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Low-grade fibromyxoid sarcoma: a rare condition with high proliferation

Yıl 2018, , 238 - 241, 04.07.2018
https://doi.org/10.18621/eurj.339764

Öz

Low-grade fibromyxoid sarcoma
(LGFMS) is a type of high metastatic potential of the fibrosarcomas. Most
of the time there is a long interval between tumor presentation and metastasis.
We present 2 cases of LGFMS. The first is a 31-year-old female with a mass in
anterior aspect of her left thigh, and the other is a 68-year-old female with
mass in posterior of her neck. Both cases underwent operation for several times
and confirmed as LGFMS histopathologically, there is no exact protocol for
postoperative follow-up to detect early metastases according to the relative variety
of LGFMS. So informing the patients about the long-standing metastatic
potential of their disease is important. 



Kaynakça

  • [1] Evans HL. Low-grade fibromyxoid sarcoma. A report of two metastasizing neoplasms having a deceptively benign appearance. Am J Clin Pathol 1987;88:615-9.
  • [2] Folpe A, van den Berg E, Molenaar WM. Low grade fibromyxoid sarcoma. In: Fletcher CDM, Unni KK, Mertens F (eds). World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. IARC Press: Lyon, 2002, pp. 104-5.
  • [3] Steiner MA, Giles HW, Daley WP. Massive low-grade fibromyxoid sarcoma presenting as acute respiratory distress in a 12-year-old girl. Pediatr Radiol 2009;39:396-9.
  • [4] Wu X, Petrovic V, Torode IP, Chow CW. Low grade fibromyxoid sarcoma: problems in the diagnosis and management of a malignant tumour with bland histological appearance. Pathology 2009;41:155-60.
  • [5] Goodlad JR, Mentzel T, Fletcher CD. Low grade fibromyxoid sarcoma: clinicopathological analysis of eleven new cases in support of a distinct entity. Histopathology 1995;26:229-37.
  • [6] Folpe AL, Lane KL, Paull G, Weiss SW. Low-grade fibromyxoid sarcoma and hyalinizing spindle cell tumor with giant rosettes: a clinicopathologic study of 73 cases supporting their identity and assessing the impact of high-grade areas. Am J Surg Pathol 2000;24:1353-60.
  • [7] Saito R, Kumabe T, Watanabe M, Jokura H, Shibuya M, Nakazato Y, et al. Low-grade fibromyxoid sarcoma of intracranial origin. J Neurosurg 2008;108:798-802.
  • [8] Kim SY, Kim M, Hwang YJ, Han YH, Seo JW, Kim YH, et al. Low grade fibromyxoid sarcoma CT, sonography, and MR findings in 3 cases. J Thorac Imaging 2005;20:294-7.
  • [9] Fujii S, Kawawa Y, Horiguchi S, Kamata N, Kinoshita T, Ogawa T. Low-grade fibromyxoid sarcoma of the small bowel mesentery: computed tomography and magnetic resonance imaging findings. Radiat Med 2008;26:244-7.
  • [10] Mohamed M, Fisher C, Thway K. Low-grade fibromyxoid sarcoma: Clinical, morphologic and genetic features. Ann Diagn Pathol 2017;28:60-7.
  • [11] Rakheja D, Seaward JR, Timmons CF. Low-grade fibromyxoid sarcoma with striking zonation. Int J Surg Pathol 2017:1066896917742724.
Yıl 2018, , 238 - 241, 04.07.2018
https://doi.org/10.18621/eurj.339764

Öz

Kaynakça

  • [1] Evans HL. Low-grade fibromyxoid sarcoma. A report of two metastasizing neoplasms having a deceptively benign appearance. Am J Clin Pathol 1987;88:615-9.
  • [2] Folpe A, van den Berg E, Molenaar WM. Low grade fibromyxoid sarcoma. In: Fletcher CDM, Unni KK, Mertens F (eds). World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone. IARC Press: Lyon, 2002, pp. 104-5.
  • [3] Steiner MA, Giles HW, Daley WP. Massive low-grade fibromyxoid sarcoma presenting as acute respiratory distress in a 12-year-old girl. Pediatr Radiol 2009;39:396-9.
  • [4] Wu X, Petrovic V, Torode IP, Chow CW. Low grade fibromyxoid sarcoma: problems in the diagnosis and management of a malignant tumour with bland histological appearance. Pathology 2009;41:155-60.
  • [5] Goodlad JR, Mentzel T, Fletcher CD. Low grade fibromyxoid sarcoma: clinicopathological analysis of eleven new cases in support of a distinct entity. Histopathology 1995;26:229-37.
  • [6] Folpe AL, Lane KL, Paull G, Weiss SW. Low-grade fibromyxoid sarcoma and hyalinizing spindle cell tumor with giant rosettes: a clinicopathologic study of 73 cases supporting their identity and assessing the impact of high-grade areas. Am J Surg Pathol 2000;24:1353-60.
  • [7] Saito R, Kumabe T, Watanabe M, Jokura H, Shibuya M, Nakazato Y, et al. Low-grade fibromyxoid sarcoma of intracranial origin. J Neurosurg 2008;108:798-802.
  • [8] Kim SY, Kim M, Hwang YJ, Han YH, Seo JW, Kim YH, et al. Low grade fibromyxoid sarcoma CT, sonography, and MR findings in 3 cases. J Thorac Imaging 2005;20:294-7.
  • [9] Fujii S, Kawawa Y, Horiguchi S, Kamata N, Kinoshita T, Ogawa T. Low-grade fibromyxoid sarcoma of the small bowel mesentery: computed tomography and magnetic resonance imaging findings. Radiat Med 2008;26:244-7.
  • [10] Mohamed M, Fisher C, Thway K. Low-grade fibromyxoid sarcoma: Clinical, morphologic and genetic features. Ann Diagn Pathol 2017;28:60-7.
  • [11] Rakheja D, Seaward JR, Timmons CF. Low-grade fibromyxoid sarcoma with striking zonation. Int J Surg Pathol 2017:1066896917742724.
Toplam 11 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Sağlık Kurumları Yönetimi
Bölüm Case Report
Yazarlar

Marzieh Karimi Khezri Bu kişi benim

M. Özgür Taşkapılıoğlu 0000-0001-5472-9065

Alper Türkkan

Ulviye Yalçınkaya

Ahmet Bekar

Yayımlanma Tarihi 4 Temmuz 2018
Gönderilme Tarihi 25 Eylül 2017
Kabul Tarihi 25 Ocak 2018
Yayımlandığı Sayı Yıl 2018

Kaynak Göster

AMA Karimi Khezri M, Taşkapılıoğlu MÖ, Türkkan A, Yalçınkaya U, Bekar A. Low-grade fibromyxoid sarcoma: a rare condition with high proliferation. Eur Res J. Temmuz 2018;4(3):238-241. doi:10.18621/eurj.339764

e-ISSN: 2149-3189 


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