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The pathological outcomes were as following: pulmonary blastoma in 6, leiomyosarcoma in 3, fibrosarcoma in 2, carcinosarcoma in 2, and pantmorphic sarcoma in 1 patient.
术后病理诊断:肺母细胞瘤6例,平滑肌肉瘤3例,纤维肉瘤2例,癌肉瘤2例(胶冻样物质癌肉瘤1例,结节状癌肉瘤1例),伴有巨细胞的未分化多形性肉瘤1例。
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Spindle cell sarcomas, such as malignant fibrous histocytoma, fibrosarcoma, and leiomyosarcoma.
梭形细胞肉瘤,如恶性纤维组织细胞瘤,纤维肉瘤,平滑肌肉瘤。
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Methods : From July 2003 to November 2007, 21 cases of sarcoma and SC Cancerous ulcer patients were treated, among which 11 cases male and 10 cases female, the age 14~83 (average 50 years old) and upper limb 6 cases and lower limb 15 cases; The pathologic diagnosis is: SC 6 cases, synovial sarcoma 4 cases, malignant fibrohistiocytoma 3 cases, adipose sarcoma 2 cases, osteogenic sarcoma 2 cases, malignant melanoma 2 cases, sarcoma epithelioides 1 case, derma-eminence fibrosarcoma 1 case.
自2003年7月~2007年11月治疗21例肉瘤及鳞癌性溃疡患者,男性11例,女性10例,年龄14~83(平均50岁)。上肢6例,下肢15例;病理为:鳞癌6例,滑膜肉瘤4例,恶性纤维组织细胞瘤3例,脂肪肉瘤2例,骨肉瘤2例,恶性黑色素瘤2例,上皮样肉瘤1例,皮肤隆突性纤维肉瘤1例。
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The sarcomatoid areas generally show features of MFH, fibrosarcoma, or undifferentiated spindle cell sarcoma.
肉瘤样区域可具有恶性纤维组织细胞瘤(malignant fibrohistiocytoma,MFH)、纤维肉瘤或未分化梭形细胞肉瘤的一般特征。
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The malignant tumors included osteogenic osteosarcoma,metastasis tumor(six patients,two with pathologic fractures),chondrosarcoma,malignant fibrous histiocytoma (three patients,one with pathologic fracture),fibrosarcoma,and solitary myeloma.all patients received limb savage procedure with custom knee prosthesis including sevnteen cases of hinge joint and twentyone cases of posterior stability joints.
回顾分析我院接受定制型人工关节置换进行保肢治疗的股骨远端肿瘤患者38 例,其中良性肿瘤9 例,分别是骨巨细胞瘤7例(复发性骨巨细胞瘤5 例,骨折2例),骨巨细胞瘤合并动脉瘤样骨囊肿1 例,骨母细胞瘤1 例;恶性肿瘤29 例,分别是成骨性骨肉瘤16 例,转移性肿瘤6例(骨折2例),软骨肉瘤2 例,恶性纤维组织细胞瘤3例(骨折1例),纤维肉瘤1 例,局灶性骨髓瘤1 例。
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Methods Nuclear β-catenin expression was detected by immunohistochemistry in 77 lesions with desmoid-type fibromatosis and 171 other spindle cell lesions, including superficial fibrmoatosis (n=18), nodular fasciitis (n=36), keloid (n=16), scar (n=10), granulation tissue (n=9), synovial sarcoma (n=38), neufibroma (n=13), solitary fibrous tumor (n=12), gastrointestinal stromal tumor (n=10), low-grade myxofibrosarcoma (n=3), low-grade fibromyxoid sarcoma (n=3), and smooth muscle tumor (n=10). In addition, the immunohistochemical expressions of ER-α, ER-β and Ki-67 were examined in all of the lesions with desmoid-type fibromatosis. The nuclear immunohistochemical staining for nuclear βcatenin and ER-β was graded as high level (≥25% of cells), low level (5%-25%) or none.
采用免疫组织化学染色法检测77例韧带样型纤维瘤病和171例其它良、恶性梭形细胞病变(包括结节性筋膜炎36例、浅部纤维瘤病11例、瘢痕疙瘩16例、增生性瘢痕10例、肉芽组织9例、滑膜肉瘤38例、神经纤维瘤13例、孤立性纤维性肿瘤12例、胃肠间质肿瘤10例、低度恶性黏液纤维肉瘤3例、低度恶性纤维黏液样肉瘤3例及平滑肌肿瘤10例)组织中β-catenin核阳性的表达,同时检测韧带样型纤维瘤病中ER-α、ER-β和Ki-67的表达。
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Results Among the 52 cases, 30 cases were confirmed to fibrosarcomas, which were identical with primary dingnoses;22 cases were revised to malignant fibrous histocytoma (8 cases), malignant nerve sheath tumor (4 cases), monophasic spindle cell synovial sarcoma (3 cases), leiomyosarcoma(3 cases), rhabdomyosarcoma(2 cases) and abdominal desmmoid tumor (2 cases). Of the 18 cases, only two cases were misdiagnosed and were revised to malignant fibrous histocytoma and spindle cell synovial sarcoma, respectively.
