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直肠印戒细胞癌转移至同期肾细胞癌:一例报告

Signet ring cell carcinoma of rectum metastasizing to synchronous renal cell carcinoma: a case report.

作者信息

Krsteska Blagica, Jovanovic Rubens, Eftimov Aleksandar, Ilievski Boro, Hadzi-Mancev Dragan, Osmani Bujar, Kostadinova-Kunovska Slavica

机构信息

Institute of Pathology, Faculty of Medicine, Ss. Cyril and Methodius University in Skopje, Skopje, North Macedonia.

Faculty of Medicine, , University Clinic of Abdominal Surgery-Ss. Cyril and Methodius University in Skopje , Skopje, North Macedonia.

出版信息

J Med Case Rep. 2021 Mar 18;15(1):123. doi: 10.1186/s13256-021-02749-x.

Abstract

BACKGROUND

Rectal signet ring cell carcinoma is a rare type of colorectal adenocarcinoma characterized by an aggressive biological behavior and poor prognosis. The co-occurrence of colorectal carcinoma and renal cell carcinoma (RCC) has found in many hundreds of patients, many of whom also have additional malignancies. Cancer to cancer metastasis is rare and an uncommon phenomenon in malignancy, especially at the time of initial diagnosis, suggesting a genetic susceptibility.

CASE PRESENTATION

We present the case of a 66-year-old Macedonian man with synchronous rectal signet ring cell carcinoma and RCC with tumor to tumor metastasis feature. He underwent a left nephrectomy and anterior rectal resection after complaining of constipation for 3-4 months and the appearance of synchronous tumors on the imaging studies. Morphology and immunohistochemical analysis of specimens from the RCC revealed signet ring cells identical to the rectal signet ring cell carcinoma. The next-generation sequencing study revealed mutations in TP53 and ERBB2, and microsatellite stable signet ring cell carcinoma was determined by deoxyribonucleic acid (DNA) sequencing.

CONCLUSIONS

Cancer to cancer metastasis, although rare, needs to be considered in synchronous tumors. RCC, when diagnosed in multiple synchronous tumors, should be examined carefully. The paucity of reported cases indicates the need for advanced research in imaging methods for metastasis and new therapeutic approaches.

摘要

背景

直肠印戒细胞癌是一种罕见的结直肠腺癌,具有侵袭性生物学行为和较差的预后。在数百名患者中发现了结直肠癌和肾细胞癌(RCC)同时存在的情况,其中许多患者还患有其他恶性肿瘤。癌至癌转移罕见,在恶性肿瘤中是一种不常见的现象,尤其是在初始诊断时,提示存在遗传易感性。

病例介绍

我们报告了一例66岁的马其顿男性患者,患有同步性直肠印戒细胞癌和RCC,具有肿瘤至肿瘤转移特征。他在抱怨便秘3 - 4个月且影像学检查发现同步性肿瘤后,接受了左肾切除术和直肠前切除术。对RCC标本的形态学和免疫组织化学分析显示,其印戒细胞与直肠印戒细胞癌相同。下一代测序研究揭示了TP53和ERBB2基因的突变,并通过脱氧核糖核酸(DNA)测序确定为微卫星稳定的印戒细胞癌。

结论

癌至癌转移虽然罕见,但在同步性肿瘤中需要考虑。当在多个同步性肿瘤中诊断出RCC时,应仔细检查。报告病例的稀少表明需要对转移的成像方法和新的治疗方法进行深入研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d2aa/7972208/0f6236fca2a8/13256_2021_2749_Fig1_HTML.jpg

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