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Schwannom; 10 yıllık tek merkez deneyimi

Year 2020, Volume: 30 Issue: 2, 92 - 97, 01.06.2020

Abstract

Amaç: Schwannomlar, Schwann hücrelerinden köken alan benign periferik sinir kılıfı tümörleridir.Sıklıkla asemptomatik, yavaş büyüyen, gerçek kapsülle çevrili, kesit yüzü pembe, beyaz-sarı renkli, genellikle küçük tümörlerdir. Bu çalışmanın amacı schwannomların görülme yaşı, cinsiyet, boyut, yerleşim yeri gibi özelliklerini ortaya koymak ve bu özellikler arasındaki ilişkiyi araştırmaktır. Gereç ve Yöntem: Konya Eğitim ve Araştırma Hastanesi Patoloji Kliniği’nde 2008-2018 yılları arasında schwannom tanısı alan hastaların verileri retrospektif olarak incelendi. Bulgular: Olguların yaş ortalaması 41.25±18.4’dür. Schwannomlar ortalama 2.96±2.1 cm çapındadır. 101 olgunun 51’i erkek, 50’si kadındır. Olguların 76’sında %75.3 tümör dermal ve subkutan, 11’inde %10.9 mediastinal, 11’inde %10.9 intraabdominal, 3’ünde %2.9 intrakranial ve spinal yerleşimlidir. Dermal ve subkutan schwannomlar DSS ’ın 39’u %51.3 ekstremite, 22’si %29 baş-boyun bölgesi, 15’i %19.7 gövde yerleşimlidir. 97 olguda tümör soliter ve sporadiktir. İntraabdominal schwannomlar İAS ’ın9’u %81.8 kadın, 2’si %18.2 erkektir. Ortalama tümör çapı DSS’da 2.32±1.58 cm, intrakraniyal ve spinal schwannomlar İKSS da 3.40±0.79 cm, mediastinal schwannomlar MS ’da 5.26±2.28 cm, İAS’da 5.00±2.62 cm’dir. MS’lu bir olguda eksizyondan bir yıl sonra tümör nüks etmiştir. Sonuç: Schwannomlar en sık 5.dekatta, genellikle 5 cm’den küçük, sıklıkla dermal ve subkutan yerleşimli olarakekstremite ve baş-boyun bölgesinde, her iki cinsiyette eşit sıklıkta, büyük çoğunluğu soliter ve sporadik olarak izlendi. İAS kadınlarda daha sıktır. DSS,MS ve İAS’lardan daha küçüktür. Nüks nadirdir.

References

  • Fletcher DM, Bridge JA, Hogendoorn PCW, Mertens F. WHO Classification of Tumours of Soft Tissue and Bo- ne.4th ed. Lyon, IARC, 2013, 169-174.
  • Srivastava A. Schwannoma. In: Mentzel T, Montgomery EA, Thway K, Lucas DR, Cassarino DS, Srivastava A. Di- agnostic Pathology Soft tissue Tumors. First ed. Altona, Amirsy, 2011; 8-12.
  • Akalın T. Schwannom. In: Dervişoğlu S, ed. Yumuşak Doku Tümörleri. İlk baskı. Ankara, Kongre Kitabevi, 2016;453- 461.
  • Nonaka D, Chiriboga L, Rubin BP. Sox10: a pan-schwannian and melanocytic marker. Am J Surg Pathol 2008;32:1291-8.
  • Gattuso P, Reddy VB, David O, Spitz DJ, Haber MH. Diffe- rential Diagnosis in Surgical Pathology. 3rd ed. Philadelp- hia, Elsevier, 2015; 288-289.
  • Kavčič J, Božič M. Schwannoma of the tongue. BMJ Case Rep 2016;2016: bcr2016215799.
  • Lee EY, Kim JJ, Seok H, Lee JY. Schwannoma of the tongue: a case report with review of literature. Maxillofac Plast Re- constr Surg 2017;39:17.
  • Hu BG, Wu FJ, Zhu J, Li XM, Li YM, Feng Y, Li HS. Gastric Schwannoma: A Tumor Must Be Included in Differential Diagnoses of Gastric Submucosal Tumors. Case Rep Gast- rointest Med 2017;2017:9615359.
  • Rodriguez E, Tellschow S, Steinberg DM, Montgomery E. Cytologic findings of gastric schwannoma: a case report. Diagnostic Cytopathology 2014;42:177-180.
  • Reid CP, Demartini W. Retroperitoneal Schwannoma: An Incidental Finding. Radiol Technol 2018;89:541-548.
  • Gueldich M, Hentati A, Chakroun A, Abid H, Kammoun S, M'saad S, Frikha I. Giant cystic schwannoma of the middle mediastinum with cervical extension. Libyan J Med 2015;10:27409.
  • Kho JPY, Prepageran N. Huge brachial plexus schwannoma, masking as a cystic neck mass. AME Case Rep 2018;2:41.
  • Cukic O, Jovanovic MB. Vagus Nerve Schwanno- ma Mimicking a Lateral Neck Cyst. J Craniofac Surg 2018;29:e827-e828.
  • Cho DH. Retroperitoneal schwannoma misdiagnosed as an ovarian malignancy. BMJ Case Rep 2018;2018: bcr-2018- 225502.