结果:1980年前52例中维持原诊断30例,修改诊断22例(42.3%),分别为恶性纤维组织细胞瘤8例、恶性神经鞘膜瘤4例、单相性梭形细胞滑膜肉瘤3例、平滑肌肉瘤3例、横纹肌肉瘤2例、韧带状纤维瘤2例;1980年后纤维肉瘤18例中,维持原诊断16例,修改诊断2例(11.1%),分别为恶性纤维组织细胞瘤和滑膜肉瘤各1例。
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In part Ⅲ of this ariticle,The authors report some other neoplasms and precancerous changes, and they are adenoma of stomach, hemangiofibroma of ovary,carcinoma of Fallopian tube, osteo-petrosis,cholangiocarcinoma, polyps, leukoplakia,atypical hyperplasia, papillar...
这些肿瘤是鼻咽癌、副鼻窦癌、鼻腔癌、食管癌、卵巢癌,淋巴细胞性白血病、白色肉瘸、淋巴肉瘤,外阴癌、纤维肉瘤、原发性肝癌、小肠癌、结肠癌、乳腺癌,圆形细胞肉瘤、纤维瘤、脂肪瘤、马立克氏病、肾癌、畸胎瘤、膀胱乳头状瘤和口腔癌。
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No matter what kinds of sarcomatous elements are found in a retroperitoneal dedifferentiated liposarcoma, its clinical behavior is not the same as high grade fibrosarcomas, leiomyosarcomas, osteosarcomas, chondrosarcomas, rhabdomyosarcomas, or MPNST.
无论在腹膜后去分化型脂肪肉瘤中发现何种类型的其他肉瘤成分,它的临床行为都与高级别纤维肉瘤、平滑肌肉瘤、骨肉瘤、软骨肉瘤、或恶性外周神经鞘膜瘤不同。
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Most of these non-lipogenic elements appear like fibrosarcoma or MFH, and often display features of high grade sarcoma. Sometimes, the sarcomatous elements are that of a low grade fibrosarcoma (consisting exclusively of spindled cells).
大部分非脂肪肉瘤成分镜下很像纤维肉瘤或恶性纤维组织细胞瘤,并且通常显示的是高级别肉瘤的特征。
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fibrosarcoma:纤维肉瘤
1.纤维肉瘤 纤维肉瘤(fibrosarcoma)起源于成纤维细胞,是纤维组织的恶性肿瘤,多见于5岁以下,有些患儿出生时即发现,也称"先天性及婴儿纤维肉瘤",男孩略多于女孩.
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fibrosarcoma:纤维组织: 纤维肉瘤
fetoprotein; AFP 胎蛋白 | fibrosarcoma 纤维组织: 纤维肉瘤 | FIGO: International Federation of Gynecology and Obstetrics 国际妇产科学联盟
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fibrosarcoma:纤维肉瘤 (名)
fibroplasia 纤维素增生 (名) | fibrosarcoma 纤维肉瘤 (名) | fibrositis 纤维组织炎 (名)
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Osteoid fibrosarcoma:骨样纤维肉瘤
Osteoid chondroma 骨软骨瘤 | Osteoid fibrosarcoma 骨样纤维肉瘤 | Osteoid sarcoma 骨样肉瘤
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fibrosarcoma of ear:耳纤维肉瘤
fibrosarcoma of chest wall 胸壁纤维肉瘤 | fibrosarcoma of ear 耳纤维肉瘤 | fibrosis of mediastinum 纵隔纤维化
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fibrosarcoma of bladder:膀胱纤维肉瘤
fibroplastic proliferation 纤维组织增生 | fibrosarcoma of bladder 膀胱纤维肉瘤 | fibrosarcoma of bone 骨纤维肉瘤
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Giant-celled fibrosarcoma; Giant-cell tumor:巨细胞纤维肉瘤
Giant-celled cancer 巨细胞癌 | Giant-celled fibrosarcoma; Giant-cell tumor 巨细胞纤维肉瘤 | Gingival cancer; Carcinoma of gums 齿龈癌
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Osteoid sarcoma:骨样肉瘤
Osteoid fibrosarcoma 骨样纤维肉瘤 | Osteoid sarcoma 骨样肉瘤 | Osteoid tumor 类骨质瘤
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Fibrous sarcoma; Fibroplastic sarcoma:纤维肉瘤
Fibrous rhabdomyoma 纤维横纹肌瘤 | Fibrous sarcoma; Fibroplastic sarcoma 纤维肉瘤 | Fibrous tubercle 纤维性结核节
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myxofibrosarcoma:粘液纤维肉瘤 粘液纤维肉瘤
myxofibromata 粘液纤维瘤 | myxofibrosarcoma 粘液纤维肉瘤 粘液纤维肉瘤 | myxoflagellate 粘鞭毛虫