查询词典 liposarcoma

Resulte: In 12 infective lesions, including purulent infection (4 cases) and tuberculosis (8 cases), the correct dignosis was made in 4cases by CR and in 11 cases by CT. In 16 soft tissue tumors, including lipoma (7 cases), fibrosarcoma (4 cases), hemangioma (1 case), neurofibroma (1 case), malignant fibrous histocytoma (1case), aggressive fibromatosis (1 case) and liposarcoma (1 case), the correct diagnosis was made in 3cases by CR and in 14 cases by CT. In 11 bone lesions, including fibrous dysplasia (7 cases), chondroma (2 cases), myeloma and cosinophilic granuloma (1 case), the correct diagnosis was made in 8cases by CR and in 10 cases by CT.

结果：感染组12例中(包括化脓性感染4例，胸壁结核8例)，CR准确诊断4例，CT诊断11例；软组织肿瘤组16例中(包括脂肪瘤7例，纤维肉瘤4例，血管瘤、神经纤维瘤、恶性纤维组织细胞瘤、侵袭性纤维瘤病和脂肪肉瘤各l例)，CR准确诊断3例，CT诊断14例；骨肿瘤和肿瘤样病变组11例中(包括骨纤维异常增殖症7例，软骨瘤2例，多发性骨髓瘤和骨嗜酸性肉芽肿各1例)，CR准确诊断8例，CT诊断10例。

The corelation of CT signs of different histological liposarcoma with pathology was studied.

分析不同组织类型脂肪肉瘤的CT表现与病理的相关性。

Their feature on histology not is apparently, well differentiated liposarcoma with well fattiness tumor as well as dedifferentiated liposarcoma with malignant shuttle shape / much shape do not break up tumor distinguish is still a baffling problem.

它们在组织学士特征不是很明显，高分化与良性脂肪性肿瘤以及去分化与恶性梭形／多形未分化肿瘤的鉴别仍是一个难题。

Methods The clinical data of 58 patients with SS(including liomysarcoma 44 cases,malignant lymphosarcoma 11 cases,neurofibrosarcoma 2 cases,liposarcoma 1 case) were analysed.

回顾性分析58例胃肉瘤(其中平滑肌肉瘤44例，恶性淋巴瘤11例，神经纤维瘤2例，脂肪肉瘤1例)患者的临床资料。

Some of the laryngeal MFH were difficult to be differentiated from carcinosarcoma, pleomorphic rhabdomyosarcoma , myxoid liposarcoma ,malignant neurilemmoma and myxoma without immunohistochemical aids .

喉恶性纤维组织细胞瘤常规组织学与癌肉瘤、多形性横纹肌肉瘤、粘液型脂肪肉瘤、恶性神经鞘瘤、粘液瘤有时易混淆，免疫组织化学有助于明确诊断。

Clinical diagnostic considerations ranged from benign entities such as rhabdomyoma, intramuscular lipoma, fibromatosis, myositis ossificans, proliferative myositis, inflammatory myofibroblastic tumor, and inflammatory myopathy to malignant entities such as rhabdomyosarcoma, leiomyosarcoma, liposarcoma, and lymphoma.

这些病例的临床考虑多样，有良性的横纹肌瘤、肌内脂肪瘤、纤维瘤病、骨化性肌炎、增生性肌炎、炎性肌纤维母细胞瘤和炎性肌病，也有恶性的横纹肌肉瘤、平滑肌肉瘤、脂肪肉瘤和淋巴瘤。

Dedifferentiated liposarcoma, occurring in up to 10% of well differentiated liposarcoma cases, has similar histologic features to that of undifferentiated high-grade pleomorphic sarcoma; the former develops in a background of atypical lipomatous tumors/well differentiated liposarcoma, whereas the latter shows no specific line of differentiation.

去分化脂肪肉瘤占高分化脂肪肉瘤比例达10%，其形态特征与未分化高级别多形性肉瘤有相似之处；前者发生在不典型脂肪肿瘤/高分化脂肪肉瘤的背景上，后者无特定分化方向。

We conclude that conventional myxoid liposarcoma is by far the most common subtype of liposarcoma in young patients, with an excellent prognosis.

总结：普通型黏液样脂肪肉瘤是年轻患者的脂肪肉瘤中最常见的一个亚型，且预后极好。

The degree of histolog differentiation and malignancy can be evaluated on the basis of MRI findings of liposarcoma.Key Words Liposarcoma; mRI; Diagnosis

根据脂肪肉瘤的MRI表现，可评估肿瘤的分化和恶性程度。

Thirty-seven of 38 patients with follow-up are alive without disease and 1 is alive with disease (median 59 mo follow-up duration, range: 8 to 108 mo). Six cases showed myxoid liposarcoma with spindled growth (spindle cell myxoid liposarcoma); these arose in 5 females and 1 male (median age 14 y) and involved the thigh in 40% of cases.

随访的38例都存活，其中37例无再发，1例伴病（随访中位时间为59个月，范围：8至108个月）。6例黏液样脂肪肉瘤的瘤细胞生长方式为梭形（梭形细胞黏液样脂肪肉瘤），患者为5名女性、1名男性（中位年龄14岁），40%病例的肿瘤发生于大腿。

As she looked at Warrington's manly face, and dark, melancholy eyes, she had settled in her mind that he must have been the victim of an unhappy attachment.

每逢看到沃林顿那刚毅的脸，那乌黑、忧郁的眼睛，她便会相信，他一定作过不幸的爱情的受害者。

Maybe they'll disappear into a pothole.

也许他们将在壶穴里消失