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Wide excision in a 67-year-old man with scrotal Paget's disease showed no recurrence and satisfactory outcomesA rare cancer hiding in plain sight for years

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Key Takeaway
Consider wide excision for scrotal Paget's disease, noting rare presentation and potential positive margins.

This study presents a case report and clinical analysis focusing on a 67-year-old man diagnosed with scrotal Paget's disease. The setting and specific publication type are noted as a systematic review context, though the core evidence derives from this single patient case. The primary intervention involved wide excision of the lesion, with regular follow-up conducted until no signs of recurrence were observed. Diagnostic strategies included histopathological evaluation, which demonstrated positivity for cytokeratin 7 (CK7), gross cystic disease fluid protein-15 (GCDFP-15), and podoplanin (D2-40). Frozen section analysis was also performed, revealing positive margins at the 1, 2, 6, and 11 o'clock positions.

The main results indicate satisfactory treatment outcomes for this patient. Specifically, no signs of recurrence were observed at the most recent follow-up point. The study also addresses prognosis management and diagnostic strategies as secondary outcomes. Safety and tolerability were not explicitly detailed with adverse event data in the provided evidence, and no serious adverse events or discontinuations were reported. The study design is limited by the inclusion of only one patient, which inherently restricts the statistical power and ability to draw broad conclusions.

Key limitations include the small sample size of one patient and the lack of reported funding or conflicts of interest. The practice relevance is that this case provides a valuable practical reference for the standardized diagnosis and treatment of this rare condition. However, clinicians should note that the positive margins found on frozen section analysis may influence surgical planning in similar cases. The evidence does not support causal claims due to the observational nature of the case report.

The lesion that kept coming back

A 67-year-old man walked into a hospital with a familiar problem. A skin patch on his scrotum had grown larger and started leaking fluid.

He had been here before — three times, in fact. Doctors had cut out similar lesions in the past.

Each time, they grew back.

The man had scrotal Paget's disease — a rare skin cancer that can start in sweat glands. Because it looks like eczema or a fungal rash, it often gets brushed off for years.

Most men have never heard of it. Even some doctors miss it on the first visit.

That delay matters. The longer this cancer sits, the deeper it can spread into nearby tissue and, in some cases, the lymph system.

The old way doctors saw this

For decades, stubborn groin or scrotal rashes got treated with creams. Steroids. Antifungals. A quick shave biopsy if things got worse.

If cancer was suspected, surgeons cut out the visible patch and hoped for the best.

But here's the twist — these lesions often spread underground. The cancer cells can reach well beyond the red patch you can see.

Hidden roots under the surface

Think of this cancer like a weed. The part above the soil is obvious. The roots below? They can stretch in every direction.

That's why simple removal often fails. Cells left behind regrow months or years later.

Modern care uses a tool called dermoscopy — a magnifying device that spots tell-tale patterns. In this patient, doctors saw a "red background with punctate vessels," a clue pointing to Paget's disease.

Doctors took a small sample first and confirmed the diagnosis. Then they planned a wide excision — cutting out the lesion plus a healthy margin around it.

During surgery, they tested the edges in real time with frozen section analysis. Cancer cells were still present at four spots on the border.

So they kept cutting until the edges came back clean.

The lab confirms the source

Lab tests showed the cancer cells came from sweat glands. Two proteins — CK7 and GCDFP-15 — pointed to that origin.

A third marker, D2-40, showed the cancer had the potential to spread through lymph channels.

That's a warning sign doctors take seriously.

A rash that heals with cream does not need a biopsy. A rash that keeps coming back does.

Why this report matters

This isn't a randomized trial. It's one patient's journey — what doctors call a case report.

But case reports like this one teach a generation of surgeons how to spot, cut, and follow up on a disease most will see only a handful of times in a career.

Scrotal Paget's disease sits in an awkward medical corner. It's too rare for large trials, but common enough that most urologists will encounter it.

Experts now favor intraoperative margin checking — testing tissue edges while the patient is still on the operating table. That way, no one leaves with cancer cells still hiding at the border.

Regular follow-up visits are also key. Recurrence can show up years later.

If you or a loved one has a skin patch in the groin, scrotum, or genital area that doesn't heal after weeks of treatment — ask for a biopsy.

Don't feel embarrassed. Dermatologists and urologists see these concerns every day.

Most patches turn out to be harmless. But the ones that aren't need early action.

This is a single case. Case reports raise hypotheses and teach technique — they don't prove what works best for every patient.

Larger studies are needed to pin down survival rates and the best follow-up schedule.

Researchers are exploring newer tools — like Mohs surgery, where skin is removed layer by layer with microscope checks between each slice. Targeted drugs for tough cases are also under study.

For now, the main lesson is simple. Rare doesn't mean impossible. If something on your skin keeps coming back, keep asking questions.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedApr 2026
View Original Abstract ↓
This study reports the case of a 67-year-old man with scrotal Paget’s disease. A systematic analysis of the clinical features, diagnostic and therapeutic strategies, and prognosis management of this rare disease was performed in conjunction with a literature review. The patient had a prolonged disease course with a history of three previous lesion excisions and presented this time due to lesion enlargement accompanied by mucous discharge. Dermoscopic examination revealed a “red background with punctate vessels,” and preoperative epidermal histopathology supported the diagnosis of Paget’s disease. The surgical approach involved wide excision of the lesion, aiming to remove the lesion as completely as possible while preserving the morphology and function of the surrounding tissues. Intraoperative frozen section analysis showed positive margins at the 1, 2, 6, and 11 o’clock positions. After further excision, immunohistochemical staining confirmed cytokeratin 7 (CK7) (+), gross cystic disease fluid protein-15 (GCDFP-15) (+), consistent with a sweat gland origin, and podoplanin (D2-40) (+), indicating a potential risk of lymphatic invasion. Finally, the patient was followed up regularly as planned, and at the most recent follow-up, no signs of recurrence were observed, and treatment outcomes were satisfactory, thereby allowing the discontinuation of further follow-up examinations. This case report provides a valuable practical reference for the standardized diagnosis and treatment of this rare condition.
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