Successful outcome achieved with adjuvant chemotherapy with irinotecan plus cisplatin in rectal neuroendocrine carcinoma: a case report

IF 0.7 Q4 SURGERY Surgical Case Reports Pub Date : 2024-09-19 DOI:10.1186/s40792-024-02010-9
Yoshitaka Saegusa, Shintaro Akabane, Manabu Shimomura, Hiroshi Okuda, Takuya Yano, Tetsuya Mochizuki, Wako Inoue, Mizuki Yamaguchi, Shinji Yamaguchi, Kazuhiro Sentani, Masami Yamauchi, Kentaro Tokumo, Hideki Ohdan
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Abstract

Rectal neuroendocrine carcinomas (NECs) are rare and associated with poorer prognoses compared to conventional adenocarcinomas. The efficacy of adjuvant chemotherapy for resectable rectal NECs remains uncertain. Herein, we present a case of rectal NEC successfully treated with postoperative chemotherapy using irinotecan plus cisplatin. A 48-year-old woman with a history of endometrial cancer presented with an intramural rectal tumour detected on follow-up imaging. Colonoscopy revealed a 30 mm submucosal tumour, and laparoscopic low anterior resection was performed. Histopathological examination showed poorly differentiated atypical cells with solid growth patterns. Metastasis from the uterine cancer was ruled out due to histological differences between the primary uterine tumour and the rectal lesion, as well as the absence of hormone receptor immunohistochemical expression. Further immunohistochemical analysis revealed diffuse CD56 positivity, a high mitotic rate (> 20/10 high power fields) and a Ki-67 labelling index exceeding 70%. Based on these findings, a diagnosis of rectal NEC, T3N0M0, Stage IIB (UICC 8th edition), was established. Given the aggressive nature of the tumour evidenced by a high Ki-67 labelling index, adjuvant chemotherapy comprising six cycles of irinotecan plus cisplatin was administered to mitigate the risk of recurrence. At the 3-year follow-up, the patient was free of disease recurrence. This case highlights the importance of multidisciplinary surgical interventions followed by adjuvant chemotherapy in managing rectal NECs.
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直肠神经内分泌癌辅助化疗伊立替康加顺铂取得成功:病例报告
直肠神经内分泌癌(NEC)十分罕见,与传统腺癌相比,其预后较差。对于可切除的直肠NEC,辅助化疗的疗效仍不确定。在此,我们介绍一例使用伊立替康加顺铂术后化疗成功治疗直肠NEC的病例。一位 48 岁的女性患者曾患子宫内膜癌,随访造影时发现直肠内肿瘤。结肠镜检查发现了一个 30 毫米的黏膜下肿瘤,于是进行了腹腔镜低位前切除术。组织病理学检查显示,肿瘤为分化不良的非典型细胞,呈实性生长。由于原发子宫肿瘤和直肠病变在组织学上存在差异,而且没有激素受体免疫组化表达,因此排除了子宫癌转移的可能性。进一步的免疫组化分析显示,CD56呈弥漫阳性,有丝分裂率高(> 20/10 高倍视野),Ki-67标记指数超过70%。根据这些结果,确诊为直肠 NEC,T3N0M0,IIB 期(UICC 第 8 版)。鉴于肿瘤的侵袭性(Ki-67标记指数较高),患者接受了伊立替康加顺铂的辅助化疗,共6个周期,以降低复发风险。在 3 年的随访中,患者没有再复发。本病例强调了多学科手术干预和辅助化疗在治疗直肠坏死性溃疡中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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审稿时长
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