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原发性结肠绒毛膜癌:病例报告及文献综述

Primary Choriocarcinoma of Colon: Case Report and Literature Review.

作者信息

Okazaki Naoto, Tanaka Akira, Yasuda Masanori, Hiraoka Yu, Ishikawa Shintaro, Yoshizawa Masatoshi, Hayashi Hisashi, Gunji Yoshio, Hirano Yasumitsu

机构信息

Department of Gastroenterological Surgery, Saitama Medical University International Medical Center, Hidaka, Japan.

Department of Surgery, Koseikai Hospital, Kawagoe, Japan.

出版信息

J Anus Rectum Colon. 2025 Jul 25;9(3):356-361. doi: 10.23922/jarc.2024-114. eCollection 2025.

DOI:10.23922/jarc.2024-114
PMID:40740757
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12307013/
Abstract

Primary colorectal choriocarcinoma is extremely rare with only 35 cases described in the literature during over 40 years. The neoplasm is characterized by biphasic tumor growth composed of adenocarcinomatous and choriocarcinomatous differentiation. Diagnostic elusiveness, aggressive nature and lack of established treatment make the prognosis extremely poor, and most patients die during the first year after diagnosis. We present a 66-year-old man with a primary choriocarcinoma of the transverse colon presenting with peritoneal metastasis and acute colonic obstruction. The patient was treated with systemic three-drug chemotherapy (mFOLFOXIRI: 5-fluorouracil/leucovorin + oxaliplatin + irinotecan) in combination with bevacizumab, a highly active regimen for metastatic colorectal adenocarcinoma. Tumor shrinkage was accompanied by a decrease of mononucleated trophoblast-like carcinoma cells in an endoscopic biopsy during the treatment, and the symptoms of disease were relieved within a quite short period of therapy, though rapid regrowth associated with serum beta human chorionic gonadotropin escalation occurred following discontinuation of therapy. The patient died 8 months after the initial diagnosis. Although our patient survived longer than the median survival period documented in the literature, further cases will need to be examined in the future to establish whether this antitumor treatment is effective to prolong survival.

摘要

原发性结直肠癌极为罕见,40多年来文献中仅描述了35例。该肿瘤的特征是由腺癌和绒毛膜癌分化组成的双相肿瘤生长。诊断困难、侵袭性强且缺乏既定的治疗方法导致预后极差,大多数患者在诊断后的第一年内死亡。我们报告了一名66岁男性,患有横结肠原发性绒毛膜癌,伴有腹膜转移和急性结肠梗阻。该患者接受了全身性三药化疗(mFOLFOXIRI:5-氟尿嘧啶/亚叶酸钙+奥沙利铂+伊立替康)联合贝伐单抗治疗,这是一种用于转移性结直肠腺癌的高效方案。治疗期间,肿瘤缩小伴随着内镜活检中单核滋养层样癌细胞数量的减少,且在相当短的治疗期内疾病症状得到缓解,尽管治疗中断后肿瘤迅速复发并伴有血清β-人绒毛膜促性腺激素升高。患者在初次诊断后8个月死亡。虽然我们的患者存活时间长于文献记载的中位生存期,但未来还需要进一步研究更多病例,以确定这种抗肿瘤治疗是否能有效延长生存期。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/681126ca761d/2432-3853-9-3-0356-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/ba7db16adc38/2432-3853-9-3-0356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/70c8fe9c98d8/2432-3853-9-3-0356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/681126ca761d/2432-3853-9-3-0356-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/ba7db16adc38/2432-3853-9-3-0356-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/70c8fe9c98d8/2432-3853-9-3-0356-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b2/12307013/681126ca761d/2432-3853-9-3-0356-g003.jpg

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本文引用的文献

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Role of GATA3 in tumor diagnosis: A review.GATA3 在肿瘤诊断中的作用:综述。
Pathol Res Pract. 2021 Oct;226:153611. doi: 10.1016/j.prp.2021.153611. Epub 2021 Sep 13.
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Unusual abscess masquerading as poorly differentiated adenocarcinoma of the colon showing characteristics of choriocarcinoma.表现为绒毛膜癌特征的不寻常脓肿,伪装成结肠低分化腺癌。
Autops Case Rep. 2020 May 29;10(3):e2020145. doi: 10.4322/acr.2020.145.
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Primary colon adenocarcinoma with choriocarcinoma differentiation: a case report and review of the literature.
伴有绒毛膜癌分化的原发性结肠腺癌:1例报告并文献复习
J Med Case Rep. 2020 Nov 16;14(1):220. doi: 10.1186/s13256-020-02544-0.
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Gestational and Non-gestational Trophoblastic Disease. Guideline of the DGGG, OEGGG and SGGG (S2k Level, AWMF Registry No. 032/049, December 2015).妊娠性和非妊娠性滋养细胞疾病。德国妇产科学会、奥地利妇产科学会和瑞士妇产科学会指南(S2k级别,德国医学质量与效率理事会注册号032/049,2015年12月)
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World J Surg Oncol. 2013 Jan 28;11:23. doi: 10.1186/1477-7819-11-23.
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