Case Reports in Medicine

Case Reports in Medicine / 2016 / Article

Case Report | Open Access

Volume 2016 |Article ID 2786030 |

Xiao-Hui Ma, Hai-Chun Zhou, Can Lai, Kun Zhu, Xuan Jia, "Pediatric Isolated Sinonasal Schwannoma: A New Case Report and Literature Review", Case Reports in Medicine, vol. 2016, Article ID 2786030, 3 pages, 2016.

Pediatric Isolated Sinonasal Schwannoma: A New Case Report and Literature Review

Academic Editor: Lothar Bergmann
Received30 Jun 2016
Revised09 Oct 2016
Accepted12 Oct 2016
Published02 Nov 2016


Schwannomas of the paranasal sinus are uncommon. Less than 4% of schwannomas involve the nasal cavity and paranasal sinuses, even less in the pediatric age group. A case of schwannoma arising in maxillary sinus in a 2.5-year-old Chinese boy is reported. The basis for discussion of this case is the exceptional rarity of sinonasal schwannoma in pediatric patients.

1. Introduction

Schwannomas are neoplasms that originate from Schwann cells of the neural sheath, most of which are benign and well encapsulated occurring in middle-aged adults, between the ages of 40 and 60, with an equal gender distribution [1]. Schwannomas are particularly rare in kids—merely 0.7 percent of all schwannomas took place in children during their first decade of life [2]. Computed tomography (CT) shows usually a round homogeneous density lesion, without calcification generally [3]. The cases are of interest due to the unusual arising region, uncommon pediatric patient, and the relative rarity of the radiological findings.

2. Case Report

A 2.5-year-old boy presented with a half-year history of nasal obstruction, rhinorrhea. There was no history of pain, fever, or trauma. Nasal stuffiness was aggravated gradually, in particular the right nasal passage, with nocturnal snoring and mouth breathing and without suffocation, headache, coma, and convulsions. Eyes secretions increased during the last 3 months, with frequent tears. The boy had a normal appetite, stool, and urine and did not have significant weight loss since the onset. A smooth surface bright red mass could be seen in the forepart of right nasal cavity with considerable purulent secretions in bilateral nasal cavity and without exophthalmos and lymphadenectasis. Bilateral external auditory canals were unobstructed, without fluid inside, and both had tympanic membrane integrity, though depression was observed in the right side. The rest of the patient’s physical examinations were normal, without pigmentary changes of the skin or any other signs or symptoms of neurofibromatosis (NF); there was no family history as well.

Unenhanced CT images revealed a round (diameter = 42 mm) expansive soft-tissue mass with stellate-shaped calcification which originated from the right maxillary sinus, invaded into ethmoid sinus, sphenoid sinus region, and forepart of the right nasopharynx and oropharynx, and prolapsed into ipsilateral nasal cavity, pressuring and remodeling the adjacent bony wall of maxilla, nasal septum, and sphenoid bone with most bony margins preserved and without teeth being involved (Figure 1). The postcontrast axial CT scan showed marked heterogeneous enhancement (Figure 2)—significant enhancement (104 HU) surrounding the calcification except posterior and left part (42 HU) of the tumor, nowhere without enhancement—compared to the CT scan without contrast agent (32–50 HU).

3. Discussion

Schwannomas may develop virtually in all parts of the body, while the head and neck region is the most common site of origin accounting for 25% to 45% of benign schwannomas [4]. Sinonasal region, even though it is located in the head, has an extremely low incidence (about 4%) of schwannomas [5, 6] and an even lower incidence when referring to pediatric patients [2].

Schwannomas develop from any peripheral, cranial, or any autonomic nerve that has a Schwann sheath. It has been postulated that sinonasal schwannomas arise from Schwann cells of the ophthalmic and maxillary branches of the trigeminal nerve or from autonomic nerves to the septal vessels and mucosa [5, 7].

