Another Whipple's triad? Pericardial, myocardial and valvular disease in an unusual case presentation from a Canadian perspective

• Published in: BMC cardiovascular disorders 2019-12, Vol.19 (1), p.312-312, Article 312
• Main Authors: Thornton, Christina S, Wang, Yinong, Köebel, Martin, Bernard, Kathryn, Burdz, Tamara, Maitland, Andrew, Ferraz, Jose G, Beck, Paul L, Ferland, Andre
• Format: Article
• Language: English
• Subjects: Biopsy; Calcification; Case Report; Congestive heart failure; Culture-negative infective endocarditis; Diagnosis; Endocarditis; Epidemiology; Family medical history; Fatigue; Heart failure; Heart surgery; Heart valve diseases; Infective endocarditis; Literature reviews; Penicillin G; Pericarditis; Physiology; rRNA 16S; Stains & staining; Surgery; Tropheryma whipplei; Ultrasonic imaging; Whipple's disease
• ISSN: 1471-2261; 1471-2261
• DOI: 10.1186/s12872-019-1257-2

Whipple's disease is a clinically relevant multi-system disorder that is often undiagnosed given its elusive nature. We present an atypical case of Whipple's disease involving pan-valvular endocarditis and constrictive pericarditis, requiring cardiac intervention. A literature review was also performed assessing the prevalence of atypical cases of Whipple's disease. A previously healthy 56-year-old male presented with a four-year history of congestive heart failure with weight loss and fatigue. Notably, he had absent gastrointestinal symptoms. He went on to develop pan-valvular endocarditis and constrictive pericarditis requiring urgent cardiac surgery. A clinical diagnosis of Whipple's disease was suspected, prompting duodenal biopsy sampling which was unremarkable, Subsequently, Tropheryma whipplei was identified by 16S rDNA PCR on the cardiac valvular tissue. He underwent prolonged antibiotic therapy with recovery of symptoms. Our study reports the first known case of Whipple's disease involving pan-valvular endocarditis and constrictive pericarditis. A literature review also highlights this presentation of atypical Whipple's with limited gastrointestinal manifestations. Duodenal involvement was limited and the gold standard of biopsy was not contributory. We also highlight the Canadian epidemiology of the disease from 2012 to 2016 with an approximate 4% prevalence rate amongst submitted samples. Routine investigations for Whipple's disease, including duodenal biopsy, in this case may have missed the diagnosis. A high degree of suspicion was critical for diagnosis of unusual manifestations of Whipple's disease.