spindle cell lipoma
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Introduction
part of histologic spectrum of spindle cell lipoma & pleomorphic lipoma.
Epidemiology
- older men, median age over 50 yrs.
- predominantly posterior neck & shoulder
- face, forehead, scalp, buccal-perioral area, upper arm less common; lower extremity rare
Pathology
oval/discoid yellow/gray/white mass, firmer texture than ordinary lipomas
Microscopic pathology
- variable numbers of adipocytes
- bland mitotically inactive spindle cells
- thick rope like collagen bundles
- often large numbers of mast cells
- may show myxoid stromal change or slit like spaces resembling vascular slits
Immunophenotype
CD34 strongly positive S100 may rarely be positive
Genetics
- frequently hypodiploid
- monosomy/partial monosomy 13/16
- breakpoint chromosome 16q13 with loss of 16q13-qter
- chromosome 13q12 and 13q14-q22 losses
Clinical manifestations
- asymptomatic, circumscribed, mobile dermal or subcutaneous mass
- long history
- usually single lesions
Management
- benign behavior
- conservative local excision
More general terms
References
- ↑ WHO Classification Tumours of Soft Tissue and Bone Fletcher, Unni & Mertens Eds. IARC Press 2002