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原发性脐尿管鳞状细胞癌:一例报告

Primary Urachal Squamous Cell Carcinoma: A Case Report.

作者信息

Rajyakodi Keerthana, Gunabooshanam Barathi, Paramasivan Sivakami Muthu Subramanian, Sundaram Sandhya

机构信息

Pathology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.

出版信息

Cureus. 2024 Oct 1;16(10):e70604. doi: 10.7759/cureus.70604. eCollection 2024 Oct.

Abstract

The urachus is a tubular vestigial remnant extending from the anterior dome of the bladder to the umbilicus. Carcinoma arising from it is uncommon but aggressive. Primary urachal carcinoma, an epithelial neoplasm, is one such abnormality which is rare and aggressive accounting for a very small portion of all bladder cancers. We herein present a case of a 48-year-old woman admitted with complaints of abdominal pain and abdominal mass. The mass was fixed to the anterior abdominal wall. A radiological investigation revealed a mass involving the midline of the anterior abdominal wall in the infraumbilical region with irregular margins along the course of the urachal ligament with surrounding fat stranding, suggesting a possibility of urachal malignancy with local extension. An ultrasound-guided core needle biopsy showed squamous cell carcinoma. The tumor was removed surgically. Further histological examination showed primary moderately differentiated squamous cell carcinoma of the urachus with metastasis to regional lymph nodes, extending into anterior abdominal muscles and up to the mucosa of the ileum. These findings correspond to the stage IVA of the Sheldon staging system for urachal carcinoma. Due to the rarity of urachal squamous cell carcinoma and limited research, definitive treatment guidelines are lacking. Current recommendations are based on small case series and lack a standardized staging system. Surgical intervention remains the cornerstone of treatment, often encompassing complete resection of the urachus, umbilicus, adjacent involved tissue with free margins, and potentially the bladder or regional lymph nodes to mitigate the risk of metastasis and local recurrence.

摘要

脐尿管是一条从膀胱前穹窿延伸至脐部的管状退化遗迹。起源于脐尿管的癌并不常见,但侵袭性强。原发性脐尿管癌是一种上皮性肿瘤,是一种罕见且侵袭性强的异常情况,在所有膀胱癌中所占比例极小。我们在此报告一例48岁女性患者,因腹痛和腹部肿块入院。肿块与前腹壁固定。影像学检查显示,在脐下区域前腹壁中线处有一肿块,沿脐尿管韧带走行边缘不规则,周围有脂肪条索状影,提示脐尿管恶性肿瘤伴局部浸润的可能性。超声引导下的粗针活检显示为鳞状细胞癌。肿瘤通过手术切除。进一步的组织学检查显示为原发性中度分化的脐尿管鳞状细胞癌,伴有区域淋巴结转移,侵犯至前腹壁肌肉直至回肠黏膜。这些发现符合Sheldon脐尿管癌分期系统的IVA期。由于脐尿管鳞状细胞癌罕见且研究有限,缺乏明确的治疗指南。目前的建议基于小病例系列,且缺乏标准化的分期系统。手术干预仍然是治疗的基石,通常包括完整切除脐尿管、脐部、切缘阴性的相邻受累组织,可能还包括膀胱或区域淋巴结,以降低转移和局部复发的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/79a6/11525946/d159a049b01e/cureus-0016-00000070604-i01.jpg

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