Infectious Disease· Topic 7.17 Specific causative organisms· 7.17.56

Whipple disease

Whipple disease is a rare chronic infection with Tropheryma whipplei presenting with migratory arthralgia, diarrhea, steatorrhea, and weight loss, most often in middle-aged white men. Diagnosis is by small-bowel biopsy showing PAS-positive foamy macrophages, and treatment is intravenous ceftriaxone induction followed by long-term oral trimethoprim-sulfamethoxazole.

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What this article covers

  • Overview

    Whipple disease is a rare, chronic, multisystem infection caused by the gram-positive bacillus Tropheryma whipplei, an organism that establishes itself inside tissue macrophages and evades clearance.

  • Epidemiology

    Whipple disease is rare, with no established incidence or prevalence figure.

  • Risk factors

    Male sex: the disease occurs far more often in men than women.

  • Pathophysiology

    Tropheryma whipplei is a gram-positive, periodic acid-Schiff (PAS) positive actinomycete that infects tissue macrophages.

  • Clinical features

    Migratory large-joint arthralgia: the most common extraintestinal manifestation, affecting most patients; nonerosive and frequently precedes gastrointestinal symptoms by years.

  • Differential diagnosis

    Celiac disease: also causes diarrhea, weight loss, and malabsorption with iron-deficiency anemia, but tissue transglutaminase IgA antibody is positive and symptoms resolve on a gluten-free diet rather than requiring antibiotics.

  • Diagnosis

    Establishing test: the diagnosis is established by upper endoscopy with duodenal biopsy showing PAS-positive foamy macrophages in the lamina propria, since intestinal involvement is present in most…

  • Management

    First, confirm the diagnosis histologically or by PCR before starting a prolonged antibiotic course, since the standard regimen runs well over a year.

  • Complications

    Malabsorptive deficiencies: fat malabsorption produces vitamin D deficiency with hypocalcemia, vitamin K deficiency with an elevated prothrombin time and easy bruising, and vitamin B12 or folate deficiency with megaloblastic anemia.

  • Prognosis

    Whipple disease is fatal if untreated, progressing over years to malabsorptive wasting and, with CNS involvement, dementia and death.

  • Prevention

    Complete the full course of therapy: finishing the full 1 to 2 year maintenance course of TMP-SMX after ceftriaxone induction is the principal measure to prevent relapse.

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