臨床症例報告ジャーナル

Whipple’s Disease in Western Amazonia

Abstract

Gabriel Mendes Picanço*, Yanna Queiroz Pereira de Sá, Ketlin Batista de Morais Mendes, Ananda Castro Chaves Ale, Yanna Queiroz Pereira de Sá, Arlene dos Santos Pinto, Yanna Queiroz Pereira de Sá, Arlene dos Santos Pinto, André Nazário de Oliveira, Antonio Solon Mendes Pereira, Cristhenise Ragnini Silva, Antonio Solon Mendes Pereira

The present article reports a case of Whipple's disease as a rare cause of intestinal malabsorption syndrome, in a young individual with G6PD deficiency and hypothyroidism, without previous follow-up. The male patient initially complained of diarrhea and long-standing weight loss. The complementary examination findings were consistent with Whipple's Disease. Antibiotic therapy (Ceftriaxone) was initiated with subsequent clinical improvement. Although rare, this disease should be considered as a differential diagnosis in patients with intestinal malabsorption, especially considering the systemic impact of the disease and the possible control with appropriate antibiotic therapy.