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An 80-year-old man with COVID-19 also had constrictive pericarditis, possibly due to an autoimmune or immunoglobulin related disease, and improved after surgery.

Histopathology is not reliable for detecting early fibrosis in traction alopecia or for showing how severe it is.

The model helps test drugs for clubfoot fibrosis by mimicking cell environments and shows minoxidil reduces harmful collagen links.

A 36-year-old man had unusual skin lesions on his face without hair loss.

Understanding the nanoscale structure of skin fibrosis can improve knowledge of wound healing and tissue regeneration.

The Wnt1/βcatenin pathway is crucial for heart repair after injury.

The conclusion is that fat tissue in the skin is a new finding in Frontal fibrosing alopecia and may contribute to hair follicle and muscle degeneration.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

Fibroblasts are crucial in scar formation and wound healing, with potential therapies aiming for scarless healing.

CD19-CAR T cell therapy may help regenerate skin in systemic sclerosis.

Nerve fibers may worsen mast cell activity, leading to abnormal elastic fiber buildup from sun exposure.

Accurate diagnosis of EFFC is crucial for effective counseling and cosmetic care.

A 46-year-old man was diagnosed with frontal fibrosing alopecia, a condition usually seen in postmenopausal women.

Red dots on the upper chest may be an early sign of certain types of hair loss.

A rare ear cyst contained hair fragments.

Frontal fibrosing alopecia causes hair loss at the front hairline, and no effective treatment exists.

Fibroblasts, cells usually linked to tissue repair, also help regenerate various organs and their ability decreases with age. Turning adult fibroblasts back to a younger state could be a new treatment approach.

Combining anti-androgenic, anti-inflammatory, and anti-fibrotic treatments may improve hair loss outcomes.

Hair follicles respond differently to pulling forces in various regions.

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

Fibroblasts change rapidly during wound healing, forming temporary niches before stabilizing into distinct scar layers.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

A rare skin condition causes red, dark, bumpy facial lesions.

Androgen hormones cause hair follicle scarring in hair loss, and finasteride helps reduce it.

EMT plays a key role in skin fibrosis and offers new therapy targets.

Removing SIX1 in fat cells reduces skin fibrosis.

CTHRC1 is essential for healing and preventing heart rupture after a heart attack.

CCCA is a common, scarring hair loss in Black women that needs early detection.

An 8-year-old boy with hair loss had hair regrowth and responded well to clobetasol propionate treatment.