BibTex RIS Cite

Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası

Year 2019, Volume: 19 Issue: 1, 48 - 50, 01.04.2019
https://doi.org/10.5222/j.child.2019.93275

Abstract

On yedi yaşında kız hasta, karaciğerde dört farklı segmentte insidental olarak saptanmış epiteloid hemanjioendotelyoma tanısıyla tarafımıza yönlendirildi. Karaciğer tru-cut biyopsi materyalinin yeniden incelenmesi sonucunda epiteloid hemanjioendotelyoma ile uyumlu olduğu görüldü. Yapılan tetkiklerinde akciğer ve beyinde multipl metastatik odaklar saptanan hasta asemptomatik olduğundan tedavisiz izlemine karar verildi. Bir yıllık izlem süresi boyunca herhangi bir semptomu olmayan hastamızın bir yıl sonundaki kontrol görüntülemelerinde kitlelerin boyutlarının artmadığı ve yeni bir metastaz olmadığı görüldü. Multipl metastazı olan epiteloid hemanjioendotelyoma vakaları için bevacizumab terapisi veya cerrahi tedavi yöntemleri uygulanabilmektedir. Hastamızın seyri, kitle boyutlarına ve metastaz yaygınlığına bakılmaksızın, asemptomatik epiteloid hemanjioendotelyoma hastalarının tedavisiz izlemi için cesaret verici olmuştur.

References

  • 1. Celikel C, Yumuk PF, Basaran G, Yildizeli B, Kodalli N, Ahiskali R. Epithelioid hemangioendothelioma with multiple organ involvement. Apmis. 2007;115:881-8.
  • 2. Sardaro A, Bardoscia L, Petruzzelli MF, Portaluri M. Epithelioid hemangioendothelioma: an overview and update on a rare vascular tumor. Oncology reviews, 2014;8:2.
  • 3. Abdalla A, Seedahmed E, Bachuwa G, Congdon D. Lung lobar collapse as the first manifestation of pulmonary epithelioid haemangioendothelioma diagnosed with fibreoptic bronchoscopy. BMJ Case Rep. 2016;4:11.
  • 4. Yang J W, Li Y, Xie K, Dong W, Cao X T, Xiao W D. Spontaneous rupture of hepatic epithelioid hemangioendothelioma: A case report. World J Gastroenterol. 2017;23:185.
  • 5. Mehrabi A, Kashfi A, Fonouni H, et al. Primary malignant hepatic malignant hepatic epithelioid hemangioendothelioma a comprehensive review of the literatüre with emphasis on the surgical therapy, Cancer 2007;107:2108-21.
  • 6. Agulnik M, Yarber JL, Okuno SH, et al. An open-label, multicenter, phase II study of bevacizumab for the treatment of angiosarcoma and epithelioid hemangioendotheliomas. Ann Oncol. 2013;24:257-63.
  • 7. Ishak KG, Sesterhenn IA, Goodman MZD, Rabin L, Stromeyer FW. Epithelioid hemangioendothelioma of the liver: a clinicopathologic and follow-up study of 32 cases. Hum Pathol. 1984;15:839-52.

A Rare Neoplastic Disease of Childhood: Multifocal Epithelioid Hemangioendothelioma

Year 2019, Volume: 19 Issue: 1, 48 - 50, 01.04.2019
https://doi.org/10.5222/j.child.2019.93275

Abstract

A 17-year-old girl in whom the diagnosis of epithelioid hemangioendothelioma was established in four different segments of the liver incidentally was referred to us. Further examination of tru-cut biopsy material showed multiple metastatic lesions in the brain and both lungs. Since the patient was asymptomatic, she was followed up without treatment for a year. At the first-year control visit, the radiologic examination indicated a stable epithelioid hemangioendothelioma without any new metastatic lesion, and increase in the dimensions of the mass lesion. The management of epithelioid hemangioendothelioma consists of surgical treatment, drug administration such as bevacizumab or follow-up without treatment. The course of the disease in our patient encouraged follow-up of asymptomatic patients with epithelioid hemangioendothelioma without treatment, regardless of the extent of metastatic lesions,and dimensions of the mass lesion

