blastemal


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blas·te·ma

 (blă-stē′mə)
n. pl. blas·te·mas or blas·te·ma·ta (-mə-tə)
1. A mass of undifferentiated cells from which an organ or a body part develops, either in normal development or in the regeneration of a lost body part.
2. A structureless substance from which it was formerly believed that cells are formed.

[Greek blastēma, offspring, sprout, from blastos, bud.]

blas·te′mal, blas′te·mat′ic (blăs′tə-măt′ĭk), blas·te′mic (blă-stē′mĭk) adj.
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

blastemal

(blæˈstiːməl) or

blastematic

adj
(Biology) of or relating to blastema
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014
ThesaurusAntonymsRelated WordsSynonymsLegend:
Adj.1.blastemal - of or relating to blastemata
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
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References in periodicals archive ?
[19] The classic triphasic histology consisting of blastemal, epithelial and mesenchymal component were observed in 61.1% of cases.
The group of SBRCT consists of numerous morphologically similar tumors including ES, rhabdomyosarcoma (RMS), neuroblastoma, small-cell osteosarcoma, lymphoblastic lymphoma (LBL),[5] poorly differentiated synovial sarcomas (PDSS), desmoplastic round cell tumor (DRCT), mesenchymal chondrosarcoma (MCS), and blastemal predominant Wilms' tumor (WT).[6] These tumors make the diagnosis difficult because they may be histopathologically indistinguishable, particularly when poorly differentiated or in a small specimen of biopsy.
She underwent a right nephrectomy, and pathology reports identified a tumor measuring 9.2 x 7.0 x 6.5 cm with blastemal, tubular, and mesenchymal components confined to the kidney.
While differential diagnosis included a blastemal predominant Wilms Tumor and congenital mesoblastic nephroma, the tumor was determined to be most consistent with a rare ossifying renal tumor of infancy.
Obtained blastemal samples were fixed in six different freshly prepared fixative solutions according to manufacturer's protocols (Suvarna et al., 2013).
Acinar differentiation, which is the most common, results in trypsin, chymotrypsin, lipase, and BCL10 positivity, making distinction from ACC challenging unless one identifies pathognomonic squamoid morules, and even primitive (blastemal) elements.
The cellular origin of blastemal cells, mechanisms of cellular release from mature tissue, dedifferentiation, accumulation of cells, blastema growth, and tissue patterning have all been the focus of extensive investigations.
Histopathological analysis revealed tumors with characteristics of nephroblastoma, presenting the classical triphasic histology, comprising the blastemal tissue, hyperchromatic nuclei cells with scanty cytoplasm, primitive tubules, and glomeruli formation admixed with mesenchymal and epithelial cells (Figure 3).
All tumors were identified and categorized into blastemal, epithelial, stromal, mixed type, and anaplasia by pathologist after excision, according to National Wilms' Tumor Study (NWTS).
Pathologically, Classical Wilms' tumour has triphasic histology, with components of blastemal, epithelial, and stromal structures, as found in our case.
Igf2 mRNA has been shown to be expressed in blastemal cells of the nephrogenic zone and in interstitial cells of the medullary region, and IGF2 has been shown to be involved in human renal development (7).