Skip to content
DraconiticResearch
Search Sources API
203,948 studies31 sourcesUpdated 39 min ago
Peer-reviewedCC BY 4.0JPGN Reports

Multi‐segment intussusception in infant with suspected celiac crisis: A case report

  1. 1Department of Pediatrics University of California, San Francisco Oakland California USA
  2. 2Department of Pathology University of California, San Francisco San Francisco California USA

Abstract

Celiac crisis (CC) is a rare, life‐threatening manifestation of often undiagnosed or inadequately treated celiac disease (CeD). In infants with nonclassical presentations of CeD, timely diagnosis can be challenging but critical to reducing end‐organ damage and serious complications, such as CC. We report a case of a 14‐month‐old infant presenting with 1 month of inappetence, malnutrition, and abdominal pain in the absence of diarrhea. The infant was found to have extraintestinal manifestations suggestive of CC, such as electrolyte derangement, hypoalbuminemia, and neurologic dysfunction. However, the infant also presented with unusual multi‐segment small bowel‐small bowel intussusception prior to the diagnosis of CeD. Intussusception may reflect severe small bowel enteropathy in CeD. Hypoalbuminemia and intestinal edema seen in CC may further precipitate small bowel‐small bowel intussusception. Future studies should clarify distinct phenotypes of infantile‐onset CeD associated with more severe CC.

Related

  1. Inferolateral ST-Segment Elevation Myocardial Infarction Secondary to Suspected Coronary Embolism in a Patient with Paroxysmal Atrial Fibrillation: A Case Report.
    Sai Tharun Reddy Gopannagari, Kesava Manikanta Achuta, Ishan Kirti +2
    International medical case reports journalPeer-reviewedCC BY-NCFull textCardiovascular medicineEurope PMC
  2. Giant congenital lymphedema in an infant with suspected milroy disease (hereditary lymphedema type IA): a case report
    Yoyos Dias Ismiarto, Teuku Aditya Kemal, Sudaryanto +2
    Frontiers in surgeryPeer-reviewedCC BYFull textOncologyEurope PMCEurope PMCPMC
  3. Suspected donor-vessel ischemia in a collateral-dependent right coronary artery occlusion presenting as a de Winter-like pattern with inferior ST-segment elevation: a case report
    Zhihao Liu, Leyi Wang, Yan Zhang +1
    BMC Cardiovascular DisordersPeer-reviewedCC BY-NC-ND 4.0Full textCardiovascular medicinePMC
  4. Infant-onset mevalonate kinase deficiency with a previously unreported MVK c.827 A > G (p.Glu276Gly) variant presenting as suspected incomplete kawasaki disease with marked hyperinflammation: clinical response to firsekibart and systematic evidence synthesis
    Yang Shen, Yutong Gao, Jing Shan +7
    Pediatric RheumatologyPeer-reviewedCC BY-NC-ND 4.0Full textObstetrics, gynaecology & paediatricsPMC
  5. Jejunal intussusception following distal gastrectomy with Billroth I anastomosis: a case report
    Jing Guo, Runjie Hou, Yuan Zhang +3
    Frontiers in surgeryPeer-reviewedCC BYFull textSurgery & anaesthesiaEurope PMC
BibTeX
@article{thakur2026multisegment,
  title = {{Multi‐segment intussusception in infant with suspected celiac crisis: A case report}},
  author = {Shambhawi Thakur and Angela Tran and Vivien Nguyen and Soo‐Jin Cho and Telly Cheung},
  journal = {JPGN Reports},
  year = {2026},
  month = nov,
  doi = {10.1002/jpr3.70269},
  url = {https://doi.org/10.1002/jpr3.70269},
  note = {CC BY 4.0},
}
RIS
TY  - JOUR
TI  - Multi‐segment intussusception in infant with suspected celiac crisis: A case report
AU  - Shambhawi Thakur
AU  - Angela Tran
AU  - Vivien Nguyen
AU  - Soo‐Jin Cho
AU  - Telly Cheung
PY  - 2026
DA  - 2026/11/05
JO  - JPGN Reports
DO  - 10.1002/jpr3.70269
UR  - https://doi.org/10.1002/jpr3.70269
AB  - Celiac crisis (CC) is a rare, life‐threatening manifestation of often undiagnosed or inadequately treated celiac disease (CeD). In infants with nonclassical presentations of CeD, timely diagnosis can be challenging but critical to reducing end‐organ damage and serious complications, such as CC. We report a case of a 14‐month‐old infant presenting with 1 month of inappetence, malnutrition, and abdominal pain in the absence of diarrhea. The infant was found to have extraintestinal manifestations suggestive of CC, such as electrolyte derangement, hypoalbuminemia, and neurologic dysfunction. However, the infant also presented with unusual multi‐segment small bowel‐small bowel intussusception prior to the diagnosis of CeD. Intussusception may reflect severe small bowel enteropathy in CeD. Hypoalbuminemia and intestinal edema seen in CC may further precipitate small bowel‐small bowel intussusception. Future studies should clarify distinct phenotypes of infantile‐onset CeD associated with more severe CC.
SN  - 2691-171X
ER  -