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阑尾印戒细胞癌伴子宫种植的影像学特征:一例报告

Imaging features of appendiceal signet ring cell carcinoma with uterine implantation: A case report.

作者信息

Liu Jia-Mi, Li Zhi, Qi Ling-Hong, Chu Bo-Liang, Deng Zai-Xing, Tang Feng-Yun

机构信息

Department of Radiology, Huzhou Maternity & Child Health Care Hospital, Huzhou 313000, Zhejiang Province, China.

Department of Gynaecology, Huzhou Maternity & Child Health Care Hospital, Huzhou 313002, Zhejiang Province, China.

出版信息

World J Radiol. 2025 Aug 28;17(8):110868. doi: 10.4329/wjr.v17.i8.110868.

Abstract

BACKGROUND

Signet ring cell carcinoma originating from the appendix is extremely rare, and the lack of specific clinical symptoms and imaging features makes preoperative diagnosis particularly challenging.

CASE SUMMARY

We report a case of a 49-year-old woman who presented with irregular vaginal bleeding lasting more than five months. Computed tomography (CT) and magnetic resonance imaging (MRI) revealed an enlarged appendix with a thickened wall and progressive enhancement after contrast administration. The uterine myometrium and cervix were markedly thickened, with heterogeneous density and signal intensity, along with progressive enhancement. The uterine serosal surface remained intact. Preoperative MRI suggested diffuse uterine adenomyosis; however, postoperative histopathology confirmed Signet ring cell carcinoma originating from the appendix with implantation involving the entire uterus.

CONCLUSION

Imaging showed appendiceal wall thickening and marked thickening of the uterine myometrium, with lesions demonstrating progressive enhancement after contrast administration. These findings should raise suspicion for the implantation of Signet ring cell carcinoma originating from the appendix and involving the uterus. Signet ring cell carcinoma originating from the appendix is relatively rare, and its imaging features are seldom reported, making preoperative diagnosis extremely challenging. This study retrospectively analyzes a case of Signet ring cell carcinoma originating from the appendix with implantation involving the entire uterus. The imaging characteristics of the appendix and the uterus were evaluated using CT and MRI to enhance awareness of this disease.

摘要

背景

起源于阑尾的印戒细胞癌极为罕见,缺乏特异性临床症状和影像学特征使得术前诊断极具挑战性。

病例摘要

我们报告一例49岁女性,出现持续5个多月的不规则阴道出血。计算机断层扫描(CT)和磁共振成像(MRI)显示阑尾增大,壁增厚,增强扫描后呈渐进性强化。子宫肌层和宫颈明显增厚,密度和信号强度不均匀,且呈渐进性强化。子宫浆膜面保持完整。术前MRI提示弥漫性子宫腺肌病;然而,术后组织病理学证实为起源于阑尾的印戒细胞癌伴子宫全层种植。

结论

影像学表现为阑尾壁增厚及子宫肌层明显增厚,病变在增强扫描后呈渐进性强化。这些表现应引起对起源于阑尾并累及子宫的印戒细胞癌种植的怀疑。起源于阑尾的印戒细胞癌相对罕见,其影像学特征鲜有报道,术前诊断极具挑战性。本研究回顾性分析一例起源于阑尾并累及子宫全层种植的印戒细胞癌病例。利用CT和MRI评估阑尾和子宫的影像学特征,以提高对该疾病的认识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/64e5/12400298/f2cc8c389ffe/wjr-17-8-110868-g001.jpg

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