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The American Journal of Surgical Pathology, ISSN 0147-5185, 10/2019, Volume 43, Issue 10, pp. 1349 - 1354
Cutaneous syncytial myoepithelioma (CSM) is a rare but distinctive benign variant in the family of myoepithelial neoplasms of skin and soft tissue. CSM has... 
soft tissue | EWSR1 | RNA-Seq | syncytial | PBX3 | skin | myoepithelioma | Index Medicus
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 08/2019
Pericytic tumors comprise a histologic continuum of neoplasms with perivascular myoid differentiation, which includes glomus tumors, myopericytoma, myofibroma,... 
Index Medicus
Journal Article
Skeletal Radiology, ISSN 0364-2348, 03/2019, Volume 48, Issue 3, pp. 437 - 443
Journal Article
2013, 1. Aufl., ISBN 1461450039, Volume 9781461450047, 376
Management of Soft Tissue Sarcoma addresses the diagnosis and best current management of adult soft tissue sarcomas. Edited by world renowned experts, this... 
Clinical & internal medicine | Connective tissues | Sarcoma | Tumors | Soft tissue tumors
eBook
Genes Chromosomes and Cancer, ISSN 1045-2257, 12/2007, Volume 46, Issue 12, pp. 1051 - 1060
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 12/2018, Volume 42, Issue 12, pp. 1653 - 1661
Pseudomyogenic hemangioendothelioma (PHE) is an uncommon, rarely metastasizing vascular neoplasm with predilection to affect young adults. The tumors often... 
FOSB | pseudomyogenic hemangioendothelioma | ACTB | SERPINE1 | SURGERY | NEOPLASM | HEMANGIOMA | HYBRIDIZATION | PATHOLOGY | REARRANGEMENTS | SUBSET | SARCOMA-LIKE HEMANGIOENDOTHELIOMA | T(7/12) | EPITHELIOID SARCOMA | BONE | PERICYTOMA | Hemangioendothelioma | Usage | Young adults | Analysis | Fluorescence in situ hybridization | Genetic aspects | Health aspects | Gene fusion | Index Medicus
Journal Article
The American journal of surgical pathology, ISSN 0147-5185, 06/2015, Volume 39, Issue 6, pp. 871 - 872
Journal Article
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 3358 - 3358
Journal Article
12/2016, Second edition., ISBN 3319419048, 398
Management of Soft Tissue Sarcoma, 2nd Edition provides the most comprehensive analysis of demographics and natural history currently available for these... 
Soft tissue tumors | Clinical & internal medicine | Surgical oncology | Medicine & Public Health | Oncology | Surgical Oncology
eBook
The American Journal of Surgical Pathology, ISSN 0147-5185, 10/2019, Volume 43, Issue 10, pp. 1384 - 1391
A major breakthrough in the classification of soft tissue tumors has been the recent identification of NTRK-fusion related neoplasms which are amenable to... 
Index Medicus
Journal Article
Journal Article
Genes, Chromosomes and Cancer, ISSN 1045-2257, 04/2016, Volume 55, Issue 4, pp. 291 - 310
Journal Article
Modern Pathology, ISSN 0893-3952, 2019
GLI1 fusions involving ACTB, MALAT1, and PTCH1 genes have been recently reported in a subset of malignant soft tissue tumors with characteristic monomorphic... 
Journal Article
Genes Chromosomes & Cancer, ISSN 1045-2257, 09/2017, Volume 56, Issue 9, p. 663
An increasing number of congenital and infantile sarcomas displaying a primitive, monomorphic spindle cell phenotype have been characterized to harbor... 
Journal Article
The American Journal of Surgical Pathology, ISSN 0147-5185, 04/2018, Volume 42, Issue 4, pp. 553 - 560
Journal Article
Genes, chromosomes & cancer, ISSN 1045-2257, 2/2018, Volume 57, Issue 2, pp. 89 - 95
Poorly differentiated chordomas (PDCs) represent a rare subset of notochordal neoplasms, affecting primarily children and associated with an aggressive... 
Brachyury | Chordoma | SMARCB1 | Poorly differentiated chordoma | INI1
Journal Article
The American journal of surgical pathology, ISSN 0147-5185, 4/2018, Volume 42, Issue 4, pp. 553 - 560
ACTB1-GLI1 fusions have been reported as the pathognomonic genetic abnormality defining an unusual subset of actin-positive, perivascular myoid tumors, known... 
SHH | S100 protein | pericytoma | PTCH1 | gastroblastoma | MALAT1 | GLI1 | ACTB
Journal Article
Journal Article
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