Short answer · Medically reviewed summary · Last updated: 2026-04-07
TL;DR: Hidradenitis suppurativa is diagnosed primarily through a clinical examination by a dermatologist who evaluates the location, appearance, and recurrence of painful skin lesions. There is currently no single blood test or genetic marker to identify the condition, making a thorough physical assessment and medical history review the gold standard for diagnosis. How is a diagnosis of Hidradenitis Suppurativa reached? Because there is no definitive laboratory test for hidradenitis suppurativa, the diagnosis is based on clinical presentation.
6 people with Hidradenitis Suppurativa have shared their first-person experience on this question at DiseaseMaps.
TL;DR: Hidradenitis suppurativa is diagnosed primarily through a clinical examination by a dermatologist who evaluates the location, appearance, and recurrence of painful skin lesions. There is currently no single blood test or genetic marker to identify the condition, making a thorough physical assessment and medical history review the gold standard for diagnosis.
Because there is no definitive laboratory test for hidradenitis suppurativa, the diagnosis is based on clinical presentation. A dermatologist will typically look for three specific criteria: the presence of typical lesions (such as nodules, abscesses, or sinus tracts), a characteristic distribution in areas like the armpits or groin, and a history of recurrence. Many patients experience a long "diagnostic odyssey," often waiting several years to receive an accurate diagnosis, as the condition is frequently misidentified as simple boils or poor hygiene.
While the diagnosis is clinical, physicians may use specific investigations to rule out other infections or complications. Hidradenitis suppurativa diagnostics may include:
Hidradenitis suppurativa is frequently confused with other conditions, which contributes to the delay in diagnosis. Doctors must distinguish it from common skin issues, including furunculosis (multiple boils), pilonidal cysts, Crohn’s disease (which can present with similar perianal lesions), and lymphadenitis. Because hidradenitis suppurativa affects the immune and endocrine systems, it is vital to differentiate it from other folliculitis-related disorders to ensure the correct treatment plan—such as biologics or specialized surgical interventions—is initiated.
We understand that the journey to diagnosis can be exhausting and isolating. With 729 members of the DiseaseMaps community currently navigating life with hidradenitis suppurativa, we know that many patients are told their symptoms are related to weight or hygiene, which is clinically inaccurate. Seeking a board-certified dermatologist who specializes in inflammatory skin conditions is crucial. A specialist will recognize the systemic nature of hidradenitis suppurativa and can prevent the progression toward severe scarring or systemic infections by starting appropriate anti-inflammatory or immunosuppressive therapy early.
Medical disclaimer: This content is for informational purposes only and does not constitute medical advice, diagnosis, or treatment; always seek the advice of your physician or other qualified health provider with any questions regarding a medical condition.