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ID 62780
JaLCDOI
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75_5_653.pdf 5.34 MB
Author
Tsuchie, Hiroyuki Department of Orthopedic Surgery, Akita University Graduate School of Medicine
Miyakoshi, Naohisa Department of Orthopedic Surgery, Akita University Graduate School of Medicine
Nagasawa, Hiroyuki Department of Orthopedic Surgery, Akita University Graduate School of Medicine
Nanjo, Hiroshi Department of Pathology, Akita University Graduate School of Medicine
Shimada, Yoichi Department of Orthopedic Surgery, Akita University Graduate School of Medicine
Abstract
We present an extremely rare case of deep angiomyxoma (DAM) in the thigh that was misdiagnosed as desmoid-type fibromatosis. A 40-year-old Japanese woman presented with a mass on the left thigh. The histological diagnosis by needle biopsy was desmoid-type fibromatosis; the tumor grew slowly and was resected 4 years later. The histological diagnosis from the resected tumor was DAM. As of 16 months post-surgery, the patient has not noticed any local recurrence. Although DAM in a lower extremity is extremely rare, clinicians must be aware of its possible occurrence in areas relatively close to the pelvis.
Keywords
deep angiomyxoma
thigh
desmoid-type fibromatosis
Amo Type
Case Report
Publication Title
Acta Medica Okayama
Published Date
2021-10
Volume
volume75
Issue
issue5
Publisher
Okayama University Medical School
Start Page
653
End Page
657
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
Copyright Holders
CopyrightⒸ 2021 by Okayama University Medical School
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT
NAID