Results 1 to 10 of about 202,793 (380)

Cytomorphologic Spectrum of SMARCB1-Deficient Soft Tissue Neoplasms. [PDF]

open access: greenAm J Clin Pathol, 2021
Abstract Objectives The SWI/SNF complex core subunit SMARCB1 is inactivated in a variety of neoplasms that share characteristic “rhabdoid” cytomorphology. The aim of this study was to evaluate SMARCB1-deficient soft tissue neoplasms on cytology to identify diagnostic clues.
Schaefer IM, Al-Ibraheemi A, Qian X.
europepmc   +5 more sources

The Rapidly Expanding Group of RB1-Deleted Soft Tissue Tumors: An Updated Review [PDF]

open access: yesDiagnostics, 2021
The classification of soft tissue tumors has evolved considerably in the last decade, largely due to advances in understanding the pathogenetic basis of many of these, sometimes rare, tumors.
Sasha Libbrecht   +2 more
doaj   +3 more sources

Soft tissue neoplasms: a clinicopathological study [PDF]

open access: yesInternational Journal of Research in Medical Sciences, 2020
Background: The current WHO classification has categorized soft tissue tumours into benign, malignant and so-called intermediate neoplasms. Soft tissue sarcoma comprises <1% of adult cancers. The aim of the study was to clinically correlate soft tissue neoplasms and study the histomorphological features of various malignant soft tissue tumors ...
K T Athulya Krishna Kumar, S Ariya
openaire   +4 more sources

A Case Series of Myopericytoma: A Soft Tissue Neoplasm [PDF]

open access: goldNATIONAL JOURNAL OF LABORATORY MEDICINE
Myopericytoma (MPC) is a rare benign mesenchymal neoplasm with perivascular myoid differentiation that most commonly arises in middle adulthood. The lesion generally involves the subcutaneous soft tissue of the lower extremities. Histologically, it is characterised by concentric perivascular proliferation of spindled myoid cells with bland elongated ...
Nupur Kaushik   +3 more
openaire   +3 more sources

Clinicopathological study of soft tissue tumours in a tertiary care hospital in south India [PDF]

open access: yes, 2022
Background: Soft tissue tumours are more diverse and heterogenous group of rare tumours. Soft tissue Sarcomas comprise
M., Prabha, V., Amirtharajan
core   +2 more sources

SOFT TISSUE SARCOMA - SANTA CASA DE SÃO PAULO EXPERIENCE FROM 2006 TO 2019

open access: yesActa Ortopédica Brasileira, 2023
Objective: To conduct an epidemiologic review, analyzing treatment, evolution, and survival of soft tissue sarcomas. Methods: Retrospective study based on medical records of patient with STS treated by the Orthopedic Oncology Group at the Santa Casa ...
BRUNA BUSCHARINO   +5 more
doaj   +1 more source

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