What Causes Plantar Fibroma and Its Key Risk Factors?

Plantar fibroma is a non-cancerous growth on the sole of the foot. This condition can cause discomfort and affect foot function, prompting interest in its origins. This article explores the nature of plantar fibroma and its genetic, cellular, and associated risk factors.

Understanding Plantar Fibroma

Plantar fibroma is a benign nodule or lump forming within the plantar fascia, a thick tissue band along the bottom of the foot. This tissue extends from the heel bone to the toes, supporting the foot’s arch. The nodule consists of an overgrowth of fibrous tissue, primarily involving fibroblasts and excessive collagen. These growths are typically slow-growing, ranging from a small pea to a noticeable mass.

Genetic Predisposition

Genetic background and family history significantly influence plantar fibroma development, with a strong hereditary link observed in affected individuals. Specific genetic variants, including an indel (chr5:118704153:D) and a single nucleotide polymorphism (rs62051384), may increase susceptibility. Plantar fibroma often appears alongside other fibrous overgrowth disorders like Dupuytren’s contracture and Peyronie’s disease, which also have genetic links. These associations suggest a shared underlying genetic predisposition, possibly involving defects in wound repair. The condition is also more common in populations of Northern European descent.

Cellular and Tissue Abnormalities

Plantar fibroma formation involves specific cellular and tissue processes. Fibroblasts, the cells responsible for producing connective tissue components like collagen, become unusually active and proliferate excessively. This leads to an overproduction and accumulation of collagen, particularly type III collagen, and other elements of the extracellular matrix. This uncontrolled growth of fibrous tissue forms the palpable nodule characteristic of plantar fibroma.

The development of these fibromas typically progresses through three stages: a proliferative phase (increased cell numbers), an active phase (nodule formation and increased collagen production), and a residual phase (collagen maturation and potential scarring). While the exact triggers for this cellular overactivity are not fully understood, repetitive microtrauma or chronic irritation to the plantar fascia can initiate or worsen this abnormal cellular response. An increased release of certain growth factors, such as insulin-like growth factor-1, fibroblast growth factor, platelet-derived growth factor, and transforming growth factor-beta, along with elevated interleukins, has been implicated in stimulating this hyperactive fibroblast behavior.

Associated Risk Factors

Beyond genetic and cellular mechanisms, several systemic conditions and external factors increase the likelihood of developing plantar fibroma. Certain medical conditions, including diabetes, epilepsy, chronic liver disease, and thyroid disorders, are linked to a higher incidence of these growths. These conditions may indirectly influence cellular metabolism or connective tissue health, contributing to fibroma formation. Specific medications, such as the anti-seizure drug phenytoin and some beta-blockers, are also potential risk factors.

Chronic alcohol use disorder and smoking are additional factors that increase risk. Plantar fibromas are most commonly observed in middle-aged and older adults, typically appearing between ages 30 and 60. While both men and women can be affected, some studies suggest men are about twice as likely to develop the condition.