Olgu Sunumu
BibTex RIS Kaynak Göster

Nadir bir senkop nedeni olarak schwannoma: Olgu sunumu

Yıl 2018, Cilt: 2 Sayı: 2, 184 - 186, 01.05.2018
https://doi.org/10.28982/josam.403858

Öz

Senkop hızlı başlangıç, kısa süre ve spontan tam iyileşme ile karakterize, geçici global serebral hipoperfüzyona bağlı bilinç kaybıdır. Senkoplu olguların dikkatli ve detaylı değerlendirilmesi gerekir. 56 yaşında erkek hastamız senkop ve kolda uyuşma şikayetleri ile başvurdu. Biz de bu vakamızda senkopun nadir bir nedeni olarak mediastinal Schwannomayı sunduk.

Kaynakça

  • 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. 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. 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. Nwazue VC, Raj SR. Confounders of vasovagal syncope: orthostatic hypotension. Cardiol Clin. 2013;31:89–100.
  • 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. 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. 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. 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.
  • 9. Macchiarini P, Ostertag H. Uncommon primary mediastinal tumours. Lancet Oncol. 2004;5:107-18.

Schwannoma as a rare cause of syncope: A case report

Yıl 2018, Cilt: 2 Sayı: 2, 184 - 186, 01.05.2018
https://doi.org/10.28982/josam.403858

Öz

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.

Kaynakça

  • 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. 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. 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. Nwazue VC, Raj SR. Confounders of vasovagal syncope: orthostatic hypotension. Cardiol Clin. 2013;31:89–100.
  • 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. 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. 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. 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.
  • 9. Macchiarini P, Ostertag H. Uncommon primary mediastinal tumours. Lancet Oncol. 2004;5:107-18.
Toplam 9 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Cerrahi, Klinik Tıp Bilimleri, İç Hastalıkları
Bölüm Olgu sunumu
Yazarlar

Serhat Sayin

Ramazan Gökdemir

Burak Bursalı

Yayımlanma Tarihi 1 Mayıs 2018
Yayımlandığı Sayı Yıl 2018 Cilt: 2 Sayı: 2

Kaynak Göster

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 Sayin S, Gökdemir R, Bursalı B. Schwannoma as a rare cause of syncope: A case report. J Surg Med. Mayıs 2018;2(2):184-186. doi:10.28982/josam.403858
Chicago Sayin, Serhat, Ramazan Gökdemir, ve Burak Bursalı. “Schwannoma As a Rare Cause of Syncope: A Case Report”. Journal of Surgery and Medicine 2, sy. 2 (Mayıs 2018): 184-86. https://doi.org/10.28982/josam.403858.
EndNote Sayin S, Gökdemir R, Bursalı B (01 Mayıs 2018) Schwannoma as a rare cause of syncope: A case report. Journal of Surgery and Medicine 2 2 184–186.
IEEE S. Sayin, R. Gökdemir, ve B. Bursalı, “Schwannoma as a rare cause of syncope: A case report”, J Surg Med, c. 2, sy. 2, ss. 184–186, 2018, doi: 10.28982/josam.403858.
ISNAD Sayin, Serhat vd. “Schwannoma As a Rare Cause of Syncope: A Case Report”. Journal of Surgery and Medicine 2/2 (Mayıs 2018), 184-186. https://doi.org/10.28982/josam.403858.
JAMA 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 vd. “Schwannoma As a Rare Cause of Syncope: A Case Report”. Journal of Surgery and Medicine, c. 2, sy. 2, 2018, ss. 184-6, doi:10.28982/josam.403858.
Vancouver Sayin S, Gökdemir R, Bursalı B. Schwannoma as a rare cause of syncope: A case report. J Surg Med. 2018;2(2):184-6.