has_disease_location
neuroblastic tumor
神经母细胞性肿瘤
Ewings sarcoma-primitive neuroectodermal tumor (PNET)
尤文氏肉瘤-原始神经外胚层肿瘤（PNET）
neuroblastoma
神经母细胞瘤
(Neuroblastoma NOS) or (sympathicoblastoma)
A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome (MeSH).
A common neoplasm of early childhood arising from neural crest cells in the sympathetic nervous system, and characterized by diverse clinical behavior, ranging from spontaneous remission to rapid metastatic progression and death. This tumor is the most common intraabdominal malignancy of childhood, but it may also arise from thorax, neck, or rarely occur in the central nervous system. Histologic features include uniform round cells with hyperchromatic nuclei arranged in nests and separated by fibrovascular septa. Neuroblastomas may be associated with the opsoclonus-myoclonus syndrome. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2099-2101; Curr Opin Oncol 1998 Jan;10(1):43-51)
A neuroblastic tumor characterized by the presence of neuroblastic cells, the absence of ganglion cells, and the absence of a prominent Schwannian stroma formation.
Central neuroblastoma
DOID:769
GeneRIF:11705866
GeneRIF:11737230
GeneRIF:11744098
GeneRIF:11782392
GeneRIF:11807986
GeneRIF:11836564
GeneRIF:11859407
GeneRIF:11861392
GeneRIF:11870543
GeneRIF:11877670
GeneRIF:11877677
GeneRIF:11881792
GeneRIF:11928813
GeneRIF:12031683
GeneRIF:12085233
GeneRIF:12118090
GeneRIF:12154078
GeneRIF:12163469
GeneRIF:12174591
GeneRIF:12185581
GeneRIF:12209604
GeneRIF:12239177
GeneRIF:12438307
GeneRIF:12545167
GeneRIF:12557224
GeneRIF:12576454
GeneRIF:12593854
GeneRIF:12598334
GeneRIF:12629151
GeneRIF:12629521
GeneRIF:12647219
GeneRIF:12672031
GeneRIF:12675130
GeneRIF:12717420
GeneRIF:12808116
GeneRIF:12829373
GeneRIF:12884264
GeneRIF:12888911
GeneRIF:12907629
GeneRIF:12916719
GeneRIF:12962147
GeneRIF:12964007
GeneRIF:13679866
GeneRIF:14645238
GeneRIF:14654552
GeneRIF:14663483
GeneRIF:14719101
GeneRIF:14724587
GeneRIF:14745549
GeneRIF:14988008
GeneRIF:14995074
GeneRIF:15004408
GeneRIF:15015775
GeneRIF:15024693
GeneRIF:15083193
GeneRIF:15117961
GeneRIF:15136145
GeneRIF:15166121
GeneRIF:15168079
GeneRIF:15218241
GeneRIF:15240516
GeneRIF:15280446
GeneRIF:15316056
GeneRIF:15322424
GeneRIF:15328517
GeneRIF:15375504
GeneRIF:15448191
GeneRIF:15486895
GeneRIF:15488758
GeneRIF:15514946
GeneRIF:15516980
GeneRIF:15518890
GeneRIF:15547663
GeneRIF:15607966
GeneRIF:15618969
GeneRIF:15644444
GeneRIF:15650242
GeneRIF:15719172
GeneRIF:15735700
GeneRIF:15741235
GeneRIF:15827327
GeneRIF:15849504
GeneRIF:15882878
GeneRIF:15930276
GeneRIF:15994346
GeneRIF:15998644
GeneRIF:16007146
GeneRIF:16051641
GeneRIF:16091745
GeneRIF:16092940
GeneRIF:16098972
GeneRIF:16125842
GeneRIF:16166307
GeneRIF:16177824
GeneRIF:16228012
GeneRIF:16232196
James Malone
MSH:D009447
NB - Neuroblastoma
NCIt:C3270
NIFSTD:birnlex_12631
Neuroblastoma (Schwannian Stroma-Poor)
Neuroblastoma, NOS
Neuroblastomas
SNOMEDCT:269507008
SNOMEDCT:87364003
Sympathicoblastoma
Tomasz Adamusiak
URI: http://www.ebi.ac.uk/cellline#neuroblastoma
[M]Neuroblastoma NOS
[M]Neuroblastoma NOS (morphologic abnormality)
neuroblastoma
neuroblastoma (morphologic abnormality)
neuroblastoma NOS (morphologic abnormality)
NB-神经母细胞瘤
[M]神经母细胞瘤NOS
[M]神经母细胞瘤NOS（形态异常）
中枢神经母细胞瘤
成交感神经细胞瘤
成神经细胞瘤（形态异常）
早产儿常见的肿瘤来源于交感神经系统的神经嵴细胞，具有不同的临床表现，从自发缓解到快速转移进展和死亡。这种肿瘤是儿童时期最常见的腹腔内恶性肿瘤，但也可能起源于胸部，颈部或罕见的中枢神经系统。组织学特征包括均匀的圆形细胞，在巢中排列有多色核，并通过纤维血管间隔分开。神经母细胞瘤可能与眼球阵挛-肌阵挛综合征（MeSH）有关。
早产儿常见的肿瘤来源于交感神经系统的神经嵴细胞，具有不同的临床表现，从自发缓解到快速转移进展和死亡。这种肿瘤是儿童时期最常见的腹腔内恶性肿瘤，但也可能起源于胸部，颈部或罕见的中枢神经系统。组织学特征包括均匀的圆形细胞，在巢中排列有多色核，并通过纤维血管间隔分开。神经母细胞瘤可能与眼球阵挛-肌阵挛综合征（MeSH）有关。（DeVita等人，Cancer：Principles and Practice of Oncology，5th ed，pp2099-2101; Curr Opin Oncol 1998 Jan; 10（1）：43-51）
神经母细胞瘤
神经母细胞瘤 (Schwannian Stroma-Poor)
神经母细胞瘤(Neuroblastomas)
神经母细胞瘤NOS（形态异常）
神经母细胞瘤的特征是神经母细胞的出现，神经节细胞的缺失以及没有明显的Schwannian基质形成。
神经母细胞瘤，NOS
（成神经细胞瘤NOS）或（交感神经细胞瘤）
sympathetic nervous system
交感神经系统