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More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess

Hepatic angiomyolipomas (AML) are rare mesenchymal tumours of which the epithelioid type is a rare type with malignant potential. We report a case of primary hepatic epithelioid angiomyolipoma masquerading as liver abscess. A 46-year-old man presented with a 5-day history of fever with epigastric pa...

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Autores principales: Leong, Wen Hao Justin, Tan, Xia Huang Andrew, Salazar, Ennaliza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879258/
https://www.ncbi.nlm.nih.gov/pubmed/33613156
http://dx.doi.org/10.1159/000511886
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author Leong, Wen Hao Justin
Tan, Xia Huang Andrew
Salazar, Ennaliza
author_facet Leong, Wen Hao Justin
Tan, Xia Huang Andrew
Salazar, Ennaliza
author_sort Leong, Wen Hao Justin
collection PubMed
description Hepatic angiomyolipomas (AML) are rare mesenchymal tumours of which the epithelioid type is a rare type with malignant potential. We report a case of primary hepatic epithelioid angiomyolipoma masquerading as liver abscess. A 46-year-old man presented with a 5-day history of fever with epigastric pain and nausea. On the night of admission, his temperature spiked to 39°C, his blood pressure was 135/79, his heart rate 98, his liver function test revealed albumin 37 g/L, bilirubin 25 μmol/L, ALP 298 U/L, ALT 247 U/L, and AST 344 U/L. The clinical suspicion was hepatobiliary sepsis and intravenous ceftriaxone was commenced. CT of the abdomen showed an ill-defined hypodense focus in segment 4A/8 (4.5 × 3.5 cm) with a minimal fluid component implying a developing abscess or phlegmon. The images were reviewed by a radiologist and showed minimal fluid for percutaneous drainage. MRI of the liver was performed to further characterize the lesion and revealed a solid mass with nodular areas of arterial enhancement and washout, suspicious of neoplasm. Ultrasound-guided liver biopsy of the lesion was performed. Histology showed a histiocyte-rich epithelioid neoplasm consistent with the epithelioid variant of AML. Immunohistochemical staining was positive for human melanoma black 45, melan-A and cluster of differentiation 68. He successfully underwent liver resection of segment 4A/8 after 6 weeks of antibiotics. To our knowledge, this is the first reported case in the literature of primary hepatic epithelioid angiomyolipoma masquerading as liver abscess.
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spelling pubmed-78792582021-02-18 More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess Leong, Wen Hao Justin Tan, Xia Huang Andrew Salazar, Ennaliza Case Rep Gastroenterol Single Case Hepatic angiomyolipomas (AML) are rare mesenchymal tumours of which the epithelioid type is a rare type with malignant potential. We report a case of primary hepatic epithelioid angiomyolipoma masquerading as liver abscess. A 46-year-old man presented with a 5-day history of fever with epigastric pain and nausea. On the night of admission, his temperature spiked to 39°C, his blood pressure was 135/79, his heart rate 98, his liver function test revealed albumin 37 g/L, bilirubin 25 μmol/L, ALP 298 U/L, ALT 247 U/L, and AST 344 U/L. The clinical suspicion was hepatobiliary sepsis and intravenous ceftriaxone was commenced. CT of the abdomen showed an ill-defined hypodense focus in segment 4A/8 (4.5 × 3.5 cm) with a minimal fluid component implying a developing abscess or phlegmon. The images were reviewed by a radiologist and showed minimal fluid for percutaneous drainage. MRI of the liver was performed to further characterize the lesion and revealed a solid mass with nodular areas of arterial enhancement and washout, suspicious of neoplasm. Ultrasound-guided liver biopsy of the lesion was performed. Histology showed a histiocyte-rich epithelioid neoplasm consistent with the epithelioid variant of AML. Immunohistochemical staining was positive for human melanoma black 45, melan-A and cluster of differentiation 68. He successfully underwent liver resection of segment 4A/8 after 6 weeks of antibiotics. To our knowledge, this is the first reported case in the literature of primary hepatic epithelioid angiomyolipoma masquerading as liver abscess. S. Karger AG 2021-01-08 /pmc/articles/PMC7879258/ /pubmed/33613156 http://dx.doi.org/10.1159/000511886 Text en Copyright © 2021 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Single Case
Leong, Wen Hao Justin
Tan, Xia Huang Andrew
Salazar, Ennaliza
More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
title More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
title_full More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
title_fullStr More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
title_full_unstemmed More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
title_short More than Pus − Primary Hepatic Epithelioid Angiomyolipoma Masquerading as Liver Abscess
title_sort more than pus − primary hepatic epithelioid angiomyolipoma masquerading as liver abscess
topic Single Case
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7879258/
https://www.ncbi.nlm.nih.gov/pubmed/33613156
http://dx.doi.org/10.1159/000511886
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