Am Fam Physician. 2005;72(8):1547-1552
A more recent article onhidradenitis suppurativa is available.
Patient information: See related handout on hidradenitis suppurativa, written by the author of this article.
Author disclosure: Nothing to disclose.
Hidradenitis suppurativa is a chronic, recurrent, debilitating disease that presents with painful, inflamed lesions in the apocrine-gland–bearing areas of the body, most commonly the axillary, inguinal, and anogenital areas. Etiology traditionally has been attributed to occlusion of the apocrine duct by a keratinous plug; however, defects of the follicular epithelium also have been noted. Contributing factors include friction from axillary adiposity, sweat, heat, stress, tight clothing, and genetic and hormonal components. Multiple treatment regimens are available, including antibiotics, retinoids, corticosteroids, incision and drainage, local wound care, local excision, radiation, and laser therapy. However, no single treatment has proved effective for all patients. Radical excision of the defective tissue is the most definitive treatment. The psychological impact on the patient can be great, encompassing social, personal, and occupational challenges. This impact should be addressed in all patients with significant disease.
Hidradenitis suppurativa (from the Greek hidros, sweat, and aden, glands), is also known as Verneuil’s disease or acne inversa, and occasionally is spelled hydradenitis. It is a common disorder, but its exact prevalence in the United States is unknown. A Danish study1 noted a prevalence of 4 percent in women. However, the diagnosis of hidradenitis suppurativa often is overlooked by physicians and therefore may be more common than is recognized. Hidradenitis suppurativa affects more women than men, with a female-to-male predominance as high as 4:1.2 This painful, disfiguring, and at times debilitating disease is marked by periods of inflammation with occasional secondary infection, and intermittent remissions that can last several years. The disease almost always occurs after puberty and before age 40, leading to the theory that there is a hormonal component to the pathogenesis. Flare-ups have been linked with menses3; shorter menstrual cycles and longer duration of menstrual flow are associated with the disease.1 There also seems to be a genetic component, and in one study3 of 110 patients, 38 percent reported a family history of this disease. This may reflect a familial form with autosomal dominant inheritance.4
The clinical presentation of hidradenitis suppurativa indicates the diagnosis. A thorough history and physical examination are recommended at the initial visit. Early symptoms may include discomfort, itching, erythema, burning, and hyperhidrosis. Hidradenitis manifests most commonly as tender, nodular lesions in the axillae (Figure 1), although other parts of the body also may be affected (Table 1 and Figure 2). If a single nodule appears, it may indicate one of several other skin lesions that manifest in a similar fashion, and distinguishing hidradenitis can be difficult. A differential diagnosis is given in Table 2.5–7 Nodules may have malodorous, superinfected drainage. Rarely, the patient has a fever or is septic, or both. In these instances, further work-up is based on laboratory findings. Complete blood count, blood cultures, and routine chemistries should be considered. Culture of the drainage is a reasonable option to help direct treatment.
|Axillae (most common)|
|Epidermoid or dermoid cyst|
|Tuberculosis (tuberculous inflammation of the skin)|
As the disease progresses, the diagnosis becomes more apparent, especially if the patient presents with frequent recurrences, scarring, fistulous tracks, and incomplete healing. The clinical course varies from occasional axillary lesions to diffuse abscess formations in multiple sites leading to chronic draining sinuses, as well as indurated, scarred skin and subcutaneous tissues. Some areas may coalesce to form tender, raised, violaceous dermis (Figure 3).
|Arthritis (certain forms)|
|Irritable bowel syndrome|
Potential complications of hidradenitis suppurativa include dermal contraction, local or systemic infection resulting from the spread of microorganisms, arthritis secondary to inflammatory injury, squamous cell carcinoma (in indolent sinus tracts), disseminated infection (rare), restricted limb mobility from scarring, lymphedema caused by lymphatic injury from inflammation and scarring, rectal or urethral fistulas, systemic amyloidosis, and anemia from chronic infection.11
There is no cure for hidradenitis suppurativa. However, several treatment options are available, including preventive, medical, surgical, and psychological strategies (Table 4). Because of the variety of ways in which the disease can manifest and progress, treatment should be based on the patient’s presentation and circumstances. Few high-quality randomized controlled trials or systemic reviews have addressed treatment of this condition.
