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骶骨脊索瘤合并偶然发现的直肠腺癌:一例报告

Sacral chordoma with incidental rectal adenocarcinoma: a case report.

作者信息

Alshahri Jaffar, Alshehri Mohammed, Alnafesa Aminah, Widinly Mohammed, Alzaid Tariq, Alsulaimani Saleh, Abduljabbar Alaa

机构信息

King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

King Saud Medical City, Riyadh, Saudi Arabia.

出版信息

J Med Case Rep. 2021 Apr 12;15(1):195. doi: 10.1186/s13256-021-02728-2.

DOI:10.1186/s13256-021-02728-2
PMID:33845899
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8040199/
Abstract

BACKGROUND

We report a unique case of synchronous sacrococcygeal chordoma in association with rectal invasive adenocarcinoma. Retrorectal tumors are a rare disease caused by a variety of pathologies. To our knowledge, no prior cases of such a coincidental finding of both cancers have been reported in the literature.

CASE PRESENTATION

This is the case of a 74-year-old white middle eastern man, with known hypertension under treatment, who presented with complaints of progressive lower back pain associated with urinary incontinence over the past 12 months. Magnetic resonance imaging (MRI) of the pelvis showed a large midline, well-defined, oval-shaped lesion replacing the sacrococcygeal portion of the spine, with extension to the presacral region. Computed tomography (CT)-guided Tru-Cut biopsy revealed features suggestive of chordoma. At surgery, we performed excision of the entire mass en bloc, sacrectomy with rectus abdominis myocutaneous flap reconstruction and end sigmoid colostomy. Surgical histopathology proved it to be sacral dedifferentiated chordoma and rectal invasive adenocarcinoma. Overall, the patient recovered well postoperatively, was discharged home with functional stoma and on permanent Foley catheter use.

CONCLUSION

To the best of our knowledge, this is the only reported case of such a presentation, and sheds light on the approach and management. We hope that reporting such a case will add value to the medical literature.

摘要

背景

我们报告了一例罕见的同步性骶尾部脊索瘤合并直肠浸润性腺癌的病例。直肠后肿瘤是一种由多种病理情况引起的罕见疾病。据我们所知,此前文献中尚无关于这两种癌症同时出现的病例报道。

病例介绍

该病例为一名74岁的中东白人男性,正在接受高血压治疗,在过去12个月里出现进行性下背部疼痛并伴有尿失禁。骨盆磁共振成像(MRI)显示脊柱骶尾部有一个大的中线、边界清晰的椭圆形病变,延伸至骶前区域。计算机断层扫描(CT)引导下的Tru-Cut活检显示有脊索瘤的特征。手术中,我们整块切除了整个肿物,进行了骶骨切除术,并采用腹直肌肌皮瓣重建和乙状结肠末端造口术。手术组织病理学证实为骶骨去分化脊索瘤和直肠浸润性腺癌。总体而言,患者术后恢复良好,带功能性造口出院,需长期使用弗利导尿管。

结论

据我们所知,这是唯一报道的此类病例,为治疗方法和管理提供了参考。我们希望报告这样一个病例能为医学文献增添价值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/c87ef1cc1e0e/13256_2021_2728_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/bb76f87b33be/13256_2021_2728_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/02223f94328a/13256_2021_2728_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/4f902e2f9527/13256_2021_2728_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/c87ef1cc1e0e/13256_2021_2728_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/bb76f87b33be/13256_2021_2728_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/02223f94328a/13256_2021_2728_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/4f902e2f9527/13256_2021_2728_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e0d/8040199/c87ef1cc1e0e/13256_2021_2728_Fig4_HTML.jpg

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