Schwannomas are usually benign neoplasms that could take place in individuals with neurofibromatosis type 2 (NF2), a kind of autosomal-dominant inherited tumor predisposition syndrome induced by NF2 gene mutations located in chromosome 22, hallmark tumor of which is the vestibular schwannoma occurring bilaterally [8]. It has been reported that patients with NF2 have developed schwannoma in the nasal cavity and paranasal sinuses [9]. All clinical examinations and tests of our patient were negative except the tumor located at paranasal sinus; additionally, he had neither family history nor any other signs or symptoms suggesting the suffering of NF; therefore, he was confirmed to have the relatively uncommon occurrence of sporadic form of schwannoma developing as a primary maxillary sinus lesion.

Sinonasal schwannoma, in which the nasal cavity and ethmoid sinus were more frequently involved than other paranasal sinuses [7], are commonly isolated, well-circumscribed masses, with nonspecific symptoms such as nasal obstruction, epistaxis, and anosmia, which expand along peripheral nerves. They appear to push rather than destroy the axons and degenerative changes; for instance, cystic alterations or hemorrhagic necrosis, are usually taking place. Since they have a tendency to grow slowly, the adjacent osseous structures remodeling can be secondary to benign pressure erosion.

CT imaging usually shows round expansile soft-tissue masses with the adjacent bony walls smoothly eroded and scalloped and with cystic or hemorrhagic degeneration often, especially in large tumors, without calcification generally [3]. These lumps are isoattenuating in comparison with the brain stem when undergoing unenhanced CT scan, while most of the tumors (88.9%) present a mild and patchy enhancement pattern after injecting contrast agent [10]. Imaging features are nonspecific and insufficient to allow a definitive diagnosis which could be confirmed only by pathological and immunohistochemical examination.

Postoperative histological diagnosis confirmed that the mass was a schwannoma. In the specimen two microscopic patterns, named Antoni A and Antoni B, were seen. The characteristic of Antoni A is extended spindle-shaped cells with elongated nuclei, arranged in bundles, drifts, and whorls, and Verocay bodies, while hypocellular Antoni B areas present very loose tissue composed by polymorphism of cells and abundant myxoid. In addition, scattered psammomatous calcifications were observed in specimens (Figure 3).

The immunohistochemical study showed strong and diffuse immune response for S100 protein in tumor cells and negative response for CD34 or smooth muscle actin (SMA).

Our case is distinctive because of a number of reasons. The age of our patient is unusual as most of these cases occur between the third and fifth decades of life according to reports [1113], and the youngest patient that has been well documented is just 10 years old [14]. Also this, to the best of our knowledge, is the only case reported with a wide range of calcification in the lesion showed by CT scan [3, 10, 15].

Competing Interests

The authors of this paper declared no potential competing interests with respect to the research, authorship, and publication of this article. They have no financial and personal relationships with other people or organizations that could inappropriately influence this work.


The authors thank Yan Shu (Department of Pathology) for her help in preparing the histological slides.


