Peritoneal Carcinomatosis with Gray-to-Black-Colored Peritoneum and Intestines Treated with Nivolumab: A Case Report.

IF 0.7 Q4 ONCOLOGY
Case Reports in Oncology Pub Date : 2025-07-28 eCollection Date: 2025-01-01 DOI:10.1159/000547654
Yuki Muroyama, Yuya Yoshida, Shiori Ishikawa, Fumiyoshi Fujishima, Takashi Suzuki
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Abstract

Introduction: Peritoneal carcinomatosis of unknown primary is a life-threatening condition that presents diagnostic and therapeutic challenges with poor prognosis. In 2021, nivolumab was approved for carcinoma of unknown primary in Japan.

Case presentation: A 70-year-old male underwent first-line nivolumab treatment for peritoneal carcinomatosis of unknown primary, in accordance with the patient's wishes. Four months after initiating treatment, he developed immune-related adverse event (irAE) hepatitis, which responded to methylprednisolone; however, the patient died a few days later. Autopsy revealed an uncommon presentation of thick, firm, gray peritoneum with globally gray-to-black ischemic intestines, massive adhesions, ascites, and disseminated peritoneal nodules. No evidence of superior mesenteric artery occlusion, segmental necrosis, or typical features of ischemic colitis or nonocclusive mesenteric ischemia was evident. Histological findings revealed fibrous thickening of the peritoneum. Pathological examination collectively suggested that the primary site of the peritoneal carcinomatosis was the non-mucinous adenocarcinoma, not otherwise specified, and mucinous adenocarcinoma of the appendix, which had not been detected on imaging or endoscopy. The final staging was pT4b, pN1a, pM1c, pStage IVC based on the TNM Classification (8th edition).

Conclusion: Although irAE colitis is well documented, peritoneal complications associated with immune checkpoint blockades have been scarcely reported in the literature, especially gray-colored peritoneum as in this case. The etiology is still unclear, but might collectively involve inflammation, stromal fibrosis, microscopic tumor invasion, and metabolic dysregulation in the tissue/tumor microenvironment. The unusual peritoneal presentation warrants further case accumulation and investigation into its pathogenesis to improve clinical management strategies.

尼武单抗治疗腹膜和肠灰黑色腹膜癌1例
原发不明的腹膜癌是一种危及生命的疾病,其诊断和治疗具有挑战性,预后不良。2021年,nivolumab在日本被批准用于治疗原发不明的癌症。病例介绍:一名70岁男性,根据患者的意愿,接受了未知原发腹膜癌的一线纳伏单抗治疗。开始治疗4个月后,他出现了免疫相关不良事件(irAE)肝炎,甲基强的松龙对其有反应;然而,几天后病人就去世了。尸检显示罕见的厚、硬、灰色腹膜,整体呈灰黑色缺血性肠,大量粘连,腹水和弥散性腹膜结节。没有证据表明肠系膜上动脉闭塞,节段性坏死,或缺血性结肠炎或非闭塞性肠系膜缺血的典型特征。组织学显示腹膜纤维增厚。病理检查共同提示腹膜癌的原发部位为未明确的非粘液腺癌和阑尾粘液腺癌,未在影像学和内镜检查中发现。根据TNM分类(第8版),最终分期为pT4b、pN1a、pM1c、pStage IVC。结论:尽管irAE型结肠炎有很好的文献记载,但与免疫检查点阻塞相关的腹膜并发症在文献中几乎没有报道,尤其是像本病例那样的灰色腹膜。病因尚不清楚,但可能涉及炎症、间质纤维化、显微肿瘤侵袭和组织/肿瘤微环境中的代谢失调。不寻常的腹膜表现需要进一步的病例积累和研究其发病机制,以改善临床治疗策略。
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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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
151
审稿时长
7 weeks
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