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同一病变中结直肠癌与免疫球蛋白G4相关疾病并存:一例罕见的分子分类病例

Coexistence of Colorectal Cancer and Immunoglobulin G4-Related Disease in the Same Lesion: A Rare Case with Molecular Classification.

作者信息

Na Kiyong, Kim So-Woon

机构信息

Department of Pathology, Kyung Hee University Hospital, Kyung Hee University College of Medicine, Seoul 05278, Republic of Korea.

出版信息

Diagnostics (Basel). 2024 Jan 8;14(2):138. doi: 10.3390/diagnostics14020138.

Abstract

Immunoglobulin G4-related disease (IgG4-RD) is a novel fibroinflammatory disorder characterized by enlargement of the involved organs, elevated IgG4 levels, and abundant infiltration of IgG4-positive plasma cells. Indeed, primary colon cancers arising from IgG4-RD are rare. This case report describes a rare occurrence of simultaneous colorectal cancer and IgG4-RD in the same lesion in a 62-year-old male patient. The patient underwent a right hemicolectomy under the suspicion of primary colon cancer. The mass was grossly well-defined and yellowish tan, and the background colon was fibrotic. Microscopically, the tumor cells showed glandular differentiation characteristic of adenocarcinoma in a background of dense lymphoplasmacytic infiltration with fibrosis and obliterative phlebitis in the pericolic fat tissue. IgG4 immunohistochemical staining showed diffuse positivity in infiltrating plasma cells. The patient was administered adjuvant chemotherapy and prednisolone therapy. The patient's serum IgG4 levels gradually decreased, and a follow-up positron emission tomography-computed tomography scan 1 year after surgery showed no evidence of local or distant recurrence of colorectal cancer. IgG4-RD occurring concurrently with primary colon adenocarcinoma has not been reported. Increased awareness of this rare coexistence can guide clinicians in navigating diagnostic complexities and selecting optimal therapeutic strategies.

摘要

免疫球蛋白G4相关疾病(IgG4-RD)是一种新型的纤维炎症性疾病,其特征为受累器官肿大、IgG4水平升高以及IgG4阳性浆细胞大量浸润。事实上,由IgG4-RD引发的原发性结肠癌很罕见。本病例报告描述了一名62岁男性患者在同一病变部位同时发生结直肠癌和IgG4-RD这一罕见情况。该患者因疑似原发性结肠癌接受了右半结肠切除术。肿块肉眼观边界清晰,呈黄棕色,背景结肠纤维化。显微镜下,肿瘤细胞在密集淋巴细胞浆细胞浸润背景下呈腺癌特征性的腺管分化,结肠周围脂肪组织有纤维化和闭塞性静脉炎。IgG4免疫组化染色显示浸润浆细胞弥漫阳性。患者接受了辅助化疗和泼尼松龙治疗。患者血清IgG4水平逐渐下降,术后1年的随访正电子发射断层扫描-计算机断层扫描显示无结直肠癌局部或远处复发迹象。原发性结肠腺癌并发IgG4-RD尚未见报道。提高对这种罕见共存情况的认识可指导临床医生应对诊断复杂性并选择最佳治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/798c/10814229/15003145963f/diagnostics-14-00138-g001.jpg

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