References

  • 1. Celikel C, Yumuk PF, Basaran G, Yildizeli B, Kodalli N, Ahiskali R. Epithelioid hemangioendothelioma with multiple organ involvement. Apmis. 2007;115:881-8.
  • 2. Sardaro A, Bardoscia L, Petruzzelli MF, Portaluri M. Epithelioid hemangioendothelioma: an overview and update on a rare vascular tumor. Oncology reviews, 2014;8:2.
  • 3. Abdalla A, Seedahmed E, Bachuwa G, Congdon D. Lung lobar collapse as the first manifestation of pulmonary epithelioid haemangioendothelioma diagnosed with fibreoptic bronchoscopy. BMJ Case Rep. 2016;4:11.
  • 4. Yang J W, Li Y, Xie K, Dong W, Cao X T, Xiao W D. Spontaneous rupture of hepatic epithelioid hemangioendothelioma: A case report. World J Gastroenterol. 2017;23:185.
  • 5. Mehrabi A, Kashfi A, Fonouni H, et al. Primary malignant hepatic malignant hepatic epithelioid hemangioendothelioma a comprehensive review of the literatüre with emphasis on the surgical therapy, Cancer 2007;107:2108-21.
  • 6. Agulnik M, Yarber JL, Okuno SH, et al. An open-label, multicenter, phase II study of bevacizumab for the treatment of angiosarcoma and epithelioid hemangioendotheliomas. Ann Oncol. 2013;24:257-63.
  • 7. Ishak KG, Sesterhenn IA, Goodman MZD, Rabin L, Stromeyer FW. Epithelioid hemangioendothelioma of the liver: a clinicopathologic and follow-up study of 32 cases. Hum Pathol. 1984;15:839-52.
There are 7 citations in total.

Details

Primary Language Turkish
Journal Section Case Report
Authors

Özge Bayrak Demirel This is me

Serap Karaman This is me

Ayşe Özkan Karagenç This is me

Deniz Tuğcu This is me

İbrahim Adaletli This is me

Rejin Kebudi This is me

Ayşegül Ünüvar This is me

Zeynep Karakaş This is me

Publication Date April 1, 2019
Published in Issue Year 2019 Volume: 19 Issue: 1

Cite

APA Bayrak Demirel, Ö., Karaman, S., Özkan Karagenç, A., Tuğcu, D., et al. (2019). Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası. Journal of Child, 19(1), 48-50. https://doi.org/10.5222/j.child.2019.93275
AMA Bayrak Demirel Ö, Karaman S, Özkan Karagenç A, Tuğcu D, Adaletli İ, Kebudi R, Ünüvar A, Karakaş Z. Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası. Journal of Child. April 2019;19(1):48-50. doi:10.5222/j.child.2019.93275
Chicago Bayrak Demirel, Özge, Serap Karaman, Ayşe Özkan Karagenç, Deniz Tuğcu, İbrahim Adaletli, Rejin Kebudi, Ayşegül Ünüvar, and Zeynep Karakaş. “Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası”. Journal of Child 19, no. 1 (April 2019): 48-50. https://doi.org/10.5222/j.child.2019.93275.
EndNote Bayrak Demirel Ö, Karaman S, Özkan Karagenç A, Tuğcu D, Adaletli İ, Kebudi R, Ünüvar A, Karakaş Z (April 1, 2019) Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası. Journal of Child 19 1 48–50.
IEEE Ö. Bayrak Demirel, “Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası”, Journal of Child, vol. 19, no. 1, pp. 48–50, 2019, doi: 10.5222/j.child.2019.93275.
ISNAD Bayrak Demirel, Özge et al. “Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası”. Journal of Child 19/1 (April 2019), 48-50. https://doi.org/10.5222/j.child.2019.93275.
JAMA Bayrak Demirel Ö, Karaman S, Özkan Karagenç A, Tuğcu D, Adaletli İ, Kebudi R, Ünüvar A, Karakaş Z. Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası. Journal of Child. 2019;19:48–50.
MLA Bayrak Demirel, Özge et al. “Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası”. Journal of Child, vol. 19, no. 1, 2019, pp. 48-50, doi:10.5222/j.child.2019.93275.
Vancouver Bayrak Demirel Ö, Karaman S, Özkan Karagenç A, Tuğcu D, Adaletli İ, Kebudi R, Ünüvar A, Karakaş Z. Çocukluk Çağının Ender Bir Neoplastik Hastalığı: Multifokal Epiteloid Hemanjioendotelyoma Vakası. Journal of Child. 2019;19(1):48-50.