临床鉴别诊断包括骨纤、骨瘤、皮样囊肿、脑膜瘤、嗜酸性肉芽肿、朗格·汉斯组织细胞增生症、以及转移瘤。
Clinical differential diagnosis includes fibrous dysplasia, osteoma, dermoid cyst, meningioma, eosinophilic granuloma, Lagerhan cell histiocytosis, and metastatic disease.
软组织的软骨瘤也会影响手部，但是通常此瘤界限清楚，有很多发育良好的软骨样分化。
Chondroma of soft parts also affects the hands but it is usually well circumscribed and has more well developed chondroid differentiation.
软组织的软骨瘤也会影响手部，但是通常此瘤界限清楚，有很多发育良好的软骨样分化。
Chondroma of soft parts also affects the hands, but it is usually well circumscribed and has more well developed chondroid differentiation.
目的：探讨活动期瘤样钙质沉着症的临床表现、组织病理学改变。
Objective: to investigate the clinical manifestations and histopathologic features of the tumoral calcinosis at active stage.
组织细胞样细胞可演变为泡沫细胞和多核、单核的瘤巨细胞，另见少量未分化间叶细胞。
The histiocyte-like ce- lls may be transformed into foamy cells, mononucleated or multinucleated tumor giant cells. Undifferentiated mesenchymal cells were rarely seen.
肿瘤由形态多样的上皮样细胞构成，胞质嗜酸性或透亮，来源于中间型滋养细胞。免疫组织化学瘤细胞表达CK、MBP、H CG、HPL等。
The tumor cells were composed of polymorphic epithelioid cells with eosinophilic or clear cytoplasm, and they derived from intermediate trophoblast (it), and could expressed CK, MBP, HCG and HPL.
当怀疑脂肪瘤、皮样囊肿、视神经肿瘤管内或颅内蔓延等软组织肿瘤行MRI检查。
If liposarcoma, dermoid cyst, neurotubule tumor or intracranial invasion is suspected, MRI should be highly considered.
目的：观察栅状肌纤维母细胞瘤的临床病理特征，探索该肿瘤的组织来源及石棉样纤维的性质和来源。
Purpose To observe the clinical pathologic characteristics of palisaded myofibroblastoma, approach its histogenesis and the nature of the amianthoid fibers (AF).
横纹肌样瘤通常在肾脏中开始，但它们也可以出现或移动到脑和其他软组织中。
Rhabdoid tumors typically start out in the kidneys, but they can also arise or migrate into the brain and other soft tissues.
结论：肝脏血管周上皮样细胞瘤是一种非常罕见的间叶组织来源肿瘤。
Conclusion: EComa is a very rare tumor of the liver which arises from mesenchymal tissues.
目的：观察皮下脂膜炎样T细胞淋巴瘤(SPTCL)的临床表现并分析SPTCL的病理组织学形态、诊断及鉴别诊断。
Objective to analyzes the histopathological and clinical features for diagnosis of subcutaneous panniculitis like t cell lymphoma (SPTCL).
瘤组织内血管稀少，未见类微血管样结构；
Rarefied vessels were found in tumor, and no vessel like structure formed by tumor cells was observed.
组织学，病变特征性地表现为淋巴样细胞夹杂着大细胞弥漫浸润，高度可疑淋巴瘤。
Histologically, they are characterized by a dense lymphoid infiltrate with admixed large cells that is often suspicious for lymphoma.
组织，膜蛋白，人肿瘤细胞系，A431 （人表皮样畸胎瘤）
Tissue, Membrane Protein, Human Tumor Cell Line, A431 (Human Epidermoid Carcinoma)
瘤组织由梭形细胞和胶原纤维束交织而成，可发生玻璃样变和钙化。
Tumor tissue from the spindle cells and collagen fiber bundles cutting through, glass-like degeneration and calcification.
结果，CFN表达与瘤组织类型有关：上皮型，CFN分布以肾小管样结构周围为主，而且表达强度高；
The results showed that the expression of CFN was correlated with the histological type of the tumor. In epithelial type, CFN distributed around the cell and had a high expression intensity.
受体酪氨酸激酶样孤儿受体1（ROR1）是在B-细胞恶性肿瘤和实体瘤亚群上表达的，但不在健康B细胞或正常产后组织中表达。
Receptor tyrosine kinase-like orphan receptor-1 (ROR1) is expressed on sub-populations of B-cell malignancies and solid tumors, but not by healthy B cells or normal postpartum tissues.
瘤细胞间见多量骨样组织和软骨样组织。
There are lots of osteoid tissue and chondral tissue in the tumor.
瘤组织由梭形细胞和胶原纤维束交织而成，可发生玻璃样变和钙化。
When skin is injured the weave-like structure of collagen fibers, the skin's glue, is destroyed.
组织学上多形T细胞淋巴瘤5例，B细胞淋巴瘤4例，其中淋巴浆细胞样型和小细胞性各2例。
Histologically, 5 of 9 cases were polymorphoral(peripheral) T cell lymphoma, in the rest 4 of B cell lymphoma, 2 were lymphoplasmacytoid and the other 2 were small cell type.
组织学上多形T细胞淋巴瘤5例，B细胞淋巴瘤4例，其中淋巴浆细胞样型和小细胞性各2例。
Histologically, 5 of 9 cases were polymorphoral(peripheral) T cell lymphoma, in the rest 4 of B cell lymphoma, 2 were lymphoplasmacytoid and the other 2 were small cell type.
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