|Mild||Early, solitary nodules with minimal pain; no abscesses||Avoidance of prolonged exposure to heat and humidity|
|Avoidance of shaving if irritation occurs|
|Avoidance of tight, synthetic clothing near affected area|
|Topical antiseptics and antibacterial soap|
|Warm compresses, warm baths, and hydrotherapy|
|NOT RECOMMENDED: Use of simple incision and drainage for lesions that are not fluctuant abscesses with purulent discharge|
|Moderate||Multiple, recurrent nodules with moderate pain; abscesses with purulent discharge||Antibiotics (topical, systemic, or both):|
|Cephalosporins (if patient has concurrent cellulitis)|
|Topical clindamycin (Cleocin)|
|Oral contraceptive agents, with high estrogen-to-progesterone ratio and low androgenicity of progesterone, in selected women|
|CONSIDER: Referral to a dermatologist (for patients who do not respond to initial therapy) or an early referral to an experienced general surgeon (discuss risks and benefits of surgery)|
|Severe||Diffuse abscess formation in multiple sites; chronic draining sinuses; indurated scarred skin and subcutaneous tissues||Referral to an experienced surgeon|
Although an abundance of anecdotal advice for the prevention of hidradenitis suppurativa exists, few methods have proved to be effective for all patients. In one study,3 24 percent of patients found nothing to help their condition, despite an average disease duration of almost 19 years.
For unknown reasons, women are more affected than men. Deodorants, shaving, and depilation have not been supported as a cause for this discrepancy in at least one study.12 However, these should be avoided if they cause irritation. Warm compresses, topical antiseptics, and antibacterial soap may help in patients with folliculitis. To help alleviate patient anxiety about the condition, physicians should emphasize that hidradenitis suppurativa is not caused by poor hygiene and is not contagious.
The progression of hidradenitis may be advanced by excessive underarm adiposity because this creates an ideal environment for bacterial growth and also produces friction. Therefore, one method of prevention may be weight loss. However, although losing weight improves symptoms, it does not provide a cure. Friction from clothing increases pain and discomfort, and patients should avoid wearing tight, synthetic clothing near the affected areas. Heat and humidity also have been associated with flare-ups, and prolonged exposure to hot, humid climates should be avoided if possible. Stress management methods may be useful because the disease can be aggravated during times of increased psychosocial stress.
Initial treatment of hidradenitis suppurativa can begin with conservative measures such as warm baths, hydrotherapy, and topical cleansing agents to reduce bacterial load.13 Nonsteroidal anti-inflammatory drugs may alleviate pain as well as inflammation. Antibiotics, although not proven to be effective, are the mainstay of medical treatment, especially for lesions suspected of being superinfected.
There is no evidence that chronic suppressive antibiotic therapy alters the natural history of hidradenitis. In a study3 of 110 patients with hidradenitis, the average duration of painful nodules was 6.9 days—about the duration of an average course of antibiotics. Therefore, the perceived response of hidradenitis suppurativa to antibiotics may be explained by the natural history of the condition itself, calling into question the routine use of antibiotics.3 One option is to culture the drainage from a large nodule and treat based on the results. Staphylococcus commonly is isolated; other pathogens include Escherichia coli and β-hemolytic streptococcus. Enteric flora may be found in cultures from perianal regions. Multiple organisms, including anaerobic bacteria, also may be found.8
Empiric antibiotic treatment may be given when conservative measures with several days’ observation have not improved symptoms. However, when superinfection is suspected it is best to treat based on culture results of drainage. Treatment can begin with topical or systemic antibiotics, or both. The only topical antibiotic that has been proven effective in a randomized controlled trial is clindamycin (Cleocin).1 Antistaphylococcal agents are best for axillary disease, and more broad-spectrum coverage is better for perineal disease. Dicloxacillin (Dynapen; 1 to 2 g daily), erythromycin (1 g daily), tetracycline (1 g daily), and minocycline (Minocin; 1 g daily) have been used. Cephalosporins may be helpful for concurrent active cellulitis. For severe, recurrent disease, anecdotal evidence suggests that two months or more of antibiotic therapy may be needed to prevent progression and worsening of concomitant infection.
