Hidradenitis suppurativa

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Hidradenitis suppurativa
Hidradenitis suppurativa (stage II) in axilla.jpg
Hidradenitis suppurativa (stage II) in the left armpit
Synonyms Acne inversa, acne conglobata,
apocrine acne, Verneuil's disease, Velpeau’s disease


Specialty Dermatology
Symptoms Multiple inflamed and swollen skin lesions


Usual onset Young adulthood
Duration Long-term
Types Stage I, II, III
Causes Unknown


Diagnosis Based on symptoms
Differential diagnosis Acne, acne conglobata, pilonidal cysts


Treatment Warm baths, laser therapy, surgery
Medication Antibiotics, immunosuppressive medication


Frequency 1–4% of people
Deaths Rare

Hidradenitis suppurativa (HS), alternatively known as acne inversa, is a chronic skin disease manifested by recurrent inflamed lesions and nodules. These lesions are frequently painful and prone to rupture, releasing fluid or pus. Scar tissue often forms after the lesions heal. Due to its physical manifestations, HS can have significant psychosocial impacts, including self-consciousness and depression.

Presentation and Affected Areas[edit]

HS typically manifests in areas of the body where skin rubs together, like the axillary (underarm) regions, inframammary (under the breasts) areas, and the groin. Lesions may also develop around the anal and genital areas. The skin condition evolves from small, pimple-like bumps to hard, painful nodules that can persist for weeks or months.

Etiology[edit]

The precise etiology of HS remains uncertain, but it's thought to arise from a combination of genetic predispositions and environmental triggers. Approximately one-third of HS patients have a family history of the disease. Modifiable risk factors, such as obesity and smoking, are also associated with HS. The condition is not infectious, and it does not result from poor hygiene or deodorant use.

The pathogenesis is believed to involve either apocrine sweat gland dysfunction or hair follicle abnormalities, leading to follicular occlusion and secondary bacterial infection and inflammation.

Diagnosis[edit]

Diagnosis of HS is primarily clinical, based on characteristic patient history and physical examination. The recurrent nature of the painful, pus-filled nodules in the characteristic body areas strongly points to this condition.

Treatment[edit]

Management of HS focuses on reducing flare-ups, relieving symptoms, and preventing disease progression. It often involves a combination of lifestyle modifications, medications, and in severe cases, surgical intervention.

References[edit]


See also[edit]

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