# Late onset axial spondyloarthritis presenting with fever of unknown origin. A case-based review

**Authors:** Paraskevi V. Voulgari, Anastasia K. Zikou, Alexandros A. Drosos

PMC · DOI: 10.1007/s00296-026-06079-3 · 2026-02-20

## TL;DR

This paper presents a rare case of late-onset axial spondyloarthritis in an elderly woman who initially showed symptoms of fever of unknown origin.

## Contribution

The paper reports the first case of late-onset axial spondyloarthritis presenting with fever of unknown origin in an elderly patient.

## Key findings

- Late-onset axial spondyloarthritis can present with fever of unknown origin in elderly patients.
- The patient was successfully treated with adalimumab after extensive investigation ruled out other conditions.
- Physicians should consider rare SpA manifestations in elderly patients with unexplained fever and inflammation.

## Abstract

Spondyloarthritis (SpA) is a chronic inflammatory disease involving axial (ax-SpA), and peripheral joints (p-SpA). It mainly affects young individuals and symptoms begin before the age of 45 years. Late onset (LO) ax-SpA, presenting after the age of 50, is rare. It is usually underdiagnosed in favor of other disorders, which are very common in this population. A 70-year-old woman presented with fever of unknown origin (FUO), back pain, malaise, weakness and high acute phase reactants, without any other clinical or laboratory findings. After an intensive and extensive investigation, to exclude several diseases and disorders, our patient, despite being old and almost asymptomatic for SpA features was diagnosed as having LO-axSpA. The patient was treated successfully with adalimumab. We discuss the differential diagnosis of FUO in an elderly woman with constitutional symptoms and elevated inflammatory markers. This is the first case of LO-axSpA presenting with FUO, therefore, physicians must be aware of rare manifestations of ax-SpA in the elderly population. Rigorous and extensive investigation is required to reach the correct diagnosis.

## Linked entities

- **Diseases:** spondyloarthritis (MONDO:0005095)

## Full-text entities

- **Genes:** HLA-B (major histocompatibility complex, class I, B) [NCBI Gene 3106] {aka AS, B-4901, HLAB}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}
- **Diseases:** visual disturbances (MESH:D014786), pain (MESH:D010146), ReA (MESH:D016918), skin reactions (MESH:D012871), PMR (MESH:D011111), headache (MESH:D006261), inflammation (MESH:D007249), degenerative (MESH:D019636), vasculitis (MESH:D014657), morning stiffness (MESH:D048968), LO (MESH:D000067562), abdominal pain (MESH:D015746), hepatitis B and C (MESH:D006509), BME (MESH:D004487), malignancies (MESH:D009369), Spondylarthritis (MESH:D025241), weakness (MESH:D018908), hip (MESH:D025981), diarrhea (MESH:D003967), AS (MESH:D013167), acquired immunodeficiency virus (MESH:D000163), skin rashes (MESH:D005076), Febrile (MESH:D000071072), CMV (MESH:D003586), Andersson lesion (MESH:D009059), FUO (MESH:D005335), neck and back pain (MESH:D019547), claudication (MESH:D007383), PsA (MESH:D015535), psoriasis (MESH:D011565), Fever (MESH:D005334), hypertension (MESH:D006973), IBP (MESH:D001416), aortitis (MESH:D001025), arthritis (MESH:D001168), RA (MESH:D001172), joints (MESH:D007592), ERA (MESH:D001171), weight loss (MESH:D015431), arthralgia (MESH:D018771), cough (MESH:D003371), sacroiliitis (MESH:D058566), mucosal ulcers (MESH:D014456), ARD (MESH:D012216), infections (MESH:D007239), P (MESH:D002972), axSpA (MESH:D000089183), infectious spondylitis (MESH:D013166), Anderson and Romanus lesions (MESH:C535460), Raynaud's phenomenon (MESH:D011928), myalgia (MESH:D063806), musculoskeletal problems (MESH:D009140), infective endocarditis (MESH:D004696), IBD (MESH:D015212), axial disease (MESH:C537791), ACD (MESH:D002908)
- **Chemicals:** adalimumab (MESH:D000068879), infliximab (MESH:D000069285), ferrum (-), naproxen (MESH:D009288), prednisone (MESH:D011241), amlodipine (MESH:D017311)
- **Species:** Human immunodeficiency virus 1 (no rank) [taxon 11676], Homo sapiens (human, species) [taxon 9606], human gammaherpesvirus 4 (Epstein Barr virus, no rank) [taxon 10376]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923395/full.md

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Source: https://tomesphere.com/paper/PMC12923395