Plate 07
Hidradenitis Suppurativa
Also called: Acne inversa · Verneuil disease
Follicular & facialGeneral 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
- DermNet — Hidradenitis suppurativa.
- American Academy of Dermatology (AAD) — Hidradenitis suppurativa.
- UpToDate — Hidradenitis suppurativa: Management.
- North American Clinical Management Guidelines for Hidradenitis Suppurativa.
- Bolognia JL, Schaffer JV, Cerroni L. Dermatology. Elsevier.