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A middle mediastinal schwannoma: A rare case report

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Turkish Journal of Thoracic and Cardiovascular Surgery 2021;29(2):283-284 http://dx.doi.org/doi: 10.5606/tgkdc.dergisi.2021.20195

A middle mediastinal schwannoma: A rare case report

Orta mediasten yerleşimli schwannoma: Nadir bir olgu sunumu Buse Mine Konuk1, Süleyman Gökalp Güneş1, Yusuf Kahya1, Koray Ceyhan2, Serkan Enon1

1Department of Thoracic Surgery, Ankara University School of Medicine, Ankara, Turkey

2Department of Pathology, Division of Cytopathology, Ankara University, School of Medicine, Ankara, Turkey

Received: May 28, 2020 Accepted: September 01, 2020 Published online: April 26, 2021

Correspondence: Süleyman Gökalp Güneş, MD. Ankara Üniversitesi Tıp Fakültesi Göğüs Cerrahisi Anabilim Dalı, 06590 Çankaya, Ankara, Türkiye.

Tel: +90 312 - 508 31 65 e-mail: [email protected]

©2021 All right reserved by the Turkish Society of Cardiovascular Surgery.

This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes (http://creativecommons.org/licenses/by-nc/4.0/).

Konuk BM, Güneş SG, Kahya Y, Ceyhan K, Enon S. A middle mediastinal schwannoma: A rare case report. Turk Gogus Kalp Dama 2021;29(2):283-284

Cite this article as:

A 55-year-old female patient presented with chest pain for two months. Her medical history revealed previous breast cancer and thyroid cancer. Physical examination and laboratory test results showed no significant abnormalities. Thoracic posteroanterior X-ray and computed tomography (CT) showed a mass of 43¥33 mm in size with regular contours located in the middle mediastinum. Positron emission tomography (PET) showed 18F-fluorodeoxyglucose (FDG) uptake with a maximum standardized uptake

value (SUVmax) of 9.1 (Figure 1a-c). A written

informed consent was obtained from the patient and she underwent endobronchial ultrasound (EBUS) transbronchial needle aspiration (TBNA) for the diagnosis of the mass. Cytopathological examination was reported as a benign nerve sheath tumor (schwannoma) (Figure 2a-c). The patient was offered the surgical excision; however, she refused any surgical intervention. Subsequent follow-ups with

thoracic CT did not show any progression of the mass. However, there was an increase in the SUVmax after 36 months. The patient is still under follow-up in the medical oncology clinic.

Mediastinal nerve sheath tumors commonly originate from intercostal nerves and sympathetic chain located at the posterior mediastinum.[1] Recent

studies have documented nerve sheath tumors to arise, although less frequently, from the vagus nerve, phrenic nerve, and recurrent nerve areas outside of the posterior mediastinum.[2-4] Schwannomas are benign

nerve sheath tumors of Schwann cell origin and are the most common of the neurogenic mediastinal tumors. Although they primarily arise from posterior mediastinum, they should be considered in the differential diagnosis of middle mediastinal masses. The definitive treatment for schwannomas is surgical resection with a low recurrence rate.

Figure 1. (a) Preoperative PA lung X-ray. (b) Preoperative axial thorax CT image. (c) Preoperative coronal thorax CT image. (d) Preoperative axial PET-CT image. (e) Preoperative coronal PET-CT image.

PA: Posteroanterior; CT: Computed tomography; PET: Positron emission tomography.

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Turk Gogus Kalp Dama 2021;29(2):283-284

Declaration of conflicting interests

The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

Funding

The authors received no financial support for the research and/or authorship of this article.

REFERENCES

1. Wang W, Cui M, Ma HX, Zhang H, Zhang ZH, Cui YB. A large schwannoma of the middle mediastinum: A case report

and review of the literature. Oncol Lett 2016;11:1719-21. 2. Rammos KS, Rammos SK, Foroulis CN, Zaramboukas TK.

Schwannoma of the vagus nerve, a rare middle mediastinal neurogenic tumor: Case report. J Cardiothorac Surg 2009;4:68.

3. D'Souza B, Lowe A, Stewart B, Roberts T. A rare case of Schwannoma of the intrathoracic phrenic nerve. ANZ J Surg 2010;80:841-2.

4. Sasaki K, Kohno T, Mun M, Yoshiya T. Thoracoscopic removal of middle mediastinal schwannoma originating from recurrent nerve. Thorac Cardiovasc Surg 2008;56:375-7.

Figure 2. (a) EBUS/TBNA smear showing collapsed spindle mesenchymal cells in the collagen matrix, MGG, ¥11.6

(May-Grünwald-Giemsa stain ¥ objective magnification H-E, ¥11.6. (b) Spindle cell mesenchymal tumor in the cell block obtained from cytological material, H-E, ¥11.6. (c) Widespread S-100 positivity in tumor cells in cell block immunocytochemistry.

EBUS: Endobronchial ultrasound; FNAB: Fine needle aspiration biops; TBNA: Transbronchial needle aspiration; H-E: Hematoxylin and eosin.

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