2013
DOI: 10.1016/j.prp.2012.10.015
|View full text |Cite
|
Sign up to set email alerts
|

Paratesticular myxoid/round cell liposarcoma harboring type 3 DDIT3-FUS fusion gene: Report of a very rare case

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
2
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
3
2

Relationship

0
5

Authors

Journals

citations
Cited by 7 publications
(2 citation statements)
references
References 12 publications
0
2
0
Order By: Relevance
“…In comparison with well‐differentiated and dedifferentiated liposarcoma, it occurs in a younger age group and arises particularly in the lower extremities (thigh and popliteal area) and very rarely in the abdominal cavity and retroperitoneum. A molecular genetic profile is very helpful with the diagnosis, with the typical t(12;16)(q13.3;p11.2) and t(12;22)(q13.3;q12.2) translocations resulting in human FUS/DDiT3 being found in the majority of cases…”
Section: Fna Diagnostic Aspects Combined With Molecular Informationmentioning
confidence: 99%
See 1 more Smart Citation
“…In comparison with well‐differentiated and dedifferentiated liposarcoma, it occurs in a younger age group and arises particularly in the lower extremities (thigh and popliteal area) and very rarely in the abdominal cavity and retroperitoneum. A molecular genetic profile is very helpful with the diagnosis, with the typical t(12;16)(q13.3;p11.2) and t(12;22)(q13.3;q12.2) translocations resulting in human FUS/DDiT3 being found in the majority of cases…”
Section: Fna Diagnostic Aspects Combined With Molecular Informationmentioning
confidence: 99%
“…In comparison with well-differentiated and dedifferentiated liposarcoma, it occurs in a younger age group and arises particularly in the lower extremities (thigh and popliteal area) and very rarely in the abdominal cavity and retroperitoneum. A molecular genetic profile is very helpful with the diagnosis, 33 with the typical t(12;16)(q13.3;p11.2) and t(12;22)(q13.3;q12.2) translocations resulting in human FUS/DDiT3 being found in the majority of cases. 34,35 Myxofibrosarcoma is constantly cytologically composed of isolated and regular clusters of wavy spindleshaped cells, round cells without a specific pattern, moderate cytonuclear atypia, and an abundant myxoid background as well as curvilinear vascular structures.…”
Section: Myxoid Tumorsmentioning
confidence: 99%