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Multifocal hepatic steatosis mimicking malignancy in two siblings

Multifocal hepatic steatosis (MHS) is a rare subtype of hepatic steatosis which can pose a diagnostic challenge due to difficulty in distinguishing it from malignant disease. Steatotic nodules in MHS can vary in size from a few millimeters to several centimeters and may mimic hepatocellular carcinom...

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Detalles Bibliográficos
Autores principales: Freebody, John, Comin, Giulio, Segelov, Eva, Tarlinton, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Publishing Asia Pty Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684502/
https://www.ncbi.nlm.nih.gov/pubmed/31406930
http://dx.doi.org/10.1002/jgh3.12142
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author Freebody, John
Comin, Giulio
Segelov, Eva
Tarlinton, Lisa
author_facet Freebody, John
Comin, Giulio
Segelov, Eva
Tarlinton, Lisa
author_sort Freebody, John
collection PubMed
description Multifocal hepatic steatosis (MHS) is a rare subtype of hepatic steatosis which can pose a diagnostic challenge due to difficulty in distinguishing it from malignant disease. Steatotic nodules in MHS can vary in size from a few millimeters to several centimeters and may mimic hepatocellular carcinoma or metastases by both ultrasound and computed tomography assessment. Accurate detection of this abnormality is important and may prevent unnecessary investigation and biopsy, as well as anxiety for the patient. Here we present two cases of MHS occurring in adult siblings. The characteristic radiographic appearances of MHS will be described as well as tips provided for accurate detection. Given the rarity of this entity, the occurrence in two otherwise well adult siblings also raises the possibility of an inherited pathogenesis.
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spelling pubmed-66845022019-08-12 Multifocal hepatic steatosis mimicking malignancy in two siblings Freebody, John Comin, Giulio Segelov, Eva Tarlinton, Lisa JGH Open Case Reports Multifocal hepatic steatosis (MHS) is a rare subtype of hepatic steatosis which can pose a diagnostic challenge due to difficulty in distinguishing it from malignant disease. Steatotic nodules in MHS can vary in size from a few millimeters to several centimeters and may mimic hepatocellular carcinoma or metastases by both ultrasound and computed tomography assessment. Accurate detection of this abnormality is important and may prevent unnecessary investigation and biopsy, as well as anxiety for the patient. Here we present two cases of MHS occurring in adult siblings. The characteristic radiographic appearances of MHS will be described as well as tips provided for accurate detection. Given the rarity of this entity, the occurrence in two otherwise well adult siblings also raises the possibility of an inherited pathogenesis. Wiley Publishing Asia Pty Ltd 2019-02-11 /pmc/articles/PMC6684502/ /pubmed/31406930 http://dx.doi.org/10.1002/jgh3.12142 Text en © 2019 The Authors. JGH Open: An open access journal of gastroenterology and hepatology published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Case Reports
Freebody, John
Comin, Giulio
Segelov, Eva
Tarlinton, Lisa
Multifocal hepatic steatosis mimicking malignancy in two siblings
title Multifocal hepatic steatosis mimicking malignancy in two siblings
title_full Multifocal hepatic steatosis mimicking malignancy in two siblings
title_fullStr Multifocal hepatic steatosis mimicking malignancy in two siblings
title_full_unstemmed Multifocal hepatic steatosis mimicking malignancy in two siblings
title_short Multifocal hepatic steatosis mimicking malignancy in two siblings
title_sort multifocal hepatic steatosis mimicking malignancy in two siblings
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684502/
https://www.ncbi.nlm.nih.gov/pubmed/31406930
http://dx.doi.org/10.1002/jgh3.12142
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