肉瘤

Most of them are low grade or well differentiated liposarcoma (rather than the myxoid or pleomorphic variants of liposarcomas).

大部分都属于低级别或分化良好型脂肪肉瘤（而非粘液型或多形性脂肪肉瘤）。

Results:The tumor was divided into two histologic subtypes:biphasic type(4 cases) and monophasic type(1 case).

结果 ：组织学检查分为双相性SRCC 4例，由癌和肉瘤样成分组成；单相性 1例，由差分化的肉瘤样梭形细胞、单核细胞与破骨细胞样多核巨细胞组成。

Results: Most synovial sarcomas located in the extremities close to joints. Synovial sarcomas detected by radiography typically appeared as round, oval or multilobulated juxtaarticular soft-tissue masses with calcification in some cases. The most common CT appearance of synovial sarcoma was heterogeneous deep -seated soft-tissue mass with attenuation similar to or slightly lower than that of muscle. On T1WI, synovial sarcomas typically appeared as prominently heterogeneous multilobulated soft tissue masses with signal intensity similar to or slightly higher than that of muscle. On T2WI, synovial sarcomas appeared as prominent heterogeneity with predominantly high signal intensity.

结果：大部分滑膜肉瘤位于关节旁；X线表现为圆形、椭圆形或分叶状软组织肿块，部分可见肿块内钙化；典型的CT表现为较深在的、等或稍低密度不均匀的软组织肿块；磁共振T1WI与肌肉信号相比，滑膜肉瘤表现为分叶状、不均匀、等或稍高信号，T2WI则表现为高信号为主的不均匀信号；DSA呈显著的肿瘤实体染色及新生血管。

Altogether, approximately 50 bona fide liposarcomas have been reported in children and adolescents, most of which have represented myxoid liposarcomas, with a good prognosis.

文献中大约总共报道了50例发生于儿童和青少年的真性脂肪肉瘤，其中大部分是黏液样脂肪肉瘤，且预后良好。

The postoperative pathology confirmed that cortical carcinoma was found in 5 cases and pheochromocytoma in 20 cases, malignant pheochromocytoma in 4 cases, malignant fibrous histiocytoma in 1 case, neurocytoma in 1 case, myelolipoma in 1 case, dysembryoma in 1 case, dysembryo-sarcoma in 1 case, well-differentiated liposarcoma in 1 case respectively.

术后病理提示皮质癌5例；嗜铬细胞瘤20例；恶性pheo 4例；恶性纤维组织细胞瘤1例；节神经细胞瘤1例；髓样脂肪瘤1例；畸胎瘤1例；畸胎肉瘤1例；高分化脂肪肉瘤1例。

The appearances of nonvascular lesions were as the following : solitary, huge cystic lesions with wall and septa obvious enhancement were found in malignant enbryonal sarcoma; mixed density mass with necrotic cystic change and solid portion enhanced obviously in carcinosarcoma; intrahepatic huge low density, cystic changes, calcification and margin enhancement were found in leiomyosarcoma.

血管源性表现为肝内多发低密度灶，强化明显，非血管源性表现为肝内巨大单发囊性病灶，增强囊壁和分隔明显强化；癌肉瘤表现为混杂密度肿块伴有坏死囊变，增强实质部分强化；平滑肌肉瘤表现为肝内巨大低密度病灶，可伴有囊变及钙化，增强见边缘强化。

Results: The expressing rate of OPG was significant different between osteosarcoma and osteochondroma.

结果： 骨肉瘤与骨软骨瘤OPG的表达有显著性差异，骨肉瘤与骨软骨瘤OPGL的表达无显著性差异。

Methods: The immunohistochemistry was used to investigate the protein expression of p27 in 46 cases of osteosarcoma and 16 cases of osteochondroma. The expression of p27 and histological category and differentiation levels of osteosarcoma were observed.

应用S-P免疫组织化学方法检测46例骨肉瘤和16例骨软骨瘤组织中p27的表达，并观察p27表达在骨肉瘤组织学分型、分化程度等临床指标之间的差异。

Both cyclin D1 and cdk4 were present in 1/ 8 (12.5%) osteochondroma of the jaws.

结果 软骨肉瘤cyclin D1和cdk4阳性表达率分别为70%（14/ 20）和65%（13/20），二者的阳性表达存在正相关（rs= 0.526， P 0.05）；而它们在骨软骨瘤的阳性表达率均为12.5%（1/ 8），在软骨瘤无表达，与软骨肉瘤相比有显著性差异（P 0.05）。

The expressing rate of OPG was not significant different between osteosarcoma and osteochondroma.

骨肉瘤中存在OPG高表达，可能与骨肉瘤的成骨性有关。

They weren't aggressive, but I yelled and threw a rock in their direction to get them off the trail and away from me, just in case.

他们没有侵略性，但我大喊，并在他们的方向扔石头让他们过的线索，远离我，以防万一。

In slot 2 in your bag put wrapping paper, quantity does not matter in this case.

在你的书包里槽2把包装纸、数量无关紧要。