Literature DB >> 29492133

Subcutaneous Schwannoma in the Head Region.

Umit Eroglu1, Fatih Yakar1, Murat Zaimoglu1, Emre Sayaci1, Onur Ozgural1, İhsan Dogan1, Hasan Caglar Ugur1.   

Abstract

Schwannoma is a benign neural tumor derived from Schwann cells surrounding the nerves. It occurs primarily in subcutaneous tissues and muscles with a tendency for distal extremities, head, and neck area. Treatment of schwannoma is surgical excision. Lipomas are the most common soft-tissue lesions. A case is presented to increase awareness on differential diagnosis of head and neck subcutaneous masses.

Entities:  

Keywords:  Head and neck tumor; schwannoma; subcutaneous mass

Year:  2018        PMID: 29492133      PMCID: PMC5820908          DOI: 10.4103/1793-5482.185064

Source DB:  PubMed          Journal:  Asian J Neurosurg


Introduction

Schwann cell, which separates and insulates nerve cells, is a form of glial cell of the peripheral nervous system. Schwannoma is a benign, nonrecurring tumor arising from cranial nerves, bones, and gastrointestinal tract. It differentiates from Schwann cells.[1] They are also known as neurilemmoma. It occurs primarily in subcutaneous tissue and muscles with a tendency for distal extremities, head, and neck area. Treatment of schwannomas is surgical excision. Schwannomas are actually a proliferation of the nerve sheath. They are easily noticeable and hence readily separable from the tumor by careful dissection during surgical excision. True capsule is simplifying the surgical dissection. These are benign tumors and malignant transformation is very rare. The aim of our study is to present a case to increase awareness on the differential diagnosis of head and neck subcutaneous masses.

Case Report

A 23-year-old female admitted to our clinic with a painless and fast growing lesion on the scalp. She had no neurological deficits. A palpable and mobile tumor was observed on the right parietooccipital region. Computed tomography showed a lesion [Figure 1] which has a long axis of 30 mm. Radiographic imaging has provided limited information. Certain diagnosis of schwannomas is provided by histopathological study of the pathological specimen. She was operated and tumor was totally resected [Figure 2]. The streptavidin-biotin peroxidase method revealed nuclear and cytoplasmic positivity for S-100, and Ki-67 proliferation index was found to be 5%. The Antoni A and B patterns were seen. It was diagnosed as schwannoma.
Figure 1

Computed tomography scan of subcutaneous mass

Figure 2

Intraoperative view of lesion

Computed tomography scan of subcutaneous mass Intraoperative view of lesion

Discussion

Schwannoma is a neural tumor derived from Schwann cells surrounding the nerves.[1] Occurrence in the head and neck region is common.[2] Extracranial schwannomas occur in the head and neck region (25–45%).[3] They can appear at any age but are most commonly seen between the ages of 20 and 50.[4] Two-thirds of the study population were female in a study by Torossian et al. observing female predominance in extracranial cephalic schwannomas.[5] On the other hand, Leu and Chang's series shows male predominance.[6] Schwannomas often appear as painless and slow-growing tumor, without neurological symptoms initially.[7] Depending on the original nerve and localization, the mass effect can cause symptoms such as cough, dysphagia, cranial nerve paralysis, Horner syndrome, or even hearing loss.[7] The patient presented in this paper had a fast growing tumor in 3 months and had no neurological deficits. Clinically, these benign tumors are easily mistaken for other lesions such as lipoma and pleomorphic adenoma.[89] This is mainly because of their slow growth and absence of neurological symptoms. In our case, our preoperative diagnosis was lipoma. Lipomas are the most common soft-tissue tumor and contain adipose fat.[10] Hence, we did not plan a biopsy and operated with a straight incision. There was no evidence of malignancy despite the fast growing nature of lesion intraoperatively and so, we performed only lesionectomy. Metastatic or reactive lymphadenopathy, paraganglioma, angioma, carotid artery aneurysm, branchial cleft cyst, and other neurogenic tumors should be included in the differential diagnosis of schwannomas.[11]

Conclusion

An important conclusion is that the differential diagnosis of small painless nodules in the head and neck should include schwannomas.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
  11 in total

1.  Schwannoma of the tongue: report of 2 cases.

Authors:  R Pfeifle; D A Baur; A Paulino; J Helman
Journal:  J Oral Maxillofac Surg       Date:  2001-07       Impact factor: 1.895

2.  Giant ancient neurilemmoma of the cervical region: report of case.

Authors:  N Zachariades; C Skoura; G Papageorgiou; E Chrissomali
Journal:  J Oral Maxillofac Surg       Date:  2001-06       Impact factor: 1.895

3.  Schwannoma of the cervical sympathetic chain. The Virginia experience.

Authors:  R J Hood; J F Reibel; M E Jensen; P A Levine
Journal:  Ann Otol Rhinol Laryngol       Date:  2000-01       Impact factor: 1.547

4.  Head and neck schwannomas--a 10 year review.

Authors:  M P Colreavy; P D Lacy; J Hughes; D Bouchier-Hayes; P Brennan; A J O'Dwyer; M J Donnelly; R Gaffney; A Maguire; T P O'Dwyer; C V Timon; M A Walsh
Journal:  J Laryngol Otol       Date:  2000-02       Impact factor: 1.469

5.  Extracranial cephalic schwannomas: a series of 15 patients.

Authors:  J M Torossian; J L Beziat; N Abou Chebel; M Devouassoux-Shisheboran; G Fischer
Journal:  J Craniofac Surg       Date:  1999-09       Impact factor: 1.046

6.  Clinical characteristics and treatment outcome for nonvestibular schwannomas of the head and neck.

Authors:  James P Malone; Wha-Joon Lee; Roger J Levin
Journal:  Am J Otolaryngol       Date:  2005 Mar-Apr       Impact factor: 1.808

7.  Extracranial head and neck schwannomas: a review of 8 years experience.

Authors:  Y S Leu; K C Chang
Journal:  Acta Otolaryngol       Date:  2002-06       Impact factor: 1.494

Review 8.  From the archives of the AFIP: benign musculoskeletal lipomatous lesions.

Authors:  Mark D Murphey; John F Carroll; Donald J Flemming; Thomas L Pope; Francis H Gannon; Mark J Kransdorf
Journal:  Radiographics       Date:  2004 Sep-Oct       Impact factor: 5.333

9.  Sciatic nerve schwannoma: case report.

Authors:  Umit Eroglu; Melih Bozkurt; Ozgur Ozates; Seda Akturk; Hakan Tuna
Journal:  Turk Neurosurg       Date:  2014       Impact factor: 1.003

10.  Diagnosis and management of extracranial head and neck schwannomas: a review of 27 cases.

Authors:  Ryuji Yasumatsu; Torahiko Nakashima; Rina Miyazaki; Yuichi Segawa; Shizuo Komune
Journal:  Int J Otolaryngol       Date:  2013-05-08
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