confidence: 99%
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“…Their origin site is usually the mediastinum [6]. Typically they are slow growing, homogeneous and mostly benign tumors, which rarely occur in the gastrointestinal (GI) tract, representing about 2–6% of all mesenchymal tumors [7]. The most common site of all GI cases is the stomach, followed by the colon and rectum.…”
Section: Discussionmentioning
confidence: 99%
“…Some of these tumors are present as a part of the NF2 type genetic syndrome, especially at bilateral occurrence. From cranial nerves, this tumor mostly affects VIII cranial nerve and is called vestibular schwannoma or acoustic neurinoma [86]. Vestibular schwannomas can cause loss of hearing and tinnitus.…”
Section: Other Pediatric Cns Tumorsmentioning
confidence: 99%