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Hepatic Sclerosed Hemangioma: a case report and review of the literature

BACKGROUND: Although cavernous hemangioma is one of the most frequently encountered benign hepatic neoplasms, hepatic sclerosed hemangioma is very rare. We report a case of hepatic sclerosed hemangioma that was difficult to distinguish from an intrahepatic cholangiocarcinoma by imaging studies. CASE...

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Autores principales: Miyamoto, Shunsuke, Oshita, Akihiko, Daimaru, Yutaka, Sasaki, Masaru, Ohdan, Hideki, Nakamitsu, Atsushi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428228/
https://www.ncbi.nlm.nih.gov/pubmed/25927893
http://dx.doi.org/10.1186/s12893-015-0029-x
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author Miyamoto, Shunsuke
Oshita, Akihiko
Daimaru, Yutaka
Sasaki, Masaru
Ohdan, Hideki
Nakamitsu, Atsushi
author_facet Miyamoto, Shunsuke
Oshita, Akihiko
Daimaru, Yutaka
Sasaki, Masaru
Ohdan, Hideki
Nakamitsu, Atsushi
author_sort Miyamoto, Shunsuke
collection PubMed
description BACKGROUND: Although cavernous hemangioma is one of the most frequently encountered benign hepatic neoplasms, hepatic sclerosed hemangioma is very rare. We report a case of hepatic sclerosed hemangioma that was difficult to distinguish from an intrahepatic cholangiocarcinoma by imaging studies. CASE PRESENTATION: A 76-year-old male patient with right hypochondralgia was referred to our hospital. Abdominal ultrasonography revealed a heterogeneously hyperechoic tumor that was 59 mm in diameter in segment 7 of the liver. Dynamic computed tomography showed a low-density tumor with delayed ring enhancement. Gadolinium-ethoxybenzyl-diethylenetriamine pentaacetic acid-enhanced magnetic resonance imaging (EOB-MRI) demonstrated a low-signal intensity mass with ring enhancement on T1-weighted images. The mass had several high-signal intensity lesions on T2-weighted images. EOB-MRI revealed a hypointense nodule on the hepatobiliary phase. From these imaging studies, the tumor was diagnosed as intrahepatic cholangiocarcinoma, and we performed laparoscopy-assisted posterior sectionectomy of the liver with lymph node dissection in the hepatoduodenal ligament. Histopathological examination revealed a hepatic sclerosed hemangioma with hyalinized tissue and collagen fibers. CONCLUSION: Hepatic sclerosed hemangioma is difficult to diagnose preoperatively because of its various imaging findings. We report a case of hepatic sclerosed hemangioma and review the literatures, especially those concerning imaging findings.
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spelling pubmed-44282282015-05-13 Hepatic Sclerosed Hemangioma: a case report and review of the literature Miyamoto, Shunsuke Oshita, Akihiko Daimaru, Yutaka Sasaki, Masaru Ohdan, Hideki Nakamitsu, Atsushi BMC Surg Case Report BACKGROUND: Although cavernous hemangioma is one of the most frequently encountered benign hepatic neoplasms, hepatic sclerosed hemangioma is very rare. We report a case of hepatic sclerosed hemangioma that was difficult to distinguish from an intrahepatic cholangiocarcinoma by imaging studies. CASE PRESENTATION: A 76-year-old male patient with right hypochondralgia was referred to our hospital. Abdominal ultrasonography revealed a heterogeneously hyperechoic tumor that was 59 mm in diameter in segment 7 of the liver. Dynamic computed tomography showed a low-density tumor with delayed ring enhancement. Gadolinium-ethoxybenzyl-diethylenetriamine pentaacetic acid-enhanced magnetic resonance imaging (EOB-MRI) demonstrated a low-signal intensity mass with ring enhancement on T1-weighted images. The mass had several high-signal intensity lesions on T2-weighted images. EOB-MRI revealed a hypointense nodule on the hepatobiliary phase. From these imaging studies, the tumor was diagnosed as intrahepatic cholangiocarcinoma, and we performed laparoscopy-assisted posterior sectionectomy of the liver with lymph node dissection in the hepatoduodenal ligament. Histopathological examination revealed a hepatic sclerosed hemangioma with hyalinized tissue and collagen fibers. CONCLUSION: Hepatic sclerosed hemangioma is difficult to diagnose preoperatively because of its various imaging findings. We report a case of hepatic sclerosed hemangioma and review the literatures, especially those concerning imaging findings. BioMed Central 2015-04-17 /pmc/articles/PMC4428228/ /pubmed/25927893 http://dx.doi.org/10.1186/s12893-015-0029-x Text en © Miyamoto et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Miyamoto, Shunsuke
Oshita, Akihiko
Daimaru, Yutaka
Sasaki, Masaru
Ohdan, Hideki
Nakamitsu, Atsushi
Hepatic Sclerosed Hemangioma: a case report and review of the literature
title Hepatic Sclerosed Hemangioma: a case report and review of the literature
title_full Hepatic Sclerosed Hemangioma: a case report and review of the literature
title_fullStr Hepatic Sclerosed Hemangioma: a case report and review of the literature
title_full_unstemmed Hepatic Sclerosed Hemangioma: a case report and review of the literature
title_short Hepatic Sclerosed Hemangioma: a case report and review of the literature
title_sort hepatic sclerosed hemangioma: a case report and review of the literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428228/
https://www.ncbi.nlm.nih.gov/pubmed/25927893
http://dx.doi.org/10.1186/s12893-015-0029-x
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