Olgu Sunumu
BibTex RIS Kaynak Göster

Multiple schwannoma unrelated with neurofibromatosis

Yıl 2020, , 53 - 57, 07.04.2020
https://doi.org/10.5505/deutfd.2020.35683

Öz

This is a report of a case of multiple schwannoma without any neurofibromatosis (NF) patterns. Patient’s history, physical examination findings, radiological and histopathological examination findings were evaluated using the records of the hospital information system and the patient’s file. The patient and his family did not have a history of NF. Excision of all symptomatic lesions was performed. Histopathological examination confirmed all lesions as schwannoma. The patient does not have a new lesion on his twenty forth postoperative month and he is satisfied with his life. The disease that is present with multiple schwannomas and that is not related with neurofibromatosis type 2 is rare. The authors recommend surgical excision for symptomatic lesions.

Kaynakça

  • Ozturk R. Bone And Soft Tissue Tumors. In: Atay T, ed. Orthopaedics And Spor Medicine, Guide For Researchers. Ankara, Derman Tıbbi Yayıncılık;2015:635–704. https://doi.org/10.4328/DERMAN.3774.
  • Daras M, Koppel BS, Heise CW, Mazzeo MJ, Poon TP, Duffy KR. Multiple spinal intradural schwannomas in the absence of Von Recklinghausens disease. Spine. 1993;18:2556–59.
  • Javalkar VK, Pigott T, Pal P, Findlay G. Multiple schwannomas: report of two cases. Eur Spine J. 2007;16(Suppl 3):287–92.
  • Ardern-Holmes S, Fisher G, North K. Neurofibromatosis Type 2. J Child Neurol. 2017; 32:9-22.
  • Haariada S, Nerlich AG, Bise K, Wiest I, Schleicher E. Comparison of various basement membrane components in benign and malignant speripheral nerve tumours. Virchows Arch A Pathol Anat Histopathol. 1992;421:331–38.
  • Woodruff JM, Godwin TA, Erlandson RA, Susin M, Martini N. Cellular schwannoma: a variety of schwannomasome times mistaken for malignant tumour. Am J Surg Pathol. 1981;5:733–44.
  • Kresak JL, Walsh M. Neurofibromatosis: A Review of NF1, NF2, and Schwannomatosis. J Pediatr Genet. 2016;5:98-104.
  • Gutman DH. The neurofibromatosis: when less is more. Hum Mol Genet. 2001;10:747–55.
  • Boyd KP, Korf BR, Theos A. Neurofibromatosis type 1. J Am Acad Dermatol. 2009;61(1):1-14.
  • Jacoby LB, Jones D, Davis K, Krann D, Short MP, Gusella J, et al. Molecular analysis of NF2 tumour suppressor gene in Schwannomatosis. Am J Hum Genet. 1997;61:1293–302.
  • Baser ME, Friedman JM, Evans DG. Increasing the specificity of diagnostic criteria for schwannomatosis. Neurology. 2006;66:730-2.
  • Öztürk R, Arıkan ŞM, Bulut EK, Kekeç AF, Çelebi F, Güngör BŞ. Distribution and evaluation of bone and soft tissue tumors operated in a tertiary care center. Acta Orthop Traumatol Turc. 2019;53:189-94.
  • Atalay İB, Şimşek MA, Irak Ö, Ekşioğlu MF, Güngör BŞ. Biological reconstruction in malignant bone tumors. Acta Oncologica Turcica. 2018;51:283-93.

NÖROFİBROMATOZİS İLİŞKİSİZ MULTIPLE SCHWANNOMA

Yıl 2020, , 53 - 57, 07.04.2020
https://doi.org/10.5505/deutfd.2020.35683

Öz

Bu yazı, nörofibromatozis (NF) özellikleri olmayan bir multiple schwannoma olgusu raporudur. Hastane bilgi sistemi kayıtları ve hasta dosyasından hastanın öyküsü, fizik muayene bulguları, radyolojik ve histopatolojik inceleme bulguları incelendi. Hastanın ve ailesinin NF öyküsü yoktu. Semptomatik lezyonların tümüne total eksizyon yapıldı. Histopatolojik inceleme, tüm lezyonları schwannom olarak doğruladı. Hastanın post-operatif on ikinci ayında yeni lezyonu yok ve yaşamından memnundur. Nörofibromatozis tip 2 ile ilişkisiz olup, multipl lezyonlar şeklinde ortaya çıkan schwannomlar nadirdir. Yazarlar semptomatik lezyonlarda cerrahi eksizyon önermektedir.

