Fibroma - Related Links
Open Access Articles- Top Results for Fibroma
Journal of SpineSpinal Deformity in Neurofibromatosis: Classification and Management
Oral Health and Dental ManagementA Massive Peripheral Ossifying FibromaUncommon Presentation of a Common Lesion
Journal of Clinical Case ReportsMetastatic Seminoma Presenting as Enlarging Retroperitoneal Mass in a Patient with Neurofibromatosis I
Journal of Genetic Syndromes & Gene TherapyHiding in Plain Sight: A Consideration of NF1-Associated Hypovitaminosis D and its Treatment
Journal of Clinical & Experimental Dermatology ResearchSkin Elasticity in Neurofibromatosis Type 1: Rheological and Histological Analysis
Soft fibroma (fibroma molle)
|Classification and external resources|
Fibromas (or fibroid tumors or fibroids) are benign tumors that are composed of fibrous or connective tissue. They can grow in all organs, arising from mesenchyme tissue. The term "fibroblastic" or "fibromatous" is used to describe tumors of the fibrous connective tissue. When the term fibroma is used without modifier, it is usually considered benign, with the term fibrosarcoma reserved for malignant tumors.
The hard fibroma (fibroma durum) consists of many fibres and few cells, e.g. in skin it is called dermatofibroma (fibroma simplex or nodulus cutaneous). A special form is the keloid, which derives from hyperplastic growth of scars.
The soft fibroma (fibroma molle) or fibroma with a shaft (acrochordon, skin tag, fibroma pendulans) consist of many loosely connected cells and less fibroid tissue. It mostly appears at the neck, armpits or groin. The photo shows a soft fibroma of the eyelid.
Other types of fibroma
The fibroma cavernosum or angiofibroma, consists of many often dilated vessels, it is a vasoactive tumor occurring almost exclusively in adolescent males.
The cystic fibroma (fibroma cysticum) has central softening or dilated lymphatic vessels.
The myxofibroma (fibroma myxomatodes) is produced by liquefaction of the underlying soft tissue.
Other fibromas: chondromyxoid fibroma, desmoplasmic fibroma, nonossifying fibroma, ossifying fibroma, nuchal fibroma, collagenous fibroma, fibroma of tendon sheath, perifollicular fibroma, pleomorphic fibroma, uterine fibroma, etc.
It appears in the sex cord-stromal tumour group of ovarian neoplasms. Ovary fibromas are most frequent during middle age, and rare in children. Upon gross pathological inspection, ovary fibromas are firm and white or tan. Variants with edema are especially likely to be associated with Meigs' syndrome. On microscopic examination, there are intersecting bundles of spindle cells producing collagen.
Benign fibromas can be removed or left alone. Removal is usually a brief outpatient procedure.
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