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Purpose: To report a case of bilateral anterior uveitis, pigmentary retinopathy, and pars plana exudates in a patient with Celiac disease with complete resolution of inflammation following gluten-free diet.

Methods: Retrospective case report.

Results: A 19-year-old Asian Indian girl presented with bilateral non-granulomatous anterior uveitis for the past 2 months.

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Unlabelled: Crohn's disease (CD) is a transmural inflammatory process that can affect any segment of the gastrointestinal tract. CD has a predilection for the colon and the small bowel, specifically the terminal ileum. Esophageal involvement of CD is exceedingly rare and there is a paucity of data regarding the disease phenotypes, course, complications and treatment.

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A rare case of Whipple disease presenting as a hydrosalpinx and granulomatous peritonitis.

J Infect Dev Ctries

August 2024

Department for Gastroenterology, Military Medical Academy, Belgrade, Serbia.

Article Synopsis
  • Whipple disease, caused by the bacterium Tropheryma whipplei, is a rare infection that primarily impacts the gastrointestinal and musculoskeletal systems but can also affect the heart, brain, and lungs, making diagnosis difficult due to varied symptoms.
  • A case study of a young woman revealed miliary lesions in the pelvis during laparoscopy, initially leading to a diagnosis of granulomatous salpingitis and peritonitis, but ultimately, Tropheryma whipplei was identified as the cause.
  • Timely and appropriate antibiotic treatment is crucial for a positive outcome in Whipple disease, emphasizing the need for increased awareness among healthcare professionals.
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Article Synopsis
  • * Histopathological analysis indicated chronic inflammation and granuloma formation, leading to a preliminary diagnosis of isolated upper GI Crohn's disease.
  • * Further tests showed high levels of IgG4, leading to a conclusion of overlapping IgG4-related disease and Crohn's, which was treated successfully with steroids and anti-TNF therapy.
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Background: Chronic granulomatous disease (CGD) is a rare disorder normally diagnosed in infancy.

Case Presentation: A 27-year-old man admitted with non-specific symptoms of CGD first underwent endoscopy, and colonoscopy procedures as primary evaluation of clinical presentation. Eighteen months after the first admission, he was referred to the emergency department for hematemesis, and critical situations, such as a severe anemic with Hgb= 2.

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