Plate 07

Hidradenitis Suppurativa

Also called: Acne inversa · Verneuil disease

Follicular & facial
Illustration © Roxana Barin Click to enlarge

General information

  • Chronic, recurrent inflammatory disease of the hair follicle characterized by nodules, abscesses, draining tunnels, and scarring in intertriginous areas.
  • Predominantly affects the axillary, inguinal, genital/perineal, gluteal, and inframammary regions.
  • Pathogenesis primarily involves follicular occlusion, followed by follicular rupture and an intense inflammatory response; HS is not primarily a disorder of apocrine gland obstruction.
  • Usually begins after puberty, commonly in young adulthood.
  • More common in women.
  • A family history is present in a substantial subset of patients.
  • Strongly associated with smoking and obesity.
  • May be associated with metabolic syndrome, severe acne, pilonidal disease, and inflammatory bowel disease.
  • Secondary bacterial infection may occur, but HS is not primarily an infectious disease.
  • Can have a profound impact on pain, mobility, sexual health, and quality of life.

Symptoms / presentation

  • Recurrent, painful, deep inflammatory nodules.
  • Abscesses may rupture and produce purulent or seropurulent drainage, which may be malodorous.
  • Lesions characteristically recur at the same anatomical sites.
  • Chronic disease may lead to subcutaneous tunnels (sinus tracts) and permanent scarring.
  • Characteristic double-ended or polyporous comedones.
  • Pain may be severe or throbbing.
  • Diagnosis is supported by the triad of typical lesions + typical distribution + chronicity/recurrence.

Clinical exam

  • Deep, tender inflammatory nodules.
  • Deep abscesses.
  • Purulent or seropurulent drainage may be present.
  • Subcutaneous tunnels / sinus tracts in chronic disease.
  • Double-ended comedones +++, a characteristic finding.
  • Nodules may coalesce into indurated plaques or masses.
  • Hypertrophic, fibrotic, or bridging scars.
  • Advanced disease may cause extensive architectural distortion and functional impairment.

HURLEY CLASSIFICATION

  • Stage I: one or more abscesses/inflammatory nodules without tunnels or scarring.
  • Stage II: recurrent abscesses with tunnels and scarring, with lesions separated by areas of relatively normal skin.
  • Stage III: diffuse or near-diffuse involvement with multiple interconnected tunnels and abscesses throughout an anatomical region.

Distribution

  • Axillae +++.
  • Inguinal folds +++.
  • Genital and perineal/perianal regions.
  • Inframammary folds.
  • Buttocks and intergluteal region.
  • Inner thighs.
  • Disease is often bilateral and recurrent at the same sites.

Dermoscopy

  • Dilated follicular openings and double-ended comedones may be visible.
  • Keratotic follicular structures.
  • Erythematous background in active inflammatory lesions.
  • Nonspecific vascular structures may occur.
  • Dermoscopy may provide additional information but is not required for diagnosis, which remains primarily clinical.

Diagnosis

  • Primarily a clinical diagnosis.
  • Based on three key features: characteristic morphology + typical intertriginous distribution + chronic/recurrent course.
  • No specific laboratory test is required in typical disease.
  • Bacterial cultures are not routinely required and are mainly indicated when secondary infection is suspected.
  • Cutaneous ultrasound may help determine the extent of subcutaneous tunnels, particularly when planning procedures.
  • Assess relevant comorbidities, including obesity, smoking, metabolic syndrome, depression/anxiety, and inflammatory bowel disease, when appropriate.

Differential diagnosis

  • Furuncle / furunculosis.
  • Bacterial skin abscess.
  • Inflamed or ruptured epidermoid cyst.
  • Pilonidal disease.
  • Perineal/cutaneous Crohn disease with fistulas.
  • Lymphogranuloma venereum.
  • Scrofuloderma.
  • Actinomycosis.
  • Other chronic inflammatory or infectious disorders causing abscesses and sinus tracts.

Treatment plan

  • Treatment depends on disease severity, inflammatory activity, tunnels/scarring, and impact on quality of life.
  • General measures include smoking cessation, weight management when appropriate, minimizing friction, and avoiding tight clothing.
  • Appropriate pain management is an important component of care.
  • Mild/localized disease: topical clindamycin 1% may be used, particularly for superficial inflammatory lesions.
  • Intralesional triamcinolone may be considered for selected acute, painful inflammatory nodules.
  • Mild-to-moderate inflammatory disease: oral tetracyclines, commonly doxycycline, may be used for their anti-inflammatory effect.
  • Selected patients may require systemic antibiotic combinations such as clindamycin + rifampin under medical supervision.
  • Moderate-to-severe disease: biologic therapy may be indicated; TNF or IL-17 inhibitors are among the available options depending on the patient, local guidelines, and treatment availability.
  • Hormonal therapies such as spironolactone or combined oral contraceptives may benefit selected female patients.
  • Incision and drainage alone provides temporary relief and has a high recurrence rate; it is generally not definitive HS treatment.
  • Recurrent nodules or tunnels: deroofing or targeted surgical excision.
  • Extensive scarred disease may require wide surgical excision.
  • Isotretinoin is not a standard first-line treatment for HS and has inconsistent efficacy; it may have a role in selected acne-associated phenotypes.
  • Psychological support and screening for depression/anxiety are important components of comprehensive management.

References

  1. DermNet — Hidradenitis suppurativa.
  2. American Academy of Dermatology (AAD) — Hidradenitis suppurativa.
  3. UpToDate — Hidradenitis suppurativa: Management.
  4. North American Clinical Management Guidelines for Hidradenitis Suppurativa.
  5. Bolognia JL, Schaffer JV, Cerroni L. Dermatology. Elsevier.