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Hidradenitis suppurativa (HS) is a chronic inflammatory
disease resulting in suppurative, scarring lesions on apocrine gland-bearing
areas such as axillae, groin, and perigenital regions. HS is often a
disabling disease owing to chronically relapsing painful, discharging
lesions.
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ETIOLOGY |
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The cause is unknown. Predisposing factors include
obesity and genetic factors, and hormonal influences (androgen excess or
hyperresponsiveness).
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The pathomechanism is somewhat similar to acne.
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The primary event is occlusion of apocrine duct and
pilosebaceous follicle leading to obstruction of outflow of secretion.
Inflammatory changes in dilated apocrine duct and hair follicle takes place
with secondary bacterial infections. Rupture of gland/duct results in spread
of inflammation. Tissue destruction and suppuration leads to sinus formation
and fibrosis.
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CLINICAL FEATURES |
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Hidradenitis suppurativa begins after
puberty.
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Females are more commonly affected
than males.
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No racial predisposition.
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The typical sites of affection are:
axilla, groin, pubic region, perianal area, and buttocks. Bilateral
lesions are common.
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The initial lesions are painful and
tender, indurated, subcutaneous, reddish nodules.
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These lesions may subside or
suppurate and burst to discharge serous or seropurulent material. Deep
dermal involvement leads to indurated plaques.
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Draining sinus tracts
frequently develop.
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Subsequent fibrosis lead to scars
which are often band-like or hypertrophic and keloidal. Contracture of
the area may develop.
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Polyporous comedones
(blackheads with two or more openings that communicate inside skin) are
very characteristic.
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HS may rarely be a part of the so
called follicular occlusion triad (HS, acne conglobata,
perifolliculitis capitis) or tetrad ( the triad plus pilonidal
sinus).
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Hidradenitis suppurativa may have
considerable psychological impact with depression owing to chronic pain,
malodorous discharge and soiling of clothing, and involvement of
anogenital areas.
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DIFFERENTIAL DIAGNOSIS |
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DIAGNOSIS AND WORKUP |
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Typical clinical features of painful
nodules, discharging sinuses, thick scars and double comedones over areas
of predilections are fairly diagnostic.
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Culture and sensitivity of discharge
should be done. The organisms isolated may include Staph aureus,
streptococci, bacteroides sp., E. coli, proteus, and pseudomonads.
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Histopathologic features in early
phases show keratin occlusion of apocrine and hair follicle and
inflammatory changes. Late changes include destruction of appendages,
pseudoepitheliomatous hyperplasia, and fibrosis in association with
features of chronic inflammation.
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COURSE AND PROGNOSIS |
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- There is considerable variation in the severity and extent of the
disease.
- Some patients have recurrent painful nodules that subside without much
complication.
- Chronically relapsing and progressive course with many sinuses and
severe fibrosis in some patients can be quite disabling.
- Hidradenitis suppurativa tend to undergo spontaneous remission with
age (fourth decade)
- Chronic sequelae of hidradenitis suppurativa may include anemia,
amyloidosis, arthropathy ,and rarely squamous cell carcinoma.
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TREATMENT |
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Regular cleansing with antibacterial soaps.
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Correction of obesity.
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Antibacterials:
Long-term systemic antibacterials are treatment of choice in
chronic disease.. Tetracyline, doxycycline, minocyclne, and erythromycin
are preferred. Alternatives include co-trimoxazole, and metronidazole.
Topical antibacterials: clindamycin has been shown to give benefits.
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Isotretinoin : orally, may be helpful in early
disease in some patients.
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Intralesional triamcinolone helps resolution
of inflamed nodules in acute disease.
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Systemic steroid may be employed as a
concurrent therapy in severe inflammatory disease.
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Surgical treatment:
Incision and drainage of acute abscesses
Excision of areas of repeated recurrences in localized disease.
In widespread involvement, total excision of axilla or anogenital area
followed by grafting may be required.
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