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New Findings of Immunodysregulation, Polyendocrinopathy, and Enteropathy X-linked Syndrome (IPEX); Granulomas in Lung and Duodenum.

Demet Teker DuztasLina Al-ShadfanHakan OzturkHakan YazanErkan CakirNurcan Unver Ozgur EkinciBuket DalgicMeino RohlfsTim JeskeChristoph KleinDaniel KotlarzOdul Egritas Gurkan
Published in: Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society (2021)
Immune dysregulation, polyendocrinopathy and enteropathy, X-linked (IPEX) syndrome is a rare disorder caused by loss-of-function mutations in the gene forkhead box protein 3 (FOXP3). IPEX patients frequently show chronic diarrhea (enteropathy) associated with villous atrophies in the small intestine. Our case is different from this classical information in the literature, since he presented with neonatal onset inflammatory bowel disease within the first months of life accompanied by deep ulcers throughout colonic mucosa. Moreover, he developed chronic lung disease during follow-up and histopathological examinations showed granulomas in both gastrointestinal tract and lung parenchyma. Genetic analysis revealed the diagnosis of IPEX syndrome with a germline mutation in FOXP3. Thus, our study provides an unusual presentation of IPEX syndrome with colitis and granulomas presence in histopathological examinations.
Keyphrases
  • case report
  • regulatory t cells
  • transcription factor
  • systematic review
  • newly diagnosed
  • prognostic factors
  • ulcerative colitis
  • chronic kidney disease
  • dna repair
  • dendritic cells
  • dna methylation
  • drug induced