Review article
Hidradenitis suppurativa

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Pathogenesis

This disease was first documented in 1839 by Velpeau, who described a patient with an inflammatory process affecting the skin of the axillary, mammary, and perianal regions [3]. It was not until 1854, however, that it was suggested by Verneuil that the disease originated in the sweat glands [4]. In 1922, Schiefferdecker further classified sweat glands as apocrine or eccrine, and localized this disorder to the apocrine glands [5]. The histology was defined in 1939 by Brunsting, who suggested

Bacteriology

The bacterial flora involved in hidradenitis is inconsistent and unpredictable. Wounds in patients with positive cultures have grown bacteria such as Staphylococcus epidermidis, Escherichia coli, Klebsiella, Proteus, alpha Streptococcus, anaerobic bacteria, and diptheroids [8]. Thornton and Abcarian, however, found that half of their patients treated for perianal and perineal disease had negative cultures [10]. Highet and colleagues associated Streptococcus milleri infection with perineal

Etiology

The underlying reason for apocrine or follicular occlusion remains uncertain, though several predisposing factors have been suggested. Histologic studies have not demonstrated a difference in glandular structure to account for susceptibility to the disease [7]. Although the use of antiperspirants may prevent discharge of apocrine gland secretions and predispose the development of hidradenitis, Morgan and Leicester found no significant differences in shaving practices, deodorant usage, and

Incidence

The incidence of hidradenitis in the general population is unknown, mainly secondary to under reporting and misdiagnosis. However, it has been estimated that 1 in 300 adults is affected, usually presenting after puberty and before the age of forty [22]. Hidradenitis may be more common in females and blacks [25], [26], but perianal disease appears to be twice as common in males as in females [9], [13].

Clinical presentation

Any region of the body harboring apocrine glands may be involved, but the axillary and inguinal-perineal regions are most commonly affected [14]. Initially, patients will experience pain and present with indurated, deep subcutaneous nodules that organize as abscesses and may start spontaneously draining malodorous discharge. The wound usually does not heal completely, and recurrences are common. With each recurrence, the subcutaneous cavities tend to grow larger. The final result is an

Diagnosis

Differentiating hidradenitis from other cutaneous infections such as furuncles, carbuncles, lymphogranuloma venereum, erysipelas, epidermoid or dermoid cysts, and tuberculosis can be difficult [13], [27]. Perianal hidradenitis must be distinguished from other perianal pathology that can mimic its presentation. Cryptoglandular fistulae, for example, arise from the dentate line and involve the intersphincteric plane, whereas the tracts from hidradenitis do not involve the sphincter mechanism.

Treatment

Hidradenitis suppurativa presents as a spectrum of disease, ranging from mild, localized disease to extensive skin involvement in multiple affected areas. Treatment should be prioritized, with the most severe sites addressed first.

Summary

Hidradenitis suppurativa is a chronic, debilitating disease of apocrine gland-bearing skin. Its management must be individualized according to the site and extent of the disease. Initial conservative measures with antibiotics, local wound care, and limited incision and drainage can alleviate the acute symptoms, but more radical surgery will likely eventually be necessary in order to control and prevent recurrent disease. Options include unroofing and marsupialization, local excision, or more

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