Ewings sarcoma of bone in 1 case and review of literature.docVIP

 PAGE \* MERGEFORMAT 8 Ewing’s sarcoma of bone in 1 case and review of literature [Abstract] of bone Ewing’s sarcoma, treatment and prognosis features, with literature one case of pelvic bone Ewing’s sarcoma. Results, pelvic bone and soft tissue Ewing’s sarcoma is a malignant small round cell tumor, early diagnosis is difficult , rely mainly on pathological diagnosis and immunohistochemistry. The high degree of malignancy, metastasis rate and poor prognosis. comprehensive treatment can improve the 5-year survival rate. [Keywords:] bone Ewing’s sarcoma, small cell cancer, immunohistochemistry That Ewing’s tumor Ewing’s sarcoma, occurs in the lower extremity long bone .20 young century, some scholars in China for 80 years had a joint investigation, the incidence rate is about 0.6 / 10 million, accounting for 10% of malignant bone ~ 14.2% (foreign), the domestic is about 4.84% [1], while those occurring in the bone is extremely rare. in this case that occurred in the pelvic Ewing’s sarcoma of soft tissue, it is rare. now I see 1 case reported below, and review of the literature of clinical bone Ewing’s sarcoma, treatment and prognosis features. 1 Clinical data Patients, female, 15 years old. Because of the “Left pelvic mass with left lower extremity claudication pain 3 months” for treatment. Examination: the left lower abdomen, bulging, palpable quality of the hard mass, on the level of the iliac spine, medial of midline , lateral and connected to the lower pole and pelvis. pelvic B-: retroperitoneal solid mass. pelvic CT: left pelvic mass, lobulated, no bone damage. obturator see the tumor shadow, external iliac artery aneurysm was tissue surrounding the tumor shadow of L4 and the middle and lower pole of the small rotor. femoral MRI: the left side of a huge pelvic tumor size 20 cm 11 cm 10cm, enhanced scanning apparent enhancement, see no enhancement within the area, multiple nodular lesions like a combination, and the surrounding tissue ill-def