دورية أكاديمية

Whipple’s Disease: A Rare Cause of Malabsorption Syndrome

التفاصيل البيبلوغرافية
العنوان: Whipple’s Disease: A Rare Cause of Malabsorption Syndrome
المؤلفون: Joana Cardoso, Lídia Gomes, Sandra Santos, Hélder Moreira, Paula Gomes, João Rua, Jorge Fortuna
المصدر: GE: Portuguese Journal of Gastroenterology, Pp 1-7 (2019)
بيانات النشر: Karger Publishers, 2019.
سنة النشر: 2019
المجموعة: LCC:Diseases of the digestive system. Gastroenterology
مصطلحات موضوعية: whipple’s disease, tropheryma whipplei, periodic acid-schiff, Diseases of the digestive system. Gastroenterology, RC799-869
الوصف: Introduction: Whipple’s disease is a rare, chronic, systemic disease caused by the actinomycete Tropheryma whipplei. Clinical manifestations vary widely depending on the affected system, the most common being the digestive tract. Case Presentation: The authors report the case of a 52-year-old man with malabsorption syndrome, diarrhea, marked weight loss, melanoderma, and visual and proprioception disorders. Periodic acid-Schiff staining of a proximal small bowel biopsy and peripheral-blood PCR identification of T. whipplei confirmed the disease. The patient was initially treated with intravenous ceftriaxone, followed by oral trimethoprim/sulfamethoxazole with significant clinical improvement. Conclusions: This case is reported due to its rarity and the diagnostic challenge it presents. Although uncommon, Whipple’s disease should be considered as a differential diagnosis of malabsorption syndrome due to its systemic impact and possible treatment with targeted antibiotic therapy.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2341-4545
2387-1954
العلاقة: https://www.karger.com/Article/FullText/504760Test; https://doaj.org/toc/2341-4545Test; https://doaj.org/toc/2387-1954Test
DOI: 10.1159/000504760
الوصول الحر: https://doaj.org/article/073675fd5a4a48f78e7cf08b5084045dTest
رقم الانضمام: edsdoj.073675fd5a4a48f78e7cf08b5084045d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:23414545
23871954
DOI:10.1159/000504760