Background: Hidradenitis suppurativa (HS) is a chronic, recurrent inflammatory disorder of the hair follicle that predominantly affects areas rich in apocrine sweat glands, such as the axillae and groin. Clinically, it is characterized by painful nodules, abscess formation, sinus tract development, and scarring. Diagnosis is primarily based on clinical findings; however, due to limited awareness of the disease, it is often diagnosed at a late stage. Misdiagnosis and inappropriate management are common, leading to chronic disease progression. Consequently, HS significantly impairs quality of life through reduced work capacity, psychological distress, and social isolation. Disease severity is commonly assessed using the Hurley staging system and the Sartorius scoring system. We present a rare case of hidradenitis suppurativa encountered in dermatological practice. Case presentation A 35-year-old male patient (initials L.B.) presented with recurrent, painful lesions in both axillary regions associated with purulent discharge. The condition had persisted over a prolonged period with repeated exacerbations. The patient had attempted self-treatment at home without improvement and was subsequently admitted to the Department of Dermatology at the National Center for Dermatology with a diagnosis of DS: L73.2 (hidradenitis suppurativa). The patient was treated with systemic antibiotics (doxycycline and cefazolin), retinoids, supportive therapy, and topical treatment. In addition, intralesional triamcinolone injections were administered into active nodules, which proved effective in rapidly reducing inflammation, pain, and purulent discharge.