
- Dermatology Times, Advancing Hidradenitis Suppurativa Care: Early Diagnosis, Biologic Therapies, and Multidisciplinary Approaches, March 2025 (Vol. 46. Supp. 01)
- Volume 46
- Issue 01
Advancing Hidradenitis Suppurativa Care - Early Diagnosis, Biologic Therapies, and Multidisciplinary Approaches: Part 1
Key Takeaways
- Hidradenitis suppurativa significantly impacts patients' lives, with early onset disrupting education, careers, and relationships, and causing severe physical and mental health issues.
- Delays in HS diagnosis, often spanning 7 to 10 years, contribute to irreversible tissue damage, highlighting the need for early detection and intervention.
In part 1 of this Frontline Forum supplement, experts discuss the burden of HS, reducing diagnostic delays, and more.
In the recent Dermatology Times Frontline Forum custom video series “
Addressing the Burden of HS
Elias, a board-certified dermatologist at Elias Dermatology in Pembroke Pines, Florida, and Lev-Tov, a board-certified dermatologist and associate professor of clinical dermatology and cutaneous surgery at the University of Miami Miller School of Medicine in Florida, kicked off the panel discussion by reviewing the challenging burden for patients with HS. Lev-Tov described HS as one of the “cruelest” skin diseases due to its early onset and severe impact on patients’ lives. Affecting between 0.1% and 1% of the global population, HS typically manifests during young adulthood, disrupting key milestones such as education, career development, and relationships. The disease’s physical symptoms—painful abscesses, scarring, and sinus tract formation—are compounded by significant mental health comorbidities, including depression, anxiety, and elevated suicide rates.
From a health care perspective, HS demands attention due to its prevalence and complexity. “One of the contributing factors here is the delay to diagnosis,” Lev-Tov said. Patients often face delays of 7 to 10 years before receiving a diagnosis, during which time irreversible tissue damage may occur. Lev-Tov emphasized that early diagnosis within the “window of opportunity” can significantly improve outcomes given the advancements in medical therapies.
Raising Awareness to Reduce Diagnostic Delays
One of the core challenges in HS management and treatment is increasing awareness among health care providers and the broader community, according to the panelists. Misdiagnosis is often common, as nondermatology clinicians may unknowingly mistake HS for abscesses. Elias advocated for collaborative education efforts, such as grand rounds in local surgery departments and lectures at medical societies. These initiatives aim to equip nondermatology clinicians with the knowledge to identify and refer HS cases accurately.
Integrating HS into medical school curricula was proposed as a strategy to familiarize future clinicians with this high-burden disease. Lev-Tov highlighted the importance of interdisciplinary collaboration, noting that HS touches multiple specialties, including endocrinology, gastroenterology, and pain management. Supporting organizations such as the HS Foundation, which advocates for patients and provides educational resources, is crucial in amplifying these efforts.
Discussion continued in part 2.
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