# Hemophagocytic Lymphohistiocytosis in a Patient With Hodgkin’s Lymphoma Mimicking Sinusoidal Obstructive Syndrome: A Diagnostic Challenge

**Authors:** Monica Soliman, Deepa Lazarous

PMC · DOI: 10.7759/cureus.85397 · Cureus · 2025-06-05

## TL;DR

A young man with Hodgkin’s lymphoma developed a rare inflammatory condition mistaken for another liver syndrome, highlighting the importance of accurate diagnosis for timely treatment.

## Contribution

Highlights the diagnostic challenge of HLH in lymphoma patients and emphasizes the need for early recognition to avoid treatment delays.

## Key findings

- HLH was initially misdiagnosed as sinusoidal obstructive syndrome in a Hodgkin’s lymphoma patient.
- Elevated serum ferritin and sCD25, along with bone marrow hemophagocytosis, confirmed HLH diagnosis.
- High-dose corticosteroids led to rapid clinical improvement in the patient.

## Abstract

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening hyperinflammatory syndrome triggered by malignancy, infection, or autoimmune disease. We present a case of a 19-year-old male with Hodgkin’s lymphoma who developed high-grade fevers, hepatomegaly, and severe liver injury shortly after receiving chemotherapy. He was initially diagnosed with sinusoidal obstructive syndrome (SOS) and treated with defibrotide. Despite therapy, his condition deteriorated, prompting transfer to our institution for evaluation of acute liver failure and suspected drug-induced liver injury (DILI). Further diagnostic evaluation revealed markedly elevated serum ferritin and soluble interleukin-2 receptor (sCD25), and bone marrow biopsy demonstrated prominent hemophagocytosis. These findings confirmed the diagnosis of HLH, likely secondary to underlying Hodgkin’s lymphoma and possible Epstein-Barr virus (EBV) reactivation. The patient was initiated on high-dose corticosteroids with rapid clinical and biochemical improvement. This case underscores the diagnostic complexity of HLH, particularly in lymphoma patients undergoing chemotherapy, where overlapping syndromes can delay accurate diagnosis, and highlights the critical importance of early recognition to initiate timely, life-saving immunosuppressive therapy.

## Linked entities

- **Proteins:** ferritin (soma ferritin-like)
- **Diseases:** Hemophagocytic Lymphohistiocytosis (MONDO:0015540), Hodgkin’s Lymphoma (MONDO:0004952), drug-induced liver injury (MONDO:0005359)

## Full-text entities

- **Diseases:** infection (MESH:D007239), fevers (MESH:D005334), lymphoma (MESH:D008223), HLH (MESH:D051359), autoimmune disease (MESH:D001327), SOS (MESH:D006504), malignancy (MESH:D009369), DILI (MESH:D056486), liver injury (MESH:D017093), acute liver failure (MESH:D017114), hepatomegaly (MESH:D006529), hyperinflammatory syndrome (MESH:D013577), Hodgkin's Lymphoma (MESH:D006689)
- **Chemicals:** defibrotide (MESH:C036901)
- **Species:** human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

9 references — full list in the complete paper: https://tomesphere.com/paper/PMC12228357/full.md

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Source: https://tomesphere.com/paper/PMC12228357