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

Q2 Medicine
BMC Clinical Pathology Pub Date : 2015-09-03 eCollection Date: 2015-01-01 DOI:10.1186/s12907-015-0015-3
Takuto Nosaka, Katsushi Hiramatsu, Tomoyuki Nemoto, Yasushi Saito, Yoshihiko Ozaki, Kazuto Takahashi, Tatsushi Naito, Kazuya Ofuji, Hidetaka Matsuda, Masahiro Ohtani, Hiroyuki Suto, Yoshiaki Imamura, Yasunari Nakamoto
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引用次数: 6

Abstract

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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皮肤黑色素瘤治疗期间肝转移破裂:尸检病例报告。
背景:与原发性肝肿瘤相比,肝转移瘤的自发性破裂是罕见的。此外,vemurafenib是一种BRAF突变蛋白或基因产物的选择性抑制剂,据报道对携带BRAF V600E突变的转移性黑色素瘤患者非常有效。病例介绍:一名44岁女性曾接受手术切除右下肢恶性黑色素瘤。四年后,肝转移变得明显,并进行了经导管动脉栓塞(TAE)。然后她接受了vemurafenib治疗。肝转移灶的大小明显减小。两个月后,它们迅速扩大并破裂,需要紧急TAE。然而,患者发生失血性休克,并于术后第26天再次腹部出血死亡。结论:这是一例罕见的恶性黑色素瘤在vemurafenib治疗期间肝转移破裂的病例。尸检和免疫组织化学分析显示,转移性肿瘤中有丝裂原激活的蛋白激酶途径重新激活,提示对vemurafenib的继发性耐药可能是潜在的机制。
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来源期刊
BMC Clinical Pathology
BMC Clinical Pathology Medicine-Pathology and Forensic Medicine
CiteScore
3.30
自引率
0.00%
发文量
0
期刊介绍: BMC Clinical Pathology is an open access journal publishing original peer-reviewed research articles in all aspects of histopathology, haematology, clinical biochemistry, and medical microbiology (including virology, parasitology, and infection control). BMC Clinical Pathology (ISSN 1472-6890) is indexed/tracked/covered by PubMed, CAS, EMBASE, Scopus and Google Scholar.
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