# Twin Presentation of Cutaneous Neonatal Lupus Associated With Maternal Anti-U1RNP Antibodies: A Case Report

**Authors:** Sofia Guedes, Patrícia Veríssimo, Ana T Maria, Mónica Marçal

PMC · DOI: 10.7759/cureus.101451 · Cureus · 2026-01-13

## TL;DR

This case report describes twin girls with a rare skin condition caused by maternal antibodies, highlighting new insights into neonatal lupus and its connection to maternal autoimmunity.

## Contribution

The first reported case of anti-U1RNP neonatal lupus in twins with catheter-aligned skin lesions and maternal autoimmunity.

## Key findings

- Twin girls developed cutaneous neonatal lupus associated with maternal anti-U1RNP antibodies.
- Lesions aligned with catheters suggest trauma-induced Koebnerization as a trigger.
- Maternal autoimmunity was identified through neonatal findings.

## Abstract

Neonatal lupus erythematosus (NLE) is a rare autoimmune condition caused by the transplacental transfer of maternal IgG autoantibodies, most commonly anti-Sjögren's-syndrome-related antigen A (anti-Ro/SSA) and anti-Sjögren’s-syndrome-related antigen B (anti-La/SSB). NLE associated solely with anti-U1RNP antibodies is uncommon and typically limited to cutaneous manifestations, with extremely few cases reported in twins. We describe bi-chorionic bi-amniotic preterm twin girls who developed atypical erythematous lesions along the trajectory of epicutaneo-cava catheters during the second week of life. Autoimmune screening revealed strongly positive anti-U1RNP antibodies in both infants; cardiac evaluation was normal. Autoantibodies became negative by eight months. Both twins showed normal development and no further manifestations at 15 months. Maternal evaluation uncovered previously unrecognized antinuclear antibody (ANA) and anti-ribonucleoprotein antibody(anti-RNP) positivity. This appears to be the first reported case of anti-U1RNP NLE presenting with catheter-aligned inflammatory lesions in twins. The case highlights the role of trauma-induced Koebnerization as a potential trigger and underscores the importance of considering autoimmune etiologies in synchronous neonatal skin lesions, as well as the value of neonatal findings in identifying occult maternal autoimmunity.

## Linked entities

- **Diseases:** neonatal lupus erythematosus (MONDO:0018360), lupus (MONDO:0004670)

## Full-text entities

- **Genes:** RNPC3 (RNA binding region (RNP1, RRM) containing 3) [NCBI Gene 55599] {aka CPHD7, IGHD5, RBM40, RNP, SNRNP65}, SNRNP70 (small nuclear ribonucleoprotein U1 subunit 70) [NCBI Gene 6625] {aka RNPU1Z, RPU1, SNRP70, Snp1, U1-70K, U170K}, SSB (small RNA binding exonuclease protection factor La) [NCBI Gene 6741] {aka LARP3, La, La/SSB, SSB/La}
- **Diseases:** erythematous lesions (MESH:D009059), autoimmune condition (MESH:D001327), trauma (MESH:D014947), inflammatory (MESH:D007249), skin lesions (MESH:D012871), Cutaneous Neonatal Lupus (MESH:C536397)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12900119/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12900119/full.md

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Source: https://tomesphere.com/paper/PMC12900119