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Clinical Examination Protocol to Detect Atypical and Classical Scrapie in Sheep
Published on: January 19, 2014
[Pyogenic sacroiliitis: Lessons learned from an atypical case series]
Joana Arcângelo1, Susana Norte Ramos2, Pedro Alves3
1Unidad de Ortopedia, Hospital Curry Cabral, Centro Hospitalar de Lisboa Central, EPE, Lisboa, Portugal.
Insights
Pyogenic sacroiliitis (PSI) in children is hard to diagnose, with blood cultures often negative. Early suspicion and advanced diagnostics like PCR are crucial for identifying atypical agents and ensuring effective treatment.
Area of Science:
- Pediatric Infectious Diseases
- Musculoskeletal Infections
- Microbiology
Background:
- Pyogenic sacroiliitis (PSI) is a rare pediatric joint infection (1-2% of cases).
- Diagnosis is challenging due to nonspecific signs and symptoms.
- Identifying causative microorganisms is difficult due to negative blood cultures and risks of joint aspiration.
Purpose of the Study:
- To review cases of pediatric pyogenic sacroiliitis.
- To evaluate diagnostic challenges and causative agents.
- To assess treatment outcomes and identify optimal diagnostic strategies.
Main Methods:
- Retrospective review of pediatric patients (<18 years) with PSI.
- Analysis of medical records from 2008-2016.
- Inclusion of diagnostic methods used (blood cultures, joint aspiration, specific screening tests).
Main Results:
- Six pediatric PSI cases were identified.
- Blood cultures were consistently negative.
- Causative agents included Aggregatibacter aphrophilus, Kingella kingae, Brucella melitensis, and Bartonella henselae, requiring joint aspiration or specific screening.
- All patients achieved favorable outcomes with targeted antimicrobial therapy.
Conclusions:
- Blood cultures have low effectiveness for diagnosing pediatric PSI.
- A high index of suspicion for atypical agents is necessary.
- Early use of advanced diagnostics (imaging, serology, PCR) and appropriate antimicrobial therapy are essential for successful management.
Introduction:
Pyogenic sacroiliitis (PSI) is a rare condition that amounts to 1% to 2% of all joint infections in the paediatric age group. Its diagnosis is often difficult and delayed due to its nonspecific signs, symptoms and physical findings. Also, the identification of the causative microorganism is frequently challenging due to a high proportion of negative blood cultures and the risks involved in joint aspiration in this site.
Patients And Methods:
We performed a retrospective review of the health records of all patients aged less than 18 years admitted to a tertiary children's hospital due to PSI between 2008 and 2016.
Results:
We identified 6 cases of paediatric PSI. The blood cultures were negative, and the identification of the causative agent required joint fluid aspiration in one patient with infection by Aggregatibacter aphrophilus, and specific screening tests for less frequent agents in the other patients: Kingella kingae (n=2), Brucella melitensis (n=1) and Bartonella henselae (n=1). The patients were treated with specific antimicrobial regimens, and all had favourable clinical outcomes and were free from sequelae during the follow-up.
Conclusions:
Despite the small sample size, our study evinced the low effectiveness of blood cultures for diagnosis of paediatric PSI. It also highlights the need for a high level of suspicion for atypical agents and the early use of adequate diagnostic methods, including imaging and serological testing or polymerase chain-reaction (PCR) analysis of blood samples, as well as prescription of effective antimicrobial therapy.
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