[Of bugs and joints. Oligoarthritis caused by Tropheryma whipplei]

K Koligi1, D Mertz, D Benz

  • 1Felix Platter Spital, Rheumatologische Universitätspoliklinik, Burgfelderstrasse 101, 4012, Basel, Schweiz.

Der Internist
|November 4, 2010
PubMed

Insights

Whipple's disease, a rare bacterial infection, can manifest with joint pain for decades. Early detection via PCR in body fluids, beyond traditional biopsies, is crucial for timely treatment and improved outcomes.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Rheumatology

Background:

  • Whipple's disease is a rare, chronic infection caused by the bacterium Tropheryma whipplei.
  • Untreated, the disease has a high mortality rate, necessitating prompt antibiotic intervention.
  • Early symptoms often involve musculoskeletal issues like arthralgia and arthritis, preceding systemic manifestations.

Observation:

  • A 67-year-old male presented with a 30-year history of migratory oligoarthritis.
  • The causative agent, Tropheryma whipplei, was detected solely by polymerase chain reaction (PCR) in synovial fluid.
  • Standard diagnostic methods, including PAS-positive macrophages and duodenal PCR, were insufficient in this case.

Findings:

  • PCR analysis of affected tissues or body fluids is essential for diagnosing Whipple's disease.
  • Relying solely on duodenal biopsies may lead to missed or delayed diagnoses.
  • Synovial fluid PCR proved critical for identifying Tropheryma whipplei in this patient.

Implications:

  • Diagnostic strategies for Whipple's disease should incorporate PCR testing of various body fluids.
  • Treatment requires antibiotics with good cerebrospinal fluid penetration, such as ceftriaxone, followed by cotrimoxazole.
  • Prolonged antibiotic therapy over months to years is recommended, with pathogen clearance monitoring before discontinuation.

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