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Autoimmune Liver Diseases in Children
- Source :
- Pediatric Annals. 47
- Publication Year :
- 2018
- Publisher :
- SLACK, Inc., 2018.
-
Abstract
- Autoimmune liver disease remains difficult to diagnose, and distinguishing the various causes is difficult as well. In children, it can present with wide variation, including autoimmune hepatitis (AIH), primary sclerosing cholangitis (PSC), and the “overlap syndrome” of AIH/PSC, also known as autoimmune sclerosing cholangitis. These liver disorders are thought to be immune-mediated, but their etiology remains unclear. They are not secondary to inherited or acquired diseases and they are not associated with any drugs, so they can only be diagnosed if these other diseases or conditions are excluded. Because there is considerable commonality in the clinical presentation of these diseases but differences in their management, appropriate treatment may be delayed, increasing the risk for liver transplantation. Further education for general pediatricians and trainees is needed. This article reviews the differences between AIH and PSC, as well as the newly recognized overlap syndrome of both of these diseases. [ Pediatr Ann. 2018;47(11):e452–e457.]
- Subjects :
- medicine.medical_specialty
Acquired diseases
Adolescent
medicine.medical_treatment
Cholangitis, Sclerosing
Autoimmune hepatitis
Liver transplantation
Primary sclerosing cholangitis
Diagnosis, Differential
03 medical and health sciences
0302 clinical medicine
Humans
Medicine
Child
Autoimmune liver disease
business.industry
Ursodeoxycholic Acid
Endoscopy
Overlap syndrome
medicine.disease
Dermatology
digestive system diseases
Liver Transplantation
Hepatitis, Autoimmune
Liver
030220 oncology & carcinogenesis
Pediatrics, Perinatology and Child Health
Etiology
030211 gastroenterology & hepatology
business
Immunosuppressive Agents
Subjects
Details
- ISSN :
- 19382359 and 00904481
- Volume :
- 47
- Database :
- OpenAIRE
- Journal :
- Pediatric Annals
- Accession number :
- edsair.doi.dedup.....e544205b904b73572893ee1b1f1c052e
- Full Text :
- https://doi.org/10.3928/19382359-20181022-02