Atypical Whipple's disease with special endoscopic manifestations: A case report

Whipple's disease is a rare systemic infection caused by . Most patients present with nonspecific symptoms, and routine laboratory and imaging examination results also lack specificity. The diagnosis often relies on invasive manipulation, pathological examination, and molecular techniques. Thes...

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Published inWorld journal of clinical cases Vol. 10; no. 35; pp. 13044 - 13051
Main Authors Chen, Shuo, Zhou, Yuan-Chen, Si, Shuang, Liu, Hong-Yan, Zhang, Qing-Rui, Yin, Teng-Fei, Xie, Chu-Xi, Yao, Shu-Kun, Du, Shi-Yu
Format Journal Article
LanguageEnglish
Published United States Baishideng Publishing Group Inc 16.12.2022
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Summary:Whipple's disease is a rare systemic infection caused by . Most patients present with nonspecific symptoms, and routine laboratory and imaging examination results also lack specificity. The diagnosis often relies on invasive manipulation, pathological examination, and molecular techniques. These difficulties in diagnosing Whipple's disease often result in misdiagnosis and inappropriate treatments. This paper reports on the case of a 58-year-old male patient who complained of fatigue and decreased exercise capacity. The results of routine blood tests indicated hypochromic microcytic anemia. Results of gastroscopy and capsule endoscopy showed multiple polypoid bulges distributed in the duodenal and proximal jejunum. A diagnosis of small intestinal adenomatosis was initially considered; hence, the Whipple procedure, a pylorus-preserving pancreaticoduodenectomy, was performed. Pathological manifestations showed many periodic acid-Schiff-positive macrophages aggregated in the intestinal mucosa of the duodenum, upper jejunum, and surrounding lymph nodes. Based on comprehensive analysis of symptoms, laboratory findings, and pathological manifestations, the patient was finally diagnosed with Whipple's disease. After receiving 1 mo of antibiotic treatment, the fatigue and anemia were significantly improved. This case presented with atypical gastrointestinal manifestations and small intestinal polypoid bulges, which provided new insight on the diagnosis of Whipple's disease.
Bibliography:Supported by The China-Japan Friendship Hospital Foundation, No. 2019-1-QN-2.
Author contributions: Chen S, Zhou YC, Zhang QR, and Yin TF wrote the main manuscript text under the guidance of Du SY and Yao SK; Si S, Liu HY, and Xie CX prepared the figures; all authors have read and approved the final manuscript.
Corresponding author: Shi-Yu Du, MD, PhD, Chief Physician, Professor, Department of Gastroenterology, China-Japan Friendship Hospital, No. 2 Yinghua East Road, Chaoyang District, Beijing 100029, China. shiyudu1975@163.com
ISSN:2307-8960
2307-8960
DOI:10.12998/wjcc.v10.i35.13044