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Table · dataset · 2026

Supplementary file 1_Pediatric lymphomatoid papulosis: a broad clinicopathologic spectrum including rare variants in a single-center case series.docx

Listed in ZivaHub and HKU DataHub and figshare and Loughborough Research Repository and UP Research Data Repository — shown once because both records carry DOI 10.3389/fmed.2026.1948975.s001

Background<p>Lymphomatoid papulosis (LyP) is a rare CD30-positive cutaneous T-cell lymphoproliferative disorder, extremely uncommon in children and adolescents.

Description

Despite its indolent course, LyP may mimic malignant lymphomas clinically and histopathologically, making diagnosis challenging in pediatric patients.</p>Objectives<p>To characterize the clinical, histopathologic, immunophenotypic and molecular features of pediatric LyP and to describe treatment approaches and clinical outcomes.</p>Methods<p>We performed a retrospective observational study of pediatric patients with clinicopathologically confirmed LyP evaluated at our tertiary referral center between 2004 and 2025.

Demographic, clinical, histopathologic, immunophenotypic, molecular, treatment and follow-up data were collected.</p>Results<p>Nine patients were included (8 males, 1 female), with a median age at diagnosis of 11 years (range 2–18). Lesions predominantly involved the limbs (9/9, 100%), followed by the trunk (5/9, 56%) and hands (4/9, 44%). Ulceration or necrotic evolution occurred in 6/9 patients (67%).

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Type A was the most common histologic subtype (5/9, 56%), followed by single cases of types B, D, E and one overlap A–C case. CD30 expression was observed in all patients. T-cell receptor clonality was identified in 4/5 tested cases.

Management was mainly conservative, consisting of topical corticosteroids and phototherapy (nbUVB or PUVA). Methotrexate was used in one patient. At the last follow-up, all patients were free of active LyP lesions, and no associated hematologic malignancy was documented.</p>Conclusions<p>Pediatric LyP shows heterogeneous clinicopathologic features with overall favorable outcomes.

However, long-term follow-up remains warranted due to the lifelong risk of associated lymphoproliferative disorders.</p>

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Provenance · 5 source records, 45 field assertions
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ZivaHuboai:figshare.com:article/340213539 d agoJSON v1
HKU DataHuboai:figshare.com:article/340213539 d agoJSON v1
figshareoai:figshare.com:article/340213538 d agoJSON v1
Loughborough Research Repositoryoai:figshare.com:article/340213538 d agoJSON v1
UP Research Data Repositoryoai:figshare.com:article/340213538 d agoJSON v1
FieldAssertionExtractorEvidence
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