  1. J. N. Eble, G. Sauter, J. I. Epstein, and I. A. Sesterhenn, World Health Organization Classification of Tumours, Pathology and Genetics of Tumours of the Urinary System and Male Genital Organs, IARC Press, p. 42, 2004
  2. T. Tarik, “Schwannoma,” in Atlas of Pediatric Brain Tumors, A. M. Adesina, T. Tarik, C. E. Fuller, and T. Y. Poussaint, Eds., pp. 145–152, Springer, New York, NY, USA, 2010. View at: Google Scholar
  3. Y. Bentao, W. Zhenchang, L. Sha et al., “CT and MRI appearance of schwannoma in the sinonasal region,” Chinese Journal of Radiology, vol. 42, no. 6, pp. 618–622, 2008. View at: Google Scholar
  4. J. A. Wilson, K. McLaren, M. A. McIntyre, N. P. von Haacke, and A. G. D. Maran, “Nerve-sheath tumors of the head and neck,” Ear, Nose and Throat Journal, vol. 67, no. 2, pp. 103–110, 1988. View at: Google Scholar
  5. D. Buob, A. Wacrenier, D. Chevalier et al., “Schwannoma of the sinonasal tract: a clinicopathologic and immunohistochemical study of 5 cases,” Archives of Pathology and Laboratory Medicine, vol. 127, no. 9, pp. 1196–1199, 2003. View at: Google Scholar
  6. R. P. Hillstrom, R. J. Zarbo, and J. R. Jacobs, “Nerve sheath tumors of the paranasal sinuses: electron microscopy and histopathologic diagnosis,” Otolaryngology—Head and Neck Surgery, vol. 102, no. 3, pp. 257–263, 1990. View at: Google Scholar
  7. H. M. Hegazy, C. H. Snyderman, C.-Y. Fan, and A. B. Kassam, “Neurilemmomas of the paranasal sinuses,” American Journal of Otolaryngology—Head and Neck Medicine and Surgery, vol. 22, no. 3, pp. 215–218, 2001. View at: Publisher Site | Google Scholar
  8. G. R. Evans, S. K. W. Lloyd, and R. T. Ramsden, “Neurofibromatosis type 2,” Advances in Oto-Rhino-Laryngology, vol. 70, pp. 91–98, 2011. View at: Publisher Site | Google Scholar
  9. Y. Robitaille, T. A. Seemayer, and A. El Deiry, “Peripheral nerve tumors involving paranasal sinuses: a case report and review of the literature,” Cancer, vol. 35, no. 4, pp. 1254–1258, 1975. View at: Publisher Site | Google Scholar
  10. Y. S. Kim, H.-J. Kim, C.-H. Kim, and J. Kim, “CT and MR imaging findings of sinonasal schwannoma: a review of 12 cases,” AJNR American Journal of Neuroradiology, vol. 34, no. 3, pp. 628–633, 2013. View at: Publisher Site | Google Scholar
  11. E. Langner, A. Del Negro, H. K. Akashi, P. P. C. Araújo, A. J. Tincani, and A. S. Martins, “Schwannomas in the head and neck: retrospective analysis of 21 patients and review of the literature,” Sao Paulo Medical Journal, vol. 125, no. 4, pp. 220–222, 2007. View at: Publisher Site | Google Scholar
  12. J. Valentino, M. A. Boggess, J. L. Ellis, T. O. Hester, and R. O. Jones, “Expected neurologic outcomes for surgical treatment of cervical neurilemomas,” Laryngoscope, vol. 108, no. 7, pp. 1009–1013, 1998. View at: Publisher Site | Google Scholar
  13. S. Ganesan, R. Harar, R. Owen, R. Dawkins, and A. Prior, “Horner's syndrome: a rare presentation of cervical sympathetic chain schwannoma,” The Journal of Laryngology & Otology, vol. 111, no. 5, pp. 493–495, 1997. View at: Google Scholar
  14. T. Gökçeer, A. Yaylaci, A. C. Akkaynak, O. Peker, and O. Karaaslan, “Nasal schwannoma: a report of two cases,” Kulak Burun Bogaz Ihtisas Dergisi, vol. 13, no. 1-2, pp. 46–50, 2004. View at: Google Scholar
  15. E. Yu, D. Mikulis, and S. Nag, “CT and MR imaging findings in sinonasal schwannoma,” American Journal of Neuroradiology, vol. 27, no. 4, pp. 929–930, 2006. View at: Google Scholar

Copyright © 2016 Xiao-Hui Ma et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Related articles

No related content is available yet for this article.
 PDF Download Citation Citation
 Download other formatsMore
 Order printed copiesOrder

Related articles

No related content is available yet for this article.

Article of the Year Award: Outstanding research contributions of 2021, as selected by our Chief Editors. Read the winning articles.