Skip to main content
Clinical Case Reports logoLink to Clinical Case Reports
. 2019 Oct 31;7(12):2585–2587. doi: 10.1002/ccr3.2274

Benign posterior mediastinal schwannoma—Multiple diagnostic imaging modalities

Yeo‐Jeong Song 1, Sang‐Hoon Seol 1,, Seunghwan Kim 1, Dong‐Kie Kim 1, Ki‐Hun Kim 1, Doo‐Il Kim 1, Do‐Kyun Kang 2, Ji Yeon Kim 3
PMCID: PMC6935620  PMID: 31893108

Abstract

Schwannoma is usually benign, encapsulated spindle cell tumor which arises from schwann cells of nerve sheath, and is the most common of the neurogenic mediastinal tumors. Various imaging modalities can be applied to assess posterior mediastinal mass which is often found incidentally without symptom and frequently misdiagnosed for other benign conditions both clinically and radiologically in which clinicians should be aware of.

Keywords: diagnostic modalities, mediastinal schwannoma


Schwannoma is usually benign, encapsulated spindle cell tumor which arises from schwann cells of nerve sheath, and is the most common of the neurogenic mediastinal tumors. Various imaging modalities can be applied to assess posterior mediastinal mass which is often found incidentally without symptom and frequently misdiagnosed for other benign conditions both clinically and radiologically in which clinicians should be aware of.

graphic file with name CCR3-7-2585-g005.jpg

1. INTRODUCTION

Neural originate tumors are the most common primary mediastinal neoplasms. A large proportion of them are benign. Schwannomas are the most common type of neurogenic tumor observed in thorax which originated from the peripheral nerve sheath of Schwann cells and often located in the posterior mediastinum.1 It is frequently found incidentally as an asymptomatic mass by various imaging modalities.2 We report a case of incidental schwannoma in middle‐aged woman who was treated successfully by complete surgical resection of the mass.

2. CASE HISTORY

A 60‐year‐old woman with cough was referred to our hospital for general check‐up. The patient had no pathologic symptom and underlying disease. Chest X‐ray showed an incidental mediastinal mass in posterior cardia area (Figure 1A). Transthoracic echocardiography showed well‐defined heterogeneous oval mass compressing left atrium (Figure 2). Gastroendoscopy revealed a huge bulging subepithelial mass at the distal esophagus, which was extended to mid esophagus (Figure 3). Chest computed tomography (CT) demonstrated a hypodense oval mass of 7.4 × 4.5 cm size in the posterior mediastinum. The mass compressed the left atrium, esophagus without definite invasion to lung (Figure 1B). After verifying the mass localization, the patient underwent surgical excision. The gross finding of the tumor showed well localized white and yellowish soft mass with extensive myxoid degeneration and multiple focal hemorrhages (Figure 4A). Immunohistochemical staining demonstrated the groups of spindle cells (S100, ×200) with waxy nuclei which strongly suggested a histopathologic finding of the benign schwannoma (Figure 4B). No marginal invasion was observed. The patient was eventually discharged from the hospital without any complication.

Figure 1.

Figure 1

Chest X‐ray showed mediastinal mass in posterior cardia area (A). The chest computed tomography showed an oval shaped mass of 7.4 × 4.5 cm size in the posterior mediastinum. The mass compressed the left atrium, esophagus, and no definite invasion to lung (B)

Figure 2.

Figure 2

Transthoracic echocardiography revealed well‐defined heterogeneous oval mass compressing left atrium in the parasternal long (A) and short axis view (B). LA, left atrium

Figure 3.

Figure 3

Gastrofibroscopy demonstrated a huge bulging mass at the distal esophagus

Figure 4.

Figure 4

The pathology demonstrated that microscopic finding revealed white/yellow, soft mass with extensive myxoid degeneration and focal hemorrhage (A). Immunohistochemical staining showed that tumor cells were strongly positive staining for spindle cells (S100, ×200) (B)

3. DISCUSSION

Schwannoma is the most common benign neurogenic tumor that originated from the peripheral nerve sheath of Schwann cells. Intrathoracic schwannoma is most frequently located in the posterior mediastinum.1 It is usually slow growing mass with low potency of malignancy. In terms of rare cases of malignant deformation, broad fusiform typed pleomorphic spindle cells may exist with necrotic and hemorrhagic changes.3 Alike above case, it is incidentally found as an asymptomatic mass on the imaging studies such as echocardiography, gastroendoscopy, and chest CT.2 Clinical symptoms may not appear until surrounding organs have been invaded or compressed by the tumor. CT may be helpful in confirming the extension and respectability of the tumor.4 Complete surgical excision is the treatment of choice for mediastinal schwannoma because of virtual pulmonary complications intruding intercartilaginous membrane of trachea causing hemoptysis, dyspnea, or chest pain.2 The other complication may involve gastrointestinal bleeding, cardiac tamponade, and dysphonia in severe cases. Approximately 10% of the cases may invade intervertebral foramen which results in the compression of vertebral canal.5 Fortunately, the successful complete surgical resection was done in above patient without any need of adjuvant chemotherapy. Various imaging modalities can be applied to assess posterior mediastinal mass which is often found incidentally without symptom and frequently misdiagnosed for other benign conditions in which clinicians should take heed of.

CONFLICT OF INTEREST

None declared.

AUTHOR CONTRIBUTIONS

YJS: involved in literature search and the writing of the manuscript. SHS: investigated and supervised the overall work. SK, DKK, KHK, and DIK: discussed the results and advised about the case. Do‐Kyun K: performed the operation and provided surgical information. JYK: provided pathological information and images.

Song Y‐J, Seol S‐H, Kim S, et al. Benign posterior mediastinal schwannoma—Multiple diagnostic imaging modalities. Clin Case Rep. 2019;7:2585–2587. 10.1002/ccr3.2274

REFERENCES

  • 1. Heras F, Ramos G, Castanedo M, Cortejoso A, Duque JL, Yuste MG. Schwannoma of the intrathoracic vagus nerve. Arch Bronconeumol. 1997;33:360‐362. [DOI] [PubMed] [Google Scholar]
  • 2. Kato M, Shiota S, Shiga K, et al. Benign giant mediastinal schwannoma presenting as cardiac tamponade in a woman: a case report. J Med Case Rep. 2011;5:61. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Andreas K, Rainer R, Anika P, Detlef B. Giant intrathoracic left‐sided vagal schwannoma. Thorac Cardiovasc Surg Rep. 2013;2:19‐22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4. Razafimanjato N, Ravoatrarilandy M, Hunald FA, Rajaonera TA, Rakotovao H. An unusual presentation of massive intrathoracic schwannoma with concomittant pleural tuberculosis: about a case and review of the literature. Austin J Pulm Respir Med. 2018;5:1058. [Google Scholar]
  • 5. Georghiou GP, Vidne BA, Boikov O, Milton S. Giant schwannoma of the posterior mediastinum. Eur J Cardiothorac Surg. 2003;24:1030. [DOI] [PubMed] [Google Scholar]

Articles from Clinical Case Reports are provided here courtesy of Wiley

RESOURCES