Suppr超能文献

乙状结肠早期原发性平滑肌肉瘤的诊断与治疗:一例报告

Diagnostic and therapy of an early-stage primary leiomyosarcoma of the sigmoid colon: A case report.

作者信息

Fickenscher M, Gvozdenovic N, Ponsel O

机构信息

Department of General and Visceral Surgery Klinikum Bayreuth Bayreuth Germany.

出版信息

Clin Case Rep. 2024 Jul 12;12(7):e9178. doi: 10.1002/ccr3.9178. eCollection 2024 Jul.

Abstract

KEY CLINICAL MESSAGE

Primary leiomyosarcoma of the colon is a very rare tumor entity. Because of unspecific findings, diagnostic can be challenging. Most cases are diagnosed in advanced stages with poor overall survival. Unclear histological findings of smooth muscle cell tissue in colon biopsies together with a tumor of the colon wall in computed tomography (CT) imaging should lead to the differential diagnosis of primary colonic leiomyosarcoma and further diagnostic procedures.

ABSTRACT

Primary colonic leiomyosarcoma is an extremely rare tumor entity arising from smooth muscle cells in the colon wall. Only 0.1% of all colorectal malignancies are leiomyosarcomas. Most patients are diagnosed in advanced disease stages. The overall survival rates are low, and recurrence rates are high. Only few data regarding the outcome in localized early disease stages are available. We report the case of an early-stage primary leiomyosarcoma of the sigmoid colon treated with surgical resection. We present the case of a 53-year-old male patient who underwent a colonoscopy due to intermittent rectal bleeding. Colonoscopy revealed an intraluminal polypoid growing tumor in the sigmoid colon. A biopsy was performed with inconclusive histological results. A CT scan revealed a process in the sigmoid colon with wall thickening; there was no evidence of metastatic lesions. After laparoscopic oncological resection of the sigmoid colon, histological examination surprisingly revealed a localized high-grade leiomyosarcoma. Primary leiomyosarcoma of the colon is a rare tumor entity and diagnostic can be challenging. Only a few patients with colonic leiomyosarcoma diagnosed in localized early disease stages and treated with complete surgical resection have been reported in the literature. These patients seem to have a better prognosis with longer overall survival. Because of unspecific diagnostic findings and the lack of symptoms in early disease stages, interdisciplinary collaborations between gastroenterologists, radiologists, pathologists, and surgeons are crucial for early diagnosis and treatment.

摘要

关键临床信息

原发性结肠平滑肌肉瘤是一种非常罕见的肿瘤类型。由于临床表现不具特异性,诊断具有挑战性。大多数病例在晚期才被诊断出来,总体生存率较差。结肠活检中平滑肌细胞组织的组织学表现不明确,同时计算机断层扫描(CT)成像显示结肠壁有肿瘤,应考虑原发性结肠平滑肌肉瘤的鉴别诊断,并进行进一步的诊断程序。

摘要

原发性结肠平滑肌肉瘤是一种极其罕见的肿瘤类型,起源于结肠壁的平滑肌细胞。在所有结直肠恶性肿瘤中,平滑肌肉瘤仅占0.1%。大多数患者在疾病晚期被诊断出来。总体生存率较低,复发率较高。关于局限性早期疾病阶段的预后数据很少。我们报告了一例经手术切除治疗的乙状结肠早期原发性平滑肌肉瘤病例。我们介绍了一名53岁男性患者,因间歇性直肠出血接受结肠镜检查。结肠镜检查发现乙状结肠腔内有一个息肉样生长的肿瘤。进行了活检,但组织学结果不明确。CT扫描显示乙状结肠有病变,肠壁增厚;没有转移病变的证据。在对乙状结肠进行腹腔镜肿瘤切除术后,组织学检查令人惊讶地发现是局限性高级别平滑肌肉瘤。原发性结肠平滑肌肉瘤是一种罕见的肿瘤类型,诊断具有挑战性。文献中仅报道了少数在局限性早期疾病阶段被诊断出并接受完全手术切除治疗的结肠平滑肌肉瘤患者。这些患者似乎预后较好,总体生存期较长。由于诊断结果不具特异性且早期疾病阶段缺乏症状,胃肠病学家、放射科医生、病理学家和外科医生之间的跨学科合作对于早期诊断和治疗至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1555/11245400/629c3d429cde/CCR3-12-e9178-g003.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验