Kaynakça

  • Ozturk R. Bone And Soft Tissue Tumors. In: Atay T, ed. Orthopaedics And Spor Medicine, Guide For Researchers. Ankara, Derman Tıbbi Yayıncılık;2015:635–704. https://doi.org/10.4328/DERMAN.3774.
  • Daras M, Koppel BS, Heise CW, Mazzeo MJ, Poon TP, Duffy KR. Multiple spinal intradural schwannomas in the absence of Von Recklinghausens disease. Spine. 1993;18:2556–59.
  • Javalkar VK, Pigott T, Pal P, Findlay G. Multiple schwannomas: report of two cases. Eur Spine J. 2007;16(Suppl 3):287–92.
  • Ardern-Holmes S, Fisher G, North K. Neurofibromatosis Type 2. J Child Neurol. 2017; 32:9-22.
  • Haariada S, Nerlich AG, Bise K, Wiest I, Schleicher E. Comparison of various basement membrane components in benign and malignant speripheral nerve tumours. Virchows Arch A Pathol Anat Histopathol. 1992;421:331–38.
  • Woodruff JM, Godwin TA, Erlandson RA, Susin M, Martini N. Cellular schwannoma: a variety of schwannomasome times mistaken for malignant tumour. Am J Surg Pathol. 1981;5:733–44.
  • Kresak JL, Walsh M. Neurofibromatosis: A Review of NF1, NF2, and Schwannomatosis. J Pediatr Genet. 2016;5:98-104.
  • Gutman DH. The neurofibromatosis: when less is more. Hum Mol Genet. 2001;10:747–55.
  • Boyd KP, Korf BR, Theos A. Neurofibromatosis type 1. J Am Acad Dermatol. 2009;61(1):1-14.
  • Jacoby LB, Jones D, Davis K, Krann D, Short MP, Gusella J, et al. Molecular analysis of NF2 tumour suppressor gene in Schwannomatosis. Am J Hum Genet. 1997;61:1293–302.
  • Baser ME, Friedman JM, Evans DG. Increasing the specificity of diagnostic criteria for schwannomatosis. Neurology. 2006;66:730-2.
  • Öztürk R, Arıkan ŞM, Bulut EK, Kekeç AF, Çelebi F, Güngör BŞ. Distribution and evaluation of bone and soft tissue tumors operated in a tertiary care center. Acta Orthop Traumatol Turc. 2019;53:189-94.
  • Atalay İB, Şimşek MA, Irak Ö, Ekşioğlu MF, Güngör BŞ. Biological reconstruction in malignant bone tumors. Acta Oncologica Turcica. 2018;51:283-93.
Toplam 13 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Klinik Tıp Bilimleri
Bölüm Olgu Sunumları
Yazarlar

Recep Öztürk Bu kişi benim 0000-0002-6753-9321

Mehmet Şimşek Bu kişi benim 0000-0001-8076-8930

Ömer Ateş Bu kişi benim 0000-0002-0281-1128

Ayşe Gençoğlu Bu kişi benim 0000-0002-8843-7033

Coşkun Ulucaköy Bu kişi benim 0000-0002-6991-5511

Yayımlanma Tarihi 7 Nisan 2020
Gönderilme Tarihi 23 Ağustos 2019
Yayımlandığı Sayı Yıl 2020

Kaynak Göster

Vancouver Öztürk R, Şimşek M, Ateş Ö, Gençoğlu A, Ulucaköy C. Multiple schwannoma unrelated with neurofibromatosis. DEU Tıp Derg. 2020;34(1):53-7.