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尾肠囊肿的诊断挑战:一例隐匿性肛周肿物的病例报告

Diagnostic challenges of tailgut cysts: a case report on an occult perianal mass.

作者信息

Khalid Faraz, Naveed Haris, Ali Masab, Ansari Muhammad Saad, Shafiq Muhammad Sajjad, Ahmad Muhammad Husnain

机构信息

Department of Surgery, Punjab Medical College, Faisalabad, Punjab, Pakistan.

Department of Medicine, Tentishev Satkynbai Memorial Asian Medical Institute, Gagarina, Kant, Kyrgyzstan.

出版信息

Ann Med Surg (Lond). 2025 Jan 9;87(1):421-424. doi: 10.1097/MS9.0000000000002880. eCollection 2025 Jan.

DOI:10.1097/MS9.0000000000002880
PMID:40109612
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11918611/
Abstract

INTRODUCTION

Tailgut cysts, or retro-rectal cystic hamartomas, are rare congenital lesions arising from embryonic hindgut remnants, typically located in the retro-rectal area. These cysts present some diagnostic challenges due to vague symptoms and potential for malignancy.

CASE PRESENTATION

A 25-year-old female presented with a 5-year history of perianal swelling. MRI revealed a T2 hyperintense, multiseptated cystic lesion suggestive of a tailgut cyst. The cyst was surgically excised via a trans-sacral approach, and the specimen was sent for histopathological analysis.

CLINICAL DISCUSSION

The MRI findings were confirmed by histopathology, identifying a benign tailgut cyst. The patient had an uneventful recovery and was symptom-free at the 2-month follow-up.

CONCLUSION

Tailgut cysts can mimic other perianal masses, complicating diagnosis. Accurate diagnosis and successful treatment rely on clinical vigilance, advanced imaging, and histopathological confirmation. Early surgical resection is crucial to prevent complications, including malignancy.

摘要

引言

尾肠囊肿,即直肠后囊性错构瘤,是一种罕见的先天性病变,由胚胎后肠残余组织形成,通常位于直肠后区域。由于症状不明确以及存在恶变可能,这些囊肿带来了一些诊断挑战。

病例介绍

一名25岁女性有5年肛周肿胀病史。磁共振成像(MRI)显示一个T2高信号、多分隔的囊性病变,提示为尾肠囊肿。通过经骶骨入路手术切除该囊肿,并将标本送去做组织病理学分析。

临床讨论

组织病理学证实了MRI检查结果,确定为良性尾肠囊肿。患者恢复顺利,在2个月的随访中无症状。

结论

尾肠囊肿可类似其他肛周肿物,使诊断复杂化。准确诊断和成功治疗依赖于临床警惕性、先进的影像学检查以及组织病理学确认。早期手术切除对于预防包括恶变在内的并发症至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/c8bedb6eb118/ms9-87-421-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/2ecbb07e8194/ms9-87-421-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/6d7ce5d6ba16/ms9-87-421-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/c8bedb6eb118/ms9-87-421-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/2ecbb07e8194/ms9-87-421-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/6d7ce5d6ba16/ms9-87-421-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81e1/11918611/c8bedb6eb118/ms9-87-421-g003.jpg

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本文引用的文献

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Laparoscopic Resection Combined with a Transsacral Approach for a Recurrent Tailgut Cyst with a Refractory Fistula.腹腔镜切除联合经骶骨入路治疗难治性瘘管的复发性尾肠囊肿。
Acta Med Okayama. 2024 Apr;78(2):193-196. doi: 10.18926/AMO/66928.
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The SCARE 2023 guideline: updating consensus Surgical CAse REport (SCARE) guidelines.SCARE 2023 指南:更新共识外科病例报告(SCARE)指南。
Int J Surg. 2023 May 1;109(5):1136-1140. doi: 10.1097/JS9.0000000000000373.
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Malignant transformation of tailgut cyst to squamous cell carcinoma, a rare case with poor outcome.
尾肠囊肿恶变为鳞状细胞癌,罕见病例,预后不良。
Clin Case Rep. 2023 Feb 5;11(2):e6893. doi: 10.1002/ccr3.6893. eCollection 2023 Feb.
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Single-center Experience of 24 Cases of Tailgut Cyst.24例尾肠囊肿的单中心经验
Ann Coloproctol. 2019 Oct;35(5):268-274. doi: 10.3393/ac.2018.12.18. Epub 2019 Oct 31.
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Tailgut cyst: report of three cases and review of the literature.尾肠囊肿:三例报告并文献复习
Acta Chir Belg. 2019 Apr;119(2):110-117. doi: 10.1080/00015458.2017.1353758. Epub 2019 Feb 18.
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Benign tailgut cyst masquerading as a hemorrhoid.伪装成痔疮的良性尾肠囊肿。
Can J Gastroenterol Hepatol. 2014 Apr;28(4):183. doi: 10.1155/2014/757965.
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Tailgut cyst: MRI evaluation.尾肠囊肿:磁共振成像评估
AJR Am J Roentgenol. 2005 May;184(5):1519-23. doi: 10.2214/ajr.184.5.01841519.
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Tailgut cysts. Report of 53 cases.尾肠囊肿。53例报告。
Am J Clin Pathol. 1988 Feb;89(2):139-47. doi: 10.1093/ajcp/89.2.139.