Dermatofibroma in Adult
Alerts and Notices
SynopsisDermatofibromas (DFs), or fibrous histiocytomas, are common, benign skin neoplasms composed of collagen, macrophages (histiocytes), capillaries, and fibroblasts. The etiopathogenesis is unknown, though some may arise at sites of trauma or insect bites. They are firm, skin-colored, pink, or slightly pigmented papules or nodules. They are usually asymptomatic but may be tender or pruritic, and they often persist for life. They are most common on the legs of women and usually appear in young adulthood. They may eventuate into depressed scars after several years.
DFs are often solitary, though any individual may have more than one. Rarely, multiple eruptive dermatofibromas (MEDFs) may be seen. MEDF is arbitrarily defined as the presence of 5 to 15 or more DFs developing in less than a 4-month period. MEDF has been reported to occur in individuals with HIV infection; autoimmune disease, most frequently systemic lupus erythematosus; neoplastic disease; and in pregnant individuals. Multiple clustered dermatofibroma (MCDF) is a rare entity that develops in the first to third decades, where 15 or more DFs cluster together to form a plaque, most often on the lower half of the body.
In rare families with dominantly inherited DF, missense mutation in the factor XIII A-subunit has been detected.
Some rare variants of DFs, particularly aneurysmal, cellular, and atypical fibrous histiocytomas, are characterized by an increased risk of local recurrence compared to conventional DFs:
- Aneurysmal DF (hemorrhagic or hemosiderotic DF): This variant represents less than 2% of DFs. It mainly arises in young adults and shows rapid growth. Lesions tend to be larger than typical DFs, with a cystic consistency and a pigmented or vascular appearance. The rate of recurrence is about 20% following excision.
- Cellular DF: This variant represents less than 5% of cutaneous fibrous histiocytomas. Although more common in the extremities, it can sometimes occur on the face, ears, hands, and feet. In comparison to common DFs, cellular DFs are larger in size with a predilection for men and a higher recurrence rate of up to 26% in some studies.
- Atypical DF (DF with monster cells): This variant is usually seen in middle-aged adults. Lesions are slightly larger than 1 cm in diameter and are clinically similar to common DFs.
D23.9 – Other benign neoplasm of skin, unspecified
427186000 – Dermatofibroma
Differential Diagnosis & Pitfalls
- Melanocytic nevus
- Blue nevus
- Dysplastic nevus
- Keloid or hypertrophic scar (see scar)
- Prurigo nodularis
- Dermatofibrosarcoma protuberans (DFSP) is a locally invasive malignant neoplasm that can begin as a DF-size lesion. DFSP favors the trunk and progressively increases in size, while DFs do not substantially increase in size and favor the extremities.
- Spitz nevus
- Amelanotic or melanotic melanoma
- Atypical fibroxanthoma
- Neurilemmoma (schwannoma)
- Foreign body granuloma
- Supernumerary nipple
- Lichenoid keratosis
- Basal cell carcinoma
- Inflamed seborrheic keratosis
- Squamous cell carcinoma
- Multinucleated cell angiohistiocytoma
Patient Information for Dermatofibroma in Adult
Dermatofibroma in Adult