Schwannoma; 10 year single center experience

Year 2020, Volume: 30 Issue: 2, 92 - 97, 01.06.2020

Abstract

Objective: Schwannomas are benign peripheral nerve sheath tumors originating from Schwann cells. They can be seen at all ages, most common between the four and sixth decades. They are observed equally in men and women. 90% are solitary and sporadic. Schwannomas are mostly seen in the dermal and subcutaneous DS tissues, often in the extremities and head and neck region HNR . They also appear as mediastinal, retroperitoneal, spinal, intracranial and visceral tumour.Material and Methods: Patients who were diagnosed as schwannoma in the Pathology Department of Konya Training and Research Hospital between October 1 2008 and October 1 2018 were retrospectively scanned.Results: The mean age of the patients was 41.25+18.4 years. Schwannomas have a mean diameter of 2.96+2.1 cm. Of 101 cases, 51 were male and 50 were female. 76 75.3% tumors were DS, 11 10.9% were mediastinal, 11 10.9% were intraabdominal and 3 2.9% were intracranial and spinal. Of the DS schwannomas, 39 51.3% had extremity, 22 29% had HNR, 15 19.7% had trunk localisation. 11 schwannomas were cystic. In three cases, tumors were multiple. A mediastinal schwannoma recurred after one year from excision. No malignant transformation was observed in any of our cases.Conclusion: Schwannomas are mostly seen between the ages of 20-50 years in the extremities and HNR as DS tumours. In general, schwannomas are equal in both sexes. Intraabdominal schwannomas are more common in women. Schwannomas are usually smaller than 5 cm. DS schwannomas are smaller than mediastinal and intraabdominal schwannomas. Cystic schwannomas can be observed in cervical, mediastinal and retroperitoneal regions

References

  • Fletcher DM, Bridge JA, Hogendoorn PCW, Mertens F. WHO Classification of Tumours of Soft Tissue and Bo- ne.4th ed. Lyon, IARC, 2013, 169-174.
  • Srivastava A. Schwannoma. In: Mentzel T, Montgomery EA, Thway K, Lucas DR, Cassarino DS, Srivastava A. Di- agnostic Pathology Soft tissue Tumors. First ed. Altona, Amirsy, 2011; 8-12.
  • Akalın T. Schwannom. In: Dervişoğlu S, ed. Yumuşak Doku Tümörleri. İlk baskı. Ankara, Kongre Kitabevi, 2016;453- 461.
  • Nonaka D, Chiriboga L, Rubin BP. Sox10: a pan-schwannian and melanocytic marker. Am J Surg Pathol 2008;32:1291-8.
  • Gattuso P, Reddy VB, David O, Spitz DJ, Haber MH. Diffe- rential Diagnosis in Surgical Pathology. 3rd ed. Philadelp- hia, Elsevier, 2015; 288-289.
  • Kavčič J, Božič M. Schwannoma of the tongue. BMJ Case Rep 2016;2016: bcr2016215799.
  • Lee EY, Kim JJ, Seok H, Lee JY. Schwannoma of the tongue: a case report with review of literature. Maxillofac Plast Re- constr Surg 2017;39:17.
  • Hu BG, Wu FJ, Zhu J, Li XM, Li YM, Feng Y, Li HS. Gastric Schwannoma: A Tumor Must Be Included in Differential Diagnoses of Gastric Submucosal Tumors. Case Rep Gast- rointest Med 2017;2017:9615359.
  • Rodriguez E, Tellschow S, Steinberg DM, Montgomery E. Cytologic findings of gastric schwannoma: a case report. Diagnostic Cytopathology 2014;42:177-180.
  • Reid CP, Demartini W. Retroperitoneal Schwannoma: An Incidental Finding. Radiol Technol 2018;89:541-548.
  • Gueldich M, Hentati A, Chakroun A, Abid H, Kammoun S, M'saad S, Frikha I. Giant cystic schwannoma of the middle mediastinum with cervical extension. Libyan J Med 2015;10:27409.
  • Kho JPY, Prepageran N. Huge brachial plexus schwannoma, masking as a cystic neck mass. AME Case Rep 2018;2:41.
  • Cukic O, Jovanovic MB. Vagus Nerve Schwanno- ma Mimicking a Lateral Neck Cyst. J Craniofac Surg 2018;29:e827-e828.
  • Cho DH. Retroperitoneal schwannoma misdiagnosed as an ovarian malignancy. BMJ Case Rep 2018;2018: bcr-2018- 225502.
There are 14 citations in total.

Details

Primary Language Turkish
Journal Section Original Article
Authors

Meryem İlkay Eren Karanis This is me

Publication Date June 1, 2020
Published in Issue Year 2020 Volume: 30 Issue: 2

Cite

Vancouver Karanis MİE. Schwannom; 10 yıllık tek merkez deneyimi. Genel Tıp Derg. 2020;30(2):92-7.