Etiology of cirrhosis in the young.


Journal

Human pathology
ISSN: 1532-8392
Titre abrégé: Hum Pathol
Pays: United States
ID NLM: 9421547

Informations de publication

Date de publication:
02 2020
Historique:
received: 21 08 2019
accepted: 10 09 2019
pubmed: 8 11 2019
medline: 15 7 2020
entrez: 8 11 2019
Statut: ppublish

Résumé

The etiology and incidence of cirrhosis in adults has been well studied, however there is scant data in younger patients. The aim of this study was to determine causes of cirrhosis in patients ≤40 years old. In this multi-institutional retrospective study, pathology databases were searched for patients ≤40-year-old with a diagnosis of cirrhosis from 1995 to 2018. Clinical charts and pathology reports were reviewed to identify etiologies of cirrhosis in each case. The patients were divided into 4 age groups (<1, 1- < 5, 5- < 18, and 18-40 years old) for further analysis. We identified 594 patients (264 female, 330 male). Among <18-year-old patients, congenital cholestatic diseases and developmental disorders were the most common causes of cirrhosis (50.2%, 172/342). Metabolic and genetic diseases were also seen more commonly in this age group (16.6%, 57/342). In contrast, viral hepatitides were the most common cause of cirrhosis in 18-40-year-old patients (39.6%, 100/252) followed by autoimmune and fatty liver disease (22.2%, 56/252 and 15.07%, 38/252, respectively). Cryptogenic cirrhosis (overall 7.2%, 42/594) was seen in 3% (4/133), 1.4% (1/69), 10.7% (15/140) and 8.7% (22/252) of patients aged <1, 1- < 5, 5- < 18, and 18-40 years, respectively. Developmental and metabolic disorders are the most common causes of cirrhosis in children (<18), while viral hepatitides are leading causes in adolescents and young adults (18-40) similar to adults. The incidence of cryptogenic cirrhosis also varies depending on the age, being lowest in 1- < 5 year and highest in 5- < 18 year age group children.

Identifiants

pubmed: 31698008
pii: S0046-8177(19)30194-7
doi: 10.1016/j.humpath.2019.09.015
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

96-103

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Maria C Olave (MC)

Yale University School of Medicine, Department of Pathology, New Haven, CT 06511, United States. Electronic address: maria.olave-martinez@yale.edu.

Ananta Gurung (A)

Yale University School of Medicine, Department of Pathology, New Haven, CT 06511, United States; Department of Pathology, Royal Columbian Hospital, New Westminster, BC 3W7, Canada. Electronic address: Ananta.Gurung@fraserhealth.ca.

Pramod K Mistry (PK)

Yale University School of Medicine, Department of Internal Medicine, New Haven, CT 3W7, United States. Electronic address: pramod.mistry@yale.edu.

Sanjay Kakar (S)

University of California, San Francisco, Department of Pathology, San Francisco, CA 3W7, United States. Electronic address: pramod.mistry@yale.edu.

Matthew Yeh (M)

University of Washington, Department of Pathology, Seattle, WA 3W7, United States. Electronic address: pramod.mistry@yale.edu.

Min Xu (M)

Department of Pathology, Seattle Children's Hospital, and Department of Laboratory Medicine, University of Washington School of Medicine, Seattle 3W7. Electronic address: pramod.mistry@yale.edu.

Tsung-Teh Wu (TT)

Mayo Clinic, Division of Pathology, Rochester, MN 3W7, United States. Electronic address: pramod.mistry@yale.edu.

Michael Torbenson (M)

Mayo Clinic, Division of Pathology, Rochester, MN 3W7, United States. Electronic address: pramod.mistry@yale.edu.

Dhanpat Jain (D)

Yale University School of Medicine, Department of Pathology, New Haven, CT 06511, United States. Electronic address: pramod.mistry@yale.edu.

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