A Case of Multiple Angiomyxolipoma / 대한피부과학회지
Korean Journal of Dermatology
; : 1090-1095, 2008.
Article
in Korean
| WPRIM (Western Pacific)
| ID: wpr-50116
Responsible library:
WPRO
ABSTRACT
Angiomyxolipoma is a rare variant of lipoma and seven cases have been reported in the English literature. The reported cases mostly presented with a well-demarcated, asymptomatic, solitary, subcutaneous mass on the scalp or extremities. Histopathologic features of this tumor are characteristic and consist of the paucicellular myxoid areas and the mature fat tissue, with numerous thin, dilated blood vessels. The important histopathological differential diagnoses include myxoid spindle cell lipoma, myxoid lipoma, angiolipoma, angiomyolipoma, superficial angiomyxoma, myxoid liposarcoma and low-grade myxofibrosarcoma. We describe a 38-year-old man with multiple angiomyxolipoma on the gluteal area and the upper and lower extremities.
Full text:
Available
Database:
WPRIM (Western Pacific)
Main subject:
Scalp
/
Blood Vessels
/
Liposarcoma, Myxoid
/
Angiomyolipoma
/
Angiolipoma
/
Lower Extremity
/
Diagnosis, Differential
/
Extremities
/
Lipoma
/
Myxoma
Type of study:
Diagnostic study
Limits:
Adult
/
Humans
Language:
Korean
Journal:
Korean Journal of Dermatology
Year:
2008
Document type:
Article