AI Article Synopsis

  • A case study is presented involving a girl with 21trisomy who experienced severe anemia and chronic ileum obstruction, ultimately requiring surgical intervention, which led to her recovery.
  • After surgery, tests showed improvements in her condition, suggesting a link between her GI inflammation and the underlying immunological and gastrointestinal challenges associated with 21trisomy.

Article Abstract

Patients with 21trisomy often develop congenital or acquired gastrointestinal diseases, such as duodenal or anal atresia, celiac disease, intussusception, and constipation. In these patients, it is often challenging to diagnose gastrointestinal diseases because most patients have difficulty explaining their complaints in detail. Furthermore, these patients also possess immunological disorders, such as increased type I interferon activation, innate immune hypersensitivity, and polarization to autoimmune. Here, we present a girl with 21trisomy and constipation who developed severe anemia, occult blood and elevated levels of calprotectin in stool, and chronic ileum obstruction confirmed by computed tomography. The patient underwent surgical resection of the ileum and recovered without complications. Pathological examination demonstrated intussusception, ischemia, ulceration, inflammatory granulation, and massive IgG4-positive plasma cell infiltration. After the surgery, her fecal calprotectin levels were normalized. We assumed that the ileum inflammation caused by ileum dilation generated ulcers and granulation, which could be associated with immunological, gastrointestinal, and intellectual disorders in patients with 21trisomy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11167512PMC
http://dx.doi.org/10.7759/cureus.60177DOI Listing

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