1. Thrombocytopenia and endocarditis in a patient with Whipple's disease: case report.
- Author
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Olivier M, Licitra C, Field Z, Ge L, Hill D, Madruga M, and Carlan SJ
- Subjects
- Anti-Bacterial Agents therapeutic use, Endocarditis, Bacterial drug therapy, Endocarditis, Bacterial microbiology, Humans, Male, Middle Aged, Platelet Count, Thrombocytopenia drug therapy, Tropheryma pathogenicity, Whipple Disease diagnosis, Endocarditis, Bacterial etiology, Thrombocytopenia etiology, Whipple Disease complications
- Abstract
Background: Whipple's disease (WD) is a rare multisystem infectious disorder that is caused by the actinomycete Tropheryma whipplei. It presents with joint pain followed by abdominal pain, diarrhea, malabsorption and finally failure to thrive. Diagnosis requires tissue sampling and histology with periodic acid-Schiff [PAS] staining. Thrombocytopenia associated with endocarditis associated with WD has been reported twice., Case Presentation: A 56 year old Caucasian male presented with years of steroid treated joint pain and recent onset diarrhea, weight loss and abdominal pain. Ultimately he was found to have a platelet count of 4000 with concomitant endocarditis and embolic stroke. Small bowel biopsy confirmed the diagnosis of WD approximately 1 year after his first visit. His platelets improved with antibiotic treatment but he eventually expired 16 months after his initial consult and 5 months after his definitive diagnosis., Conclusion: WD can remain undiagnosed and untreated until late in the course of the illness. A high index of suspicion is recognized as necessary for early diagnosis to begin treatment. Critical thrombocytopenia associated with endocarditis is a rare and potentially poor prognostic sign in late stage Whipple's disease.
- Published
- 2020
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