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Whipple's disease: rare disorder and late diagnosis

By Viviane Plasse Renon, Marcelo Campos Appel-da-Silva, Rafael Bergesch D'Incao, Rodrigo Mayer Lul, Luciana Schmidt Kirschnick and Bruno Galperim

Abstract

Whipple's disease is a rare systemic infectious disorder caused by the bacterium Tropheryma whipplei. We report the case of a 61-year-old male patient who presented to emergency room complaining of asthenia, arthralgia, anorexia, articular complaints intermittent diarrhea, and a 10-kg weight loss in one year. Laboratory tests showed the following results: Hb = 7.5 g/dL, albumin = 2.5 mg/dL, weight = 50.3 kg (BMI 17.4 kg/m²). Upper gastrointestinal endoscopy revealed areas of focal enanthema in the duodenum. An endoscopic biopsy was suggestive of Whipple's disease. Diagnosis was confirmed based on a positive serum polymerase chain reaction. Treatment was initiated with intravenous ceftriaxone followed by oral trimethoprim-sulfamethoxazole. After one year of treatment, the patient was asymptomatic, with Hb = 13.5 g/dL, serum albumin = 5.3 mg/dL, and weight = 70 kg (BMI 24.2 kg/m²). Whipple's disease should be considered a differential diagnosis in patients with prolonged constitutional and/or gastrointestinal symptoms. Appropriate antibiotic treatment improves the quality of life of patients

Topics: Whipple's disease, Tropheryma whipplei, Malabsorption syndromes, Medicine (General), R5-920, Medicine, R, Arctic medicine. Tropical medicine, RC955-962
Publisher: Universidade de São Paulo
Year: 2012
DOI identifier: 10.1590/S0036-46652012000500010
OAI identifier: oai:doaj.org/article:4741e7cf6d8145c8b3b40071c2d2412f
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