1983
DOI: 10.1001/archopht.1983.01040010255015
|View full text |Cite
|
Sign up to set email alerts
|

Juvenile Fibrosarcoma of the Orbit and Eyelid

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

2
2
0

Year Published

1988
1988
2019
2019

Publication Types

Select...
5
3
1

Relationship

0
9

Authors

Journals

citations
Cited by 38 publications
(4 citation statements)
references
References 18 publications
2
2
0
Order By: Relevance
“…Although fibrosarcomas are more likely to be hypercellular with a characteristic herringbone pattern (Fig 16d), to have infiltrating margins, and to have higher mitotic activity, their histologic appearance overlaps too much with that of infantile fibromatosis to allow prediction of the behavior of an individual tumor based on histologic characteristics alone. In fact, some authors believe that in infants the only reliable diagnostic criterion for malignancy is the presence of metastases (43)(44)(45)47,48). …”
Section: Pathologic Featuresmentioning
confidence: 43%
“…Although fibrosarcomas are more likely to be hypercellular with a characteristic herringbone pattern (Fig 16d), to have infiltrating margins, and to have higher mitotic activity, their histologic appearance overlaps too much with that of infantile fibromatosis to allow prediction of the behavior of an individual tumor based on histologic characteristics alone. In fact, some authors believe that in infants the only reliable diagnostic criterion for malignancy is the presence of metastases (43)(44)(45)47,48). …”
Section: Pathologic Featuresmentioning
confidence: 43%
“…The tumor principally involves the extremities, trunk, head, and neck regions and has also been documented at unusual locations, including the retroperitoneum, mesentery, orbit, and ovary [9,10]. More recent articles document the occurrence of congenital gastrointestinal fibrosarcomas involving the duodenum, jejunum, and colon, most often presenting with bowel perforation [2,4,5].…”
Section: Discussionsupporting
confidence: 41%
“…The tumor principally involves the extremities, trunk, head, and neck regions and has also been documented at unusual locations, including the retroperitoneum, mesentery, orbit, and ovary [9,10]. More recent articles document the occurrence of congenital gastrointestinal fibrosarcomas involving the duodenum, jejunum, and colon, most often presenting with bowel perforation [2,4,5].…”
Section: Discussionsupporting
confidence: 41%