# Life-Threatening Macrophage Activation Syndrome in Pregnancy: First Manifestation of SLE Induced by Parvovirus B19

**Authors:** Aleksandra Plavsic, Rada Miskovic, Dragana Jovanovic, Uros Karic, Zikica Jovicic, Sara Radovic, Ana Drazic, Aleksandra Dasic, Snezana Arandjelovic

PMC · DOI: 10.3390/ijms26115406 · 2025-06-04

## TL;DR

A pregnant woman developed a rare and severe immune condition linked to lupus and a virus, requiring termination of the pregnancy and long-term treatment.

## Contribution

This case is the first reported instance of SLE-induced MAS during pregnancy triggered by Parvovirus B19.

## Key findings

- A 30-year-old pregnant woman developed MAS and SLE, likely triggered by Parvovirus B19 infection.
- The patient required termination of pregnancy and long-term immunosuppressive therapy for SLE.
- Parvovirus B19 IgM antibodies confirmed the infection's role as a trigger for MAS and SLE onset.

## Abstract

Macrophage activation syndrome (MAS) is a complex, life-threatening, hyperinflammatory condition occurring as a form of hemophagocytic lymphohistiocytosis (HLH), commonly associated with several autoimmune and autoinflammatory diseases, and certain infections such as Parvovirus B19 (P19V). The onset of systemic lupus erythematosus (SLE) presenting as MAS during pregnancy is uncommon, posing significant diagnostic and therapeutic challenges. We present a case of a 30-year-old woman at the 12th gestational week with fever, arthralgia, rash, cervical lymphadenopathy, cytopenia, and elevated liver enzyme. Bone marrow biopsy revealing hemophagocytosis, elevated ferritin and triglycerides, high interleukin-2, fever and cytopenia, confirmed the diagnosis of HLH. Further evaluation revealed the diagnosis of SLE. Treatment was initiated with intravenous immunoglobulin and corticosteroids. Given the deterioration in the patient’s clinical condition, a decision was made to terminate the pregnancy. She continued in the following months to receive SLE treatment with corticosteroids, cyclophosphamide, hydroxychloroquine, and later with mycophenolate mofetil due to the development of Class IV of lupus nephritis. P19V IgM antibodies were initially positive, later seroconverted to IgG, indicating that infection may have acted as a trigger for the onset of SLE and MAS development during pregnancy. The overlapping clinical features of P19V infection, SLE, and MAS pose significant diagnostic and therapeutic challenges. Early recognition and comprehensive diagnostic evaluation are crucial for the management of these conditions, especially during pregnancy, where both maternal outcomes are at risk.

## Linked entities

- **Diseases:** macrophage activation syndrome (MONDO:0015545), systemic lupus erythematosus (MONDO:0007915), lupus nephritis (MONDO:0005556)

## Full-text entities

- **Genes:** IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}
- **Diseases:** lupus nephritis (MESH:D008181), arthralgia (MESH:D018771), MAS (MESH:D055501), autoimmune and autoinflammatory diseases (MESH:D056660), SLE (MESH:D008180), P19V infection (MESH:D007239), fever (MESH:D005334), rash (MESH:D005076), cytopenia (MESH:D006402), HLH (MESH:D051359), lymphadenopathy (MESH:D008206)
- **Chemicals:** cyclophosphamide (MESH:D003520), triglycerides (MESH:D014280), mycophenolate mofetil (MESH:D009173), hydroxychloroquine (MESH:D006886)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human parvovirus B19 (no rank) [taxon 10798]
- **Mutations:** P19V

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12155505/full.md

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Source: https://tomesphere.com/paper/PMC12155505