Successful Surgical Treatment of a Giant Pulmonary Vein Ewing's Sarcoma Invading Left Atrium

2021 ◽  
Vol 57 (8) ◽  
pp. 542
Author(s):  
F. Javier González-García ◽  
José Joaquín Domínguez del Castillo ◽  
Ángel Salvatierra Velázquez
Author(s):  
F. Javier González-García ◽  
José Joaquín Domínguez del Castillo ◽  
Ángel Salvatierra Velázquez

2021 ◽  
pp. 296-302
Author(s):  
Ryosuke Hirota ◽  
Makoto Emori ◽  
Yoshinori Terashima ◽  
Kousuke Iba ◽  
Noriyuki Iesato ◽  
...  

We present the case of a 15-year-old girl. Two months after becoming aware of pain, she was diagnosed with a sacral tumor and referred to our department. She was diagnosed with a sacral Ewing’s sarcoma; after chemotherapy, it was determined that the tumor could be resected, so surgical treatment was performed. The sacrum and ilium were partially resected at the lower end of S1, and the lumbar vertebrae and pelvis were fixed with a pedicle screw and two iliac screws on each side of L3, and the sacral resection was reconstructed with a tibial strut allograft. No tumor recurrence or metastasis has been observed 1 year postoperatively. She developed bladder and rectal dysfunction, but she remained independent in activities of daily living and her daily life was not limited. The bone fusion in the reconstructed area confirmed the lack of instrumentation looseness. Surgical treatment for sacral Ewing’s sarcoma was performed to cure the patient. We believe that the tibial allograft contributed to the patient’s ability to walk on her own due to its high mechanical stability. Postoperative bone healing was observed with the same material, suggesting that the tibial allograft is useful for similar procedures.


1982 ◽  
Vol 90 (4) ◽  
pp. 491-493 ◽  
Author(s):  
Ray O. Gustafson ◽  
Nicolas E. Maragos ◽  
Herbert M. Reiman

Extraskeletal Ewing's sarcoma is a rare malignant neoplasm. Arising from a primitive mesenchymal stem cell and primarily affecting young adults, this lesion demands aggressive therapy, including surgical treatment, radiation therapy, and chemotherapy.


2009 ◽  
Vol 33 (3) ◽  
pp. 492-496 ◽  
Author(s):  
Lihui Wu ◽  
Zhifei Xu ◽  
Xuewei Zhao ◽  
Jianqiu Li ◽  
Lei Zhong ◽  
...  

2020 ◽  
Vol 19 (3) ◽  
pp. 172-179
Author(s):  
O. I. Kit ◽  
D. Yu. Yurchenko ◽  
D. V. Burtsev ◽  
S. A. Kuznetsov ◽  
O. P. Popovyan ◽  
...  

Background. Ewing’s sarcoma is one of the most common musculoskeletal cancers in children and adolescents. Extremely aggressive clinical course of Ewing’s sarcoma makes a successful treatment of this tumor difficult. Despite a comprehensive multidisciplinary approach to the treatment of this cancer, including chemotherapy, surgery and radiation therapy, rapid tumor progression, recurrence and resistance to chemotherapy are still common.Our purpose was to present the results of a personalized approach to multidisciplinary combination treatment for musculoskeletal cancer involving polychemotherapy, 3D conformal radiation therapy and modern surgical technologies.Description of the clinical case. A female patient presented to Rostov Research Institute of Oncology complaining of a tumor and moderate pain in soft tissues of the left iliac region, left lower extremity, and lameness when walking. After complete examination, the patient was diagnosed with Ewing’s sarcoma of the left ilium with lung metastases (Т3N0M1). The patient received 6 cycles of neoadjuvant chemotherapy according to EURO EWING 2008 protocol; tumor progression and lung metastasis were registered. Two cycles of second-line chemotherapy were performed; by the decision of the doctors’ council, the first stage of surgical treatment was performed: resection of the left ilium and the defect replacement with a temporary cement spacer. In the postoperative period, the patient underwent 8 cycles of adjuvant chemotherapy, external beam radiation therapy to the lungs (12 Gy total dose) and the primary tumor (46 iGy total dose), and 12 cycles of supporting therapy. A delayed second reconstructive stage of surgical treatment involved removal of a temporary cement spacer and implantation of an individual pelvic stability system. The patient was followed-up for 25 months after the combination treatment, had no complaints, and was able to ambulate without assistance; the motor function of the left hip joint was fully preserved. Conclusion. The use of non-standard high-technology approaches to surgical treatment of unfavorably localized Ewing’s Sarcoma in combination with chemo-radiation therapy allows patients with advanced tumors to achieve satisfactory results and good quality of life. 


2001 ◽  
Vol 115 (1) ◽  
pp. 74-76 ◽  
Author(s):  
Andrej Böör ◽  
Ivan Jurkovič ◽  
Imrich Friedmann ◽  
Lukás Plank ◽  
Pavol Kočan

A 20-year-old woman presented with nasal obstruction and slight epistaxis. The obstructing lesion was excised and microscopy showed a neoplasm composed of comparatively uniform undifferentiated cells forming solid nests. The cytoplasm of the cells was clear but poorly demarcated, partly vacuolated and contained much glycogen. Although widespread in the nasal mucosa, the cells did not penetrate into the underlying bone.The cells expressed the MIC2 gene (using the CD99 marker). Electron microscopy showed simple cells with a small number of mitochondria, many glycogen particles; there were no neurosecretory granules present.Early surgical treatment followed by chemo- and radiotherapy have greatly improved the prognosis of EWS: extraskeletal Ewing’s sarcoma (EWS/PNET).


2019 ◽  
Vol 27 (9) ◽  
pp. 776-778
Author(s):  
Mustafa Yılmaz ◽  
Edem Ziadinov ◽  
Hayrettin Hakan Aykan

We report the successful surgical treatment of a case of double drainage of the right upper pulmonary vein into the superior vena cava and left atrium in a 9-year-old girl.


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