# Case Report: Siblings with neonatal lupus erythematosus

**Authors:** Pengyue Tang, Huan Zhang, Ping Li

PMC · DOI: 10.3389/fped.2025.1518881 · 2025-03-03

## TL;DR

This case report describes two siblings with neonatal lupus erythematosus, highlighting the importance of early diagnosis and monitoring in high-risk pregnancies.

## Contribution

The report emphasizes variable NLE phenotypes within families and the impact of inconsistent maternal treatment on disease occurrence.

## Key findings

- Two siblings presented with distinct NLE manifestations despite similar serologic findings.
- The mother's suboptimal treatment adherence may have contributed to NLE in the second child.
- Regular monitoring is essential for early detection and management of NLE in high-risk pregnancies.

## Abstract

Neonatal lupus erythematosus (NLE) is a rare autoimmune disorder characterized by cutaneous and/or cardiac manifestations resulting from the transplacental passage of maternal antibodies, including anti-SSA/Ro, anti-SSB/La, and occasionally anti-U1RNP. This report describes two siblings with distinct NLE presentations, emphasizing the importance of early diagnosis and management, particularly in light of the rising rates of multiple births. A 15-day-old girl (Case 1) presented with classic annular skin lesions and strongly positive SSA and SSB antibodies. Six years later, her brother (Case 2) developed atypical red papules with similar serologic findings. Their mother, diagnosed with Sjögren's syndrome after the first child's (Case 1) presentation, demonstrated suboptimal treatment adherence, which may have contributed to the occurrence of NLE in her second child (Case 2). Neither sibling exhibited systemic involvement, including cardiac manifestations; however, regular monitoring remains essential. These cases highlight the variable NLE phenotype, even within families. In pregnancies with SSA/SSB antibody positivity, close monitoring of antibody titers, electrocardiograms (ECGs), and echocardiograms is paramount for early NLE detection and optimal management, especially given inconsistent maternal treatment. These cases underscore the need for heightened vigilance and proactive strategies in high-risk pregnancies.

## Linked entities

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

## Full-text entities

- **Genes:** TRIM21 (tripartite motif containing 21) [NCBI Gene 6737] {aka RNF81, RO52, Ro/SSA, SSA, SSA1, TRIM21/Ro52}, SSB (small RNA binding exonuclease protection factor La) [NCBI Gene 6741] {aka LARP3, La, La/SSB, SSB/La}, SNRNP70 (small nuclear ribonucleoprotein U1 subunit 70) [NCBI Gene 6625] {aka RNPU1Z, RPU1, SNRP70, Snp1, U1-70K, U170K}
- **Diseases:** annular (MESH:D016460), skin lesions (MESH:D012871), Sjogren's syndrome (MESH:D012859), NLE (MESH:C536397), autoimmune disorder (MESH:D001327)

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11911384/full.md

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Source: https://tomesphere.com/paper/PMC11911384