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Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report

BACKGROUND: The spontaneous rupture of hepatic metastases is rare compared to that of primary hepatic tumors. In addition, vemurafenib, a selective inhibitor of the mutant BRAF protein or gene product, has been reported to be extremely effective in patients with metastatic melanoma who harbor a BRAF...

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Autores principales: Nosaka, Takuto, Hiramatsu, Katsushi, Nemoto, Tomoyuki, Saito, Yasushi, Ozaki, Yoshihiko, Takahashi, Kazuto, Naito, Tatsushi, Ofuji, Kazuya, Matsuda, Hidetaka, Ohtani, Masahiro, Suto, Hiroyuki, Imamura, Yoshiaki, Nakamoto, Yasunari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559873/
https://www.ncbi.nlm.nih.gov/pubmed/26346246
http://dx.doi.org/10.1186/s12907-015-0015-3
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author Nosaka, Takuto
Hiramatsu, Katsushi
Nemoto, Tomoyuki
Saito, Yasushi
Ozaki, Yoshihiko
Takahashi, Kazuto
Naito, Tatsushi
Ofuji, Kazuya
Matsuda, Hidetaka
Ohtani, Masahiro
Suto, Hiroyuki
Imamura, Yoshiaki
Nakamoto, Yasunari
author_facet Nosaka, Takuto
Hiramatsu, Katsushi
Nemoto, Tomoyuki
Saito, Yasushi
Ozaki, Yoshihiko
Takahashi, Kazuto
Naito, Tatsushi
Ofuji, Kazuya
Matsuda, Hidetaka
Ohtani, Masahiro
Suto, Hiroyuki
Imamura, Yoshiaki
Nakamoto, Yasunari
author_sort Nosaka, Takuto
collection PubMed
description BACKGROUND: The spontaneous rupture of hepatic metastases is rare compared to that of primary hepatic tumors. In addition, vemurafenib, a selective inhibitor of the mutant BRAF protein or gene product, has been reported to be extremely effective in patients with metastatic melanoma who harbor a BRAF V600E mutation. CASE PRESENTATION: A 44-year-old female had previously undergone surgery for resection of a malignant melanoma in the lower right leg. Four years later, hepatic metastases became apparent, and transcatheter arterial embolization (TAE) was performed. Then she underwent treatment with vemurafenib. The size of the hepatic metastases markedly decreased. Two months later, they enlarged rapidly and ruptured, requiring emergency TAE. However, the patient developed hemorrhagic shock and died of renewed intra-abdominal bleeding on the 26th postoperative day. CONCLUSIONS: This is a rare case of ruptured hepatic metastases of malignant melanoma during treatment with vemurafenib. Postmortem examination and immunohistochemical analysis indicated reactivation of the mitogen-activated protein kinase pathway in the metastatic tumor, suggesting secondary resistance to vemurafenib as the possible underlying mechanism.
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spelling pubmed-45598732015-09-05 Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report Nosaka, Takuto Hiramatsu, Katsushi Nemoto, Tomoyuki Saito, Yasushi Ozaki, Yoshihiko Takahashi, Kazuto Naito, Tatsushi Ofuji, Kazuya Matsuda, Hidetaka Ohtani, Masahiro Suto, Hiroyuki Imamura, Yoshiaki Nakamoto, Yasunari BMC Clin Pathol Case Report BACKGROUND: The spontaneous rupture of hepatic metastases is rare compared to that of primary hepatic tumors. In addition, vemurafenib, a selective inhibitor of the mutant BRAF protein or gene product, has been reported to be extremely effective in patients with metastatic melanoma who harbor a BRAF V600E mutation. CASE PRESENTATION: A 44-year-old female had previously undergone surgery for resection of a malignant melanoma in the lower right leg. Four years later, hepatic metastases became apparent, and transcatheter arterial embolization (TAE) was performed. Then she underwent treatment with vemurafenib. The size of the hepatic metastases markedly decreased. Two months later, they enlarged rapidly and ruptured, requiring emergency TAE. However, the patient developed hemorrhagic shock and died of renewed intra-abdominal bleeding on the 26th postoperative day. CONCLUSIONS: This is a rare case of ruptured hepatic metastases of malignant melanoma during treatment with vemurafenib. Postmortem examination and immunohistochemical analysis indicated reactivation of the mitogen-activated protein kinase pathway in the metastatic tumor, suggesting secondary resistance to vemurafenib as the possible underlying mechanism. BioMed Central 2015-09-03 /pmc/articles/PMC4559873/ /pubmed/26346246 http://dx.doi.org/10.1186/s12907-015-0015-3 Text en © Nosaka et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Nosaka, Takuto
Hiramatsu, Katsushi
Nemoto, Tomoyuki
Saito, Yasushi
Ozaki, Yoshihiko
Takahashi, Kazuto
Naito, Tatsushi
Ofuji, Kazuya
Matsuda, Hidetaka
Ohtani, Masahiro
Suto, Hiroyuki
Imamura, Yoshiaki
Nakamoto, Yasunari
Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
title Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
title_full Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
title_fullStr Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
title_full_unstemmed Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
title_short Ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
title_sort ruptured hepatic metastases of cutaneous melanoma during treatment with vemurafenib: an autopsy case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4559873/
https://www.ncbi.nlm.nih.gov/pubmed/26346246
http://dx.doi.org/10.1186/s12907-015-0015-3
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