Literature DB >> 8367204

Intra-abdominal desmoplastic small round cell tumor.

G Yeoh1, P Russell, E J Wills, S Fleming.   

Abstract

A rarely encountered but distinctive type of aggressive malignant tumor of childhood and adolescence has been recently described as occurring predominantly or exclusively intrabdominally. It is characterized by a generally diffuse pattern of growth of small cells with hyperchromatic nuclei, scanty cytoplasm, patchy epithelial differentiation, immunohistochemical co-expression of keratin and desmin intermediate filaments and a focal but pronounced desmoplastic stromal component. It is regarded as yet another variant in the group of small round cell tumors (SRCT) of infancy and childhood. This case report of a mass in the greater omentum of a 15 yr-old girl adds to the 33 cases already described in the English literature.

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Year:  1993        PMID: 8367204     DOI: 10.3109/00313029309084800

Source DB:  PubMed          Journal:  Pathology        ISSN: 0031-3025            Impact factor:   5.306


  2 in total

1.  Sister Mary Joseph nodule caused by metastatic desmoplastic small round cell tumor: A clinicopathological report.

Authors:  Noppadol Larbcharoensub; Atcharaporn Pongtippan; Duangjai Pangpunyakulchai; Sith Phongkitkarun; Panuwat Lertsithichai; Thitiya S Dejthevaporn
Journal:  Mol Clin Oncol       Date:  2016-08-24

2.  Is the EWS/FLI-1 fusion transcript specific for Ewing sarcoma and peripheral primitive neuroectodermal tumor? A report of four cases showing this transcript in a wider range of tumor types.

Authors:  P Thorner; J Squire; S Chilton-MacNeil; P Marrano; J Bayani; D Malkin; M Greenberg; A Lorenzana; M Zielenska
Journal:  Am J Pathol       Date:  1996-04       Impact factor: 4.307

  2 in total

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