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©The Author(s) 2015. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Aug 28, 2015; 21(32): 9675-9682
Published online Aug 28, 2015. doi: 10.3748/wjg.v21.i32.9675
Published online Aug 28, 2015. doi: 10.3748/wjg.v21.i32.9675
Granulomatous reaction in hepatic inflammatory angiomyolipoma after chemoembolization and spontaneous rupture
Keita Kai, Department of Pathology, Saga University Hospital, Saga 849-8501, Japan
Atsushi Miyosh, Shinichi Aishima, Kota Wakiyama, Hirokazu Noshiro, Department of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan
Shinichi Aishima, Department of Pathology and Microbiology, Saga University Faculty of Medicine, Saga 849-8501, Japan
Shunya Nakashita, Shinji Iwane, Department of Internal Medicine, Saga University Faculty of Medicine, Saga 849-8501, Japan
Shinya Azama, Hiroyuki Irie, Department of Radiology, Saga University Faculty of Medicine, Saga 849-8501, Japan
Author contributions: Kai K is the main author of this article; Miyoshi A, Wakiyama K, Nakashita S, Iwane S and Azama S were attending doctors and performed clinical treatment and diagnosis including surgical operation; Aishima S, Irie H and Noshiro H reviewed the manuscript; all authors have read and approved the final manuscript.
Institutional review board statement: We consider that ethics approval is not needed because this is a single case report without personal information.
Informed consent statement: Written informed consent was obtained.
Conflict-of-interest statement: The authors declare that there are no conflicts of interest.
Open-Access: 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. See: http://creativecommons.org/licenses/by-nc/4.0/
Correspondence to: Keita Kai, MD, Department of Pathology, Saga University Hospital, Nabesima 5-1-1, Saga City, Saga 849-8501, Japan. kaikeit@cc.saga-u.ac.jp
Telephone: +81-952-343264 Fax: +81-952-342055
Received: February 20, 2015
Peer-review started: February 23, 2015
First decision: March 26, 2015
Revised: April 13, 2015
Accepted: June 9, 2015
Article in press: June 10, 2015
Published online: August 28, 2015
Processing time: 188 Days and 21.3 Hours
Peer-review started: February 23, 2015
First decision: March 26, 2015
Revised: April 13, 2015
Accepted: June 9, 2015
Article in press: June 10, 2015
Published online: August 28, 2015
Processing time: 188 Days and 21.3 Hours
Core Tip
Core tip: Hepatic angiomyolipoma (AML) is a rare benign neoplasm. Particularly, the inflammatory variant of hepatic AML is extremely rare. Spontaneous rupture of hepatic AML is also extremely rare phenomenon. The authors herein present a case of spontaneously ruptured hepatic inflammatory AML associated with extensive granulomatous reaction induced by chemoembolization. This case is not only rare, but also suggests that chemoembolization rarely causes granulomatous reaction in hepatic tissue.