eMedicine Specialties > Dermatology > Benign Neoplasms
Elastofibroma: Differential Diagnoses & Workup
Updated: Jul 21, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
Differential Diagnoses
Other Problems to Be Considered
Extra-abdominal fibromatosis
Sarcoma
Subcutaneous metastasis
Lipoma17
Workup
Imaging Studies
- Elastofibromas have a typical sonographic appearance consisting of arrays of linear strands against an echogenic background.18 However, in some cases, the ultrasound pattern of an elastofibroma dorsi may be very similar to the surrounding muscular tissue, and neither a clear cleavage surface nor a specific vascular pattern can be seen. In these cases, the elastofibroma may be very difficult to distinguish from surrounding tissue.19
- Chest wall radiographic findings are usually normal; however, elevation of the scapula from the chest wall has been detected in a few cases.20
- CT scanning and MRI reveal a lenticular, unencapsulated, soft tissue mass with skeletal muscle attenuation interspersed with strands of fat attenuation.21,22,23 Small elastofibromas may be difficult to visualize on CT scans or MRIs, but they can be enhanced by the use of gadolinium. Its characteristic location (periscapular region) and specific imaging appearance on ultrasound images, CT scans, and MRIs facilitates accurate diagnosis.24 Noninvasive techniques, especially MRI, and histologic assessment are closely correlated, so that sometimes a biopsy can be avoided.25
- Incidental detection of bilateral elastofibroma dorsi with F-18 fluorodeoxyglucose positron emission computed tomography scanning has been described.26
Procedures
- A biopsy specimen should be obtained from the affected area. The surgical excision should be large and should include skin, subcutaneous fatty tissue, and, if necessary, deeper tissue. A shave or punch biopsy is not sufficient.
Histologic Findings
The tumor grossly appears as an ill-defined mass with a white or gray-white, glistening surface.
Upon light microscopy, elastofibromas are dermal unencapsulated tumors composed of branched and unbranched elastic fibers, eosinophilic collagen bundles, and scattered fatty tissue. The elastic fibers have a degenerated, beaded appearance or are fragmented into small globules or droplets arranged in a linear pattern. The epidermis is usually unaffected. The interspersed spindle or stellate cells show a fibroblastlike appearance and were almost consistently positive for vimentin and frequently positive for CD34 and lysozyme immunohistochemically.2 The CD105-positive vessels in elastofibromas appear to reflect active neovascularization.27
At an ultrastructural level, the elastic fibers appear as an irregular granular or fibrillary aggregation of electron-dense, amorphous material surrounded by microfibrils and collagen fibers. Collagen fibers are commonly incorporated within the elastic material.
Immunohistochemically, elastofibromas stain positively for vimentin but negatively for smooth muscle actin, S-100, desmin, and p53.28
Because of their densely fibrous nature, hypocellularity may be observed in fine-needle aspiration biopsy specimens of elastofibromas; thus, diagnostic material may be overlooked. The smears show evidence of mature adipocytes, fibroblasts, collagen fibers, globular bodies, and characteristic braidlike or fernlike structures, revealing degenerative elastic fibers. Careful evaluation of the background of the smears coupled with full knowledge of the clinical and radiological findings, including those from MRIs, is required to establish the correct diagnosis; therefore, a skin biopsy is preferable.
More on Elastofibroma |
| Overview: Elastofibroma |
Differential Diagnoses & Workup: Elastofibroma |
| Treatment & Medication: Elastofibroma |
| Follow-up: Elastofibroma |
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References
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Further Reading
Keywords
elastofibroma, elastofibroma dorsi, connective-tissue tumor, connective tissue tumor, elastogenesis
Differential Diagnoses & Workup: Elastofibroma