Other medical treatment options address the possible hormonal etiology of hidradenitis; these options include oral contraceptive agents that contain a high estrogen-to-progesterone ratio and low androgenicity of progesterone.14 Two patients with severe, long-standing disease benefited from finasteride (Proscar) at a dosage of 5 mg daily.15 In Europe, the antiandrogen cyproterone acetate (Cyprostat) has been successful in some studies,16 but it currently is not approved for use in the United States.
Oral retinoids, which work by inhibiting sebaceous gland function and abnormal keratinization, also have been used. Pre-treatment with isotretinoin (Accutane) at a dosage of 0.5 to 1.0 mg per kg daily for a few months before surgery has been recommended to reduce the inflammatory components.17 No consensus on the dosing and duration of isotretinoin therapy has been reached by the few studies that have investigated it as a possible therapeutic option. Side effects of isotretinoin remain a major issue and include birth defects, hepatotoxicity, pseudotumor cerebri, and aggression.
Corticosteroids and immunosuppressants are other treatment possibilities. Topical tri-amcinolone (Aristocort) may be an option, but insufficient research has been conducted for it to be recommended routinely. Oral cyclosporine (Sandimmune) has shown some benefit, but chronic treatment can cause serious toxicity.18
For early, limited disease that presents with a fluctuant abscess, incision and drainage may be a good first option. However, this procedure provides only short-term relief and has little impact on the disease course. When hidradenitis sinus tracks are well established but relatively superficial, they can be unroofed or laid open.19 Because these tracks are lined by epithelium, the floor of the track can be preserved; this facilitates rapid healing and minimizes scarring.10
Early, rather than delayed, wide excisional therapy has been recommended by some experts as the treatment of choice because repeated failed treatments lead to the disease being more widespread and severe at presentation, making surgical options more difficult.17,20 Patients should be advised that surgery treats only the disease that is present at the site of the excision; recurrence at a new site is possible. In one study21 of 82 patients treated with wide excision, recurrence rates were zero percent for perianal disease, 3 percent for axillary disease, and 37 percent for inguinoperineal disease. Obesity, insufficient excision, significant skin maceration, and chronic skin infection may increase the incidence of recurrence.21 In another study,20 the overall complication rate was 17.8 percent; most complications were minor, such as suture dehiscence, postoperative bleeding, and hematoma. The rate of recurrence in this study was 2.5 percent and was related to the severity of the disorder.20
OTHER TREATMENT OPTIONS
Radiotherapy has been investigated as a potential treatment option. In a study22 of the effects of radiotherapy in 231 patients, 38 percent had complete relief, and 40 percent showed clear improvement of symptoms. However, the possibility of long-term side effects must be discussed thoroughly with the patient.
Cryotherapy also has been considered. In one small study,23 10 patients who did not respond to systemic antibiotics were given one cycle of cryotherapy; eight patients reported improvement. However, patients also experienced significant pain, prolonged healing time (average, 25 days), and post-treatment infection. A carbon dioxide laser used in conjunction with second-intention healing provided relief for a few patients.24
In addition to treating the physical illness, it is crucial that physicians acknowledge and treat the psychological burden associated with the disease. Because of the areas of the body that are affected, the malodorous discharge, the chronic discomfort, and the general unsightliness of the disease, hidradenitis suppurativa poses many challenges for patients in their personal life. Sexuality can be negatively affected. Unforgiving societal attitudes regarding inappropriate body odor (especially for those who choose not to wear deodorants), as well as years of inadequate treatment, may lead to frustration, depression, and isolation. For patients at increased risk for these outcomes, early surgical intervention should be strongly considered.17
Hidradenitis suppurativa remains a challenging disease for patients and physicians. Because there has been no significant research comparing treatment options, the choice of therapy should depend on the patient’s circumstances and preferences, the outcome of previous treatments, the experience of the physician, local expertise (e.g., a surgeon or dermatologist who specializes in treatment of the disease), and the chronicity and severity at presentation. Further research should be conducted not only on the etiology of this disease but also on the optimal treatment regimen.