Case Report

Schwannoma as a rare cause of syncope: A case report

Volume: 2 Number: 2 May 1, 2018
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Schwannoma as a rare cause of syncope: A case report

Abstract

Syncope is a loss of consciousness due to transient global cerebral hypoperfusion and characterized by rapid onset, short term and spontaneous complete recovery. The cases with syncope need to be carefully and thoroughly evaluated. Our patient who is 56 year old male was admitted with complaints of syncope and hand numbness. We presented mediastinal schwannoma as a rare cause of syncope in our case.

Keywords

References

  1. 1. Brignole M, Alboni P, Benditt D, Bergfeldt L, Blanc JJ, Bloch Thomsen PE, et al. Guidelines on management (diagnosis and treatment) of syncope. Eur Heart J 2001;22:1256-306.
  2. 2. Calkins H, Shyr Y, Frumin H, Schork A, Morady F. The value of the clinical history in the differentiation of syncope due to ventricular tachycardia, atrioventricular block, and neurocardiogenic syncope. Am J Med. 1995;98:365–73.
  3. 3. Soteriades ES, Evans JC, Larson MG, Chen MH, Chen L, Benjamin EJ, et al. Incidence and prognosis of syncope. N Engl J Med. 2002;347 (12):878–85.
  4. 4. Nwazue VC, Raj SR. Confounders of vasovagal syncope: orthostatic hypotension. Cardiol Clin. 2013;31:89–100.
  5. 5. Strollo DC, Rosado-de-Christenson ML, Jett JR. Primary mediastinal tumors. Part II. Tumors of the middle and posterior mediastinum. Chest. 1997;112:1344–57.
  6. 6. Martin-Ucar AE, Rengarajan A, Waller DA. Giant intercostal nerve Schwannoma presenting as Horner’s syndrome. Recovery after surgical resection. Eur J Cardiothorac Surg. 2002;22:310.
  7. 7. Reynolds M, Shields TW. Benign and malignant neurogenic tumors of the mediastinum in children and in adults. In: Shields TW, editor. General thoracic surgery. 6th ed. Philadelphia; William & Wilkins; 2004. p. 2729-56.
  8. 8. Molenaar WM, Ladde BE, Schraffordt Koops H, DamMeiring A. Two epithelioid malignant schwannomas in a patient with neurofibromatosis. Cytology, histology and DNA-flow-cytometry. Pathol Res Pract. 1989;184:529-34.

Details

Primary Language

English

Subjects

Surgery , Clinical Sciences , ​Internal Diseases

Journal Section

Case Report

Publication Date

May 1, 2018

Submission Date

March 9, 2018

Acceptance Date

April 8, 2018

Published in Issue

Year 2018 Volume: 2 Number: 2

APA
Sayin, S., Gökdemir, R., & Bursalı, B. (2018). Schwannoma as a rare cause of syncope: A case report. Journal of Surgery and Medicine, 2(2), 184-186. https://doi.org/10.28982/josam.403858
AMA
1.Sayin S, Gökdemir R, Bursalı B. Schwannoma as a rare cause of syncope: A case report. J Surg Med. 2018;2(2):184-186. doi:10.28982/josam.403858
Chicago
Sayin, Serhat, Ramazan Gökdemir, and Burak Bursalı. 2018. “Schwannoma As a Rare Cause of Syncope: A Case Report”. Journal of Surgery and Medicine 2 (2): 184-86. https://doi.org/10.28982/josam.403858.
EndNote
Sayin S, Gökdemir R, Bursalı B (May 1, 2018) Schwannoma as a rare cause of syncope: A case report. Journal of Surgery and Medicine 2 2 184–186.
IEEE
[1]S. Sayin, R. Gökdemir, and B. Bursalı, “Schwannoma as a rare cause of syncope: A case report”, J Surg Med, vol. 2, no. 2, pp. 184–186, May 2018, doi: 10.28982/josam.403858.
ISNAD
Sayin, Serhat - Gökdemir, Ramazan - Bursalı, Burak. “Schwannoma As a Rare Cause of Syncope: A Case Report”. Journal of Surgery and Medicine 2/2 (May 1, 2018): 184-186. https://doi.org/10.28982/josam.403858.
JAMA
1.Sayin S, Gökdemir R, Bursalı B. Schwannoma as a rare cause of syncope: A case report. J Surg Med. 2018;2:184–186.
MLA
Sayin, Serhat, et al. “Schwannoma As a Rare Cause of Syncope: A Case Report”. Journal of Surgery and Medicine, vol. 2, no. 2, May 2018, pp. 184-6, doi:10.28982/josam.403858.
Vancouver
1.Serhat Sayin, Ramazan Gökdemir, Burak Bursalı. Schwannoma as a rare cause of syncope: A case report. J Surg Med. 2018 May 1;2(2):184-6. doi:10.28982/josam.403858

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