Primary Hepatic Mesothelial Cyst: A Rare Entity to Be Considered in the Differential Diagnosis of Neonatal Cystic Lesions.
cd31 negative
congenital hepatic cyst
d2-40
hepatic cyst differential
hepatopathology
mesothelial cyst
neonatal cyst
pediatric surgery
primary hepatic mesothelial cyst
wt1
Journal
Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737
Informations de publication
Date de publication:
Nov 2022
Nov 2022
Historique:
accepted:
04
11
2022
entrez:
7
12
2022
pubmed:
8
12
2022
medline:
8
12
2022
Statut:
epublish
Résumé
We report two cases of primary hepatic mesothelial cysts in neonates previously identified during perinatal imaging. Both neonatal cases were reimaged in the postnatal period, demonstrating the persistence of these cystic hepatic lesions. In both instances, the decision was made to treat with surgical resection and both patients tolerated the surgery well with no significant postoperative complications. Histopathological examination of these lesions discovered a cuboidal lining that was calretinin and WT1 positive and CD31 negative, indicating the diagnosis of a mesothelial cyst of hepatic origin. These cases bring attention to the broad differential diagnosis of congenital primary hepatic cystic lesions, as well as the diagnostic pathway to confirm a primary hepatic mesothelial cyst.
Identifiants
pubmed: 36475178
doi: 10.7759/cureus.31089
pmc: PMC9719715
doi:
Types de publication
Case Reports
Langues
eng
Pagination
e31089Informations de copyright
Copyright © 2022, Gosnell et al.
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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