An 18-year-old man had inflammatory acne lesions on the face, back and upper arm two years ago. He was treated with oral cefdinir, topical antimicrobials and benzoyl peroxide (BPO) two years ago. However, the lesions did not respond to these treatments.

Numerous multiple painful nodulocystic lesions, pustules, and necrotic hemorrhagic ulcerative lesions with crusts developed the face, back, chest and upper arm two weeks ago. Systemic symptoms such as fever, general fatigue and arthralgia were not observed. Movement restriction caused by pain was observed in the shoulder joint. He was diagnosed as acne fulminans (AF). Laboratory findings revealed an elevated white blood cell (WBC) count (20,300/μl) (normal level: 4000 - 9000/μl) with a neutrophilia and C-reactive protein (CRP) (3.91 mg/dl) (normal level: below 0.30 mg/dl). Notably, Staphylococcus epidermidis was detected in the bacterial culture from the lesion.

Initially, the patient was treated with oral faropenem 600 mg/d and Saireito 8.1 g/d (Japanese Herb) for two weeks. Subsequently, he was treated with oral minocycline 100 mg/d. The lesions did not respond to these treatments and rather developed into a hemorrhagic ulcer (Figure 1(a)). Consequently, he was treated with additional oral prednisolone (20 mg/d) for two weeks. The lesions showed remarkable improvement promptly. The hemorrhagic ulcerations were re-epithelialized, resulting in postinflammatory hyperpigmentation (Figure 1(b)). In addition, the pain subsided quickly, and movement restriction in the shoulder joint was improved.

The informed consent was obtained from the patient to reproduce the clinical findings.

AF is usually defined as a sudden onset severe ulcerative acne with toxic effects such as fever, weight loss and arthralgia. It fails to respond to antimicrobial therapy and shows favorable responses to debridement in combination with steroid therapy [1] [2]. AF is exclusively observed in adolescents of age ranging from 13 - 16 years [1] [2]. Notably, this condition is more frequently observed in males than in females [1] [2], and its clinical manifestation includes hemorrhagic ulcerations with pain [1] [2]. AF without systemic symptoms and abnormal laboratory findings were reported as AF “sine fulminans” [3]. In our case, a sudden onset was observed with painful hemorrhagic necrotic ulcers with crusts. Additionally, increased WBC count with neutrophilia and elevated CRP were observed. In spite of unresponsiveness by antimicrobial therapy, the lesions responded to corticosteroid therapy. In view of the above-mentioned findings, our patient was diagnosed with AF.

The etiology of AF is unclear. The immunological response to Cutibacterium acnes (C. acnes), neutrophil function, hypersensitive responses to either sebum or bacterial antigens, and genetic factors might be responsible [4].

As differential diagnosis, acne conglobata (AC) is considered. AC is usually observed in adults [4]. The clinical manifestations of AC mainly include nodules, cysts, and polyporus comedones [4].

Concerning therapy for AF, a combination therapy with corticosteroids and isotretinoin is highly recommended [1]. However, the use of isotretinoin is not allowed in Japan. Isotretinoin may precipitate AF as it promotes fragility of the sebaceous duct, resulting in significant contact with C. acnes [1].

The long-term prognosis of AF after the treatment is good without recurrence.

A case of acne fulminans without systemic symptom successfully treated with oral corticosteroids has been reported.

The author declares no conflicts of interest regarding the publication of this paper.

Kurokawa, I. (2020) Effective Treatment of Acne Fulminans with Oral Corticosteroids. Journal of Cosmetics, Dermatological Sciences and Applications, 10, 107-109. https://doi.org/10.4236/jcdsa.2020.103012