No routine inspections
Suspecting HS is not a reason to inspect intimate body areas. What needs medical assessment is assessed in the practice, not by the family. Watch what is becoming difficult in daily life instead, and offer the appointment.
For parents and carers
What you might notice, how to raise it, how to help them get assessed — and where your child’s own authority over their body begins.
Recurring painful lumps or draining lesions in a child or teenager deserve medical attention — particularly when they come back or leave scars.
HS can begin during adolescence and is frequently recognised late in this age group. Your role is mainly to make access to care possible — while leaving your child increasing control over conversations about their own body.
The visible skin is rarely the clearest signal; what changes in daily life usually is. Every point below can be observed without looking at anything.
Suspecting HS is not a reason to inspect intimate body areas. Say what you have noticed instead, and offer to help get an appointment.
The left column keeps the conversation open; the right column usually ends it. The difference is almost always about who decides.
Helpful: “I’ve noticed this seems painful. Do you want help getting it checked?”
Better avoided: “Let me see.”
Why: An offer leaves the decision with the young person. A demand to see it takes away exactly the control they most need over an intimate part of their own body.
Helpful: “You don’t have to show me if you don’t want to. We can ask a doctor to look at it instead.”
Better avoided: “Have you been washing properly?”
Why: The hygiene question is medically wrong, and it lands squarely on the shame a young person has usually already brought with them.
Helpful: “This isn’t your fault, and you haven’t done anything wrong.”
Better avoided: “Why didn’t you tell me?”
Why: “Why didn’t you tell me?” lands as an accusation. The answer is almost always embarrassment, and that is a hard thing to say out loud.
Helpful: “Do you want to ask your own questions at the appointment, or shall I start?”
Better avoided: Answering on the young person’s behalf during the appointment without asking.
Why: A young person who gets to speak in the consulting room learns to do it alone later. Over time that matters more than an efficient appointment.
Helpful: “Tell me what actually helps right now — even small things.”
Better avoided: Comments about weight, diet or smoking as an explanation for the condition.
Why: Comments like these are heard as blame. What is medically relevant in an individual case belongs in the consultation — not at the kitchen table, and not on a website.
This section is communication support, not medical evidence. It reflects what young people with visible or intimate skin conditions describe as helpful or hurtful.
In practice, support usually means: booking the appointment, getting there, sorting out costs and paperwork, keeping dressings in the house, and persisting when a first assessment does not help.
If a practice tells you it is “just boils” and the lesions keep coming back, that is a reason to seek a dermatology second opinion — not a reason to stop.
Three places where well-meant support takes something away from the young person that should stay with them.
Suspecting HS is not a reason to inspect intimate body areas. What needs medical assessment is assessed in the practice, not by the family. Watch what is becoming difficult in daily life instead, and offer the appointment.
Ask before the appointment what the young person wants to say themselves — and whether part of the conversation should happen without you. If confidentiality matters to them, ask the practice together what applies: the rules depend on age, maturity, setting and country.
What has been studied in adults cannot simply be transferred to adolescents: the evidence base in younger patients is more limited, and age and developmental stage matter. Ask at the appointment which options are appropriate for your child — and involve them in that conversation as far as their development allows.
What the school needs to know is primarily your child’s decision. For many teenagers it is easier to hand over a short written note than to have the conversation themselves — there is a card here for that, built in the browser, and it does not have to name a diagnosis.
These pages deliberately name no medicines and give no age-based treatment recommendations. The evidence base in younger patients is more limited than in adults, and age, developmental stage and other conditions all matter.
Our treatment pages explain which categories of treatment exist at all. Which of them are appropriate for your child is something to settle at the appointment.
Nobody has to disclose a condition. “I don’t want to tell anyone yet” is a completely valid outcome of these pages.
Last editorially reviewed: · Next review:
That HS often begins during adolescence, usually after puberty starts, is described in reviews and in patient information from national health bodies. That it is not contagious and not caused by poor hygiene is well established.
That the condition is often recognised late in young people has been described repeatedly. The reported delays differ substantially between studies, because they use different data sources and definitions.
Quality-of-life research in younger patients consists mostly of small cross-sectional studies. They show that substantial burden can occur even when the skin looks relatively unaffected. They do not support any statement about how often that is the case overall.
A higher rate of new-onset depression among young people with HS has been reported in large retrospective cohorts. That says nothing about any individual — which is why these pages run no test and make no assessment.
Treatment recommendations for adults cannot be transferred to adolescents unexamined. The evidence base in younger patients is more limited, which is why these pages name no medicines and give no age-based treatment recommendations.