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Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis
BACKGROUND: Hepatic epithelioid angiomyolipoma (HEAML) is a rare liver disease and is easily misdiagnosed. Enhanced recognition of HEAML is beneficial to the differential diagnosis of rare liver diseases. CASE SUMMARY: We presented two cases of HEAML in Changzheng Hospital, Naval Medical University,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509262/ https://www.ncbi.nlm.nih.gov/pubmed/31119142 http://dx.doi.org/10.12998/wjcc.v7.i8.972 |
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author | Mao, Jia-Xi Teng, Fei Liu, Cong Yuan, Hang Sun, Ke-Yan Zou, You Dong, Jia-Yong Ji, Jun-Song Dong, Jun-Feng Fu, Hong Ding, Guo-Shan Guo, Wen-Yuan |
author_facet | Mao, Jia-Xi Teng, Fei Liu, Cong Yuan, Hang Sun, Ke-Yan Zou, You Dong, Jia-Yong Ji, Jun-Song Dong, Jun-Feng Fu, Hong Ding, Guo-Shan Guo, Wen-Yuan |
author_sort | Mao, Jia-Xi |
collection | PubMed |
description | BACKGROUND: Hepatic epithelioid angiomyolipoma (HEAML) is a rare liver disease and is easily misdiagnosed. Enhanced recognition of HEAML is beneficial to the differential diagnosis of rare liver diseases. CASE SUMMARY: We presented two cases of HEAML in Changzheng Hospital, Naval Medical University, and then collected and analyzed all reports about HEAML recorded in PubMed, MEDLINE, China Science Periodical Database, and VIP database from January 2000 to March 2018. A total of 409 cases of HEAML in 97 reports were collected, with a ratio of men to women of 1:4.84 and an age range from 12 years to 80 years (median 44 years). Among the patients with clinical symptoms mentioned, 61.93% (205/331) were asymptomatic, 34.74% (115/331) showed upper or right upper quadrant abdomen discomfort, while a few of them showed abdominal mass, gastrointestinal symptoms, low fever, or weight loss. The misdiagnosis rate of HEAML was as high as 40.34% (165/409) due to its nonspecific imaging findings. Most of the tumors were solitary and round in morphology, with clear boundaries. Ultrasound scan indicated low echo with internal nonuniformity and rich blood supply in most cases. Computer tomography/magnetic resonance imaging enhanced scan showed varied characteristics. The ratio of fast wash-in and fast wash-out, fast wash-in and slow wash-out, and delayed enhancement was roughly 4:5:1. A definite diagnosis of HEAML depended on the pathological findings of the epithelioid cells in lesions and the expression of human melanoma black 45, smooth muscle actin, melanoma antigen, and actin by immunohistochemical staining. HEAML had a relatively low malignant rate of 3.91%. However, surgical resection was the main treatment for HEAML, due to the difficulty diagnosing before operation. CONCLUSION: HEAML is a rare and easily misdiagnosed disease, and it should be diagnosed carefully, taking into account clinical course, imaging, pathological ,and immunohistochemical findings. |
format | Online Article Text |
id | pubmed-6509262 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-65092622019-05-22 Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis Mao, Jia-Xi Teng, Fei Liu, Cong Yuan, Hang Sun, Ke-Yan Zou, You Dong, Jia-Yong Ji, Jun-Song Dong, Jun-Feng Fu, Hong Ding, Guo-Shan Guo, Wen-Yuan World J Clin Cases Case Report BACKGROUND: Hepatic epithelioid angiomyolipoma (HEAML) is a rare liver disease and is easily misdiagnosed. Enhanced recognition of HEAML is beneficial to the differential diagnosis of rare liver diseases. CASE SUMMARY: We presented two cases of HEAML in Changzheng Hospital, Naval Medical University, and then collected and analyzed all reports about HEAML recorded in PubMed, MEDLINE, China Science Periodical Database, and VIP database from January 2000 to March 2018. A total of 409 cases of HEAML in 97 reports were collected, with a ratio of men to women of 1:4.84 and an age range from 12 years to 80 years (median 44 years). Among the patients with clinical symptoms mentioned, 61.93% (205/331) were asymptomatic, 34.74% (115/331) showed upper or right upper quadrant abdomen discomfort, while a few of them showed abdominal mass, gastrointestinal symptoms, low fever, or weight loss. The misdiagnosis rate of HEAML was as high as 40.34% (165/409) due to its nonspecific imaging findings. Most of the tumors were solitary and round in morphology, with clear boundaries. Ultrasound scan indicated low echo with internal nonuniformity and rich blood supply in most cases. Computer tomography/magnetic resonance imaging enhanced scan showed varied characteristics. The ratio of fast wash-in and fast wash-out, fast wash-in and slow wash-out, and delayed enhancement was roughly 4:5:1. A definite diagnosis of HEAML depended on the pathological findings of the epithelioid cells in lesions and the expression of human melanoma black 45, smooth muscle actin, melanoma antigen, and actin by immunohistochemical staining. HEAML had a relatively low malignant rate of 3.91%. However, surgical resection was the main treatment for HEAML, due to the difficulty diagnosing before operation. CONCLUSION: HEAML is a rare and easily misdiagnosed disease, and it should be diagnosed carefully, taking into account clinical course, imaging, pathological ,and immunohistochemical findings. Baishideng Publishing Group Inc 2019-04-26 2019-04-26 /pmc/articles/PMC6509262/ /pubmed/31119142 http://dx.doi.org/10.12998/wjcc.v7.i8.972 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Case Report Mao, Jia-Xi Teng, Fei Liu, Cong Yuan, Hang Sun, Ke-Yan Zou, You Dong, Jia-Yong Ji, Jun-Song Dong, Jun-Feng Fu, Hong Ding, Guo-Shan Guo, Wen-Yuan Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis |
title | Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis |
title_full | Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis |
title_fullStr | Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis |
title_full_unstemmed | Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis |
title_short | Two case reports and literature review for hepatic epithelioid angiomyolipoma: Pitfall of misdiagnosis |
title_sort | two case reports and literature review for hepatic epithelioid angiomyolipoma: pitfall of misdiagnosis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509262/ https://www.ncbi.nlm.nih.gov/pubmed/31119142 http://dx.doi.org/10.12998/wjcc.v7.i8.972 |
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