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For further information, see CMDT Part 15-27: Malabsorption
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Essentials of Diagnosis
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Multisystem disease
Fever, lymphadenopathy, arthralgias
Weight loss, malabsorption, chronic diarrhea
Duodenal biopsy with periodic acid-Schiff (PAS)–positive macrophages with characteristic bacillus
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General Considerations
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Clinical manifestations are protean
However, the most common are arthralgias, diarrhea, abdominal pain, and weight loss
Arthralgias or a migratory, nondeforming arthritis in 80%
Gastrointestinal symptoms in 75% include
Weight loss in almost all patients
Protein-losing enteropathy with hypoalbuminemia and edema
Intermittent low-grade fever in > 50%
Generalized lymphadenopathy
Myocardial involvement: heart failure or valvular regurgitation
CNS involvement
Dementia
Lethargy
Coma
Seizures
Myoclonus
Hypothalamic dysfunction
Cranial nerve findings: ophthalmoplegia or nystagmus
Physical examination
Low-grade fever
Hypotension (late)
Evidence of malabsorption
Lymphadenopathy (in 50%)
Heart murmurs
Peripheral joint inflammation, swelling
Neurologic findings
Hyperpigmentation on sun-exposed areas (in up to 40%)
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Differential Diagnosis
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Malabsorption due to other cause, eg, celiac disease
Inflammatory bowel disease
Sarcoidosis
Reactive arthritis
Systemic vasculitis
Infective endocarditis
Intestinal lymphoma
Familial Mediterranean fever
Behçet syndrome
Intestinal Mycobacterium avium-intracellulare (in AIDS)
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Diagnostic Procedures
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Ceftriaxone, 1 g intravenously twice daily, or meropenem, 1 g intravenously three times daily for 2 weeks
Then, trimethoprim-sulfamethoxazole 160/800 mg twice daily for 12 months
For patients allergic to sulfonamides or resistant to therapy, consider long-term treatment with doxycycline or hydroxychloroquine
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