Aortic Pleomorphic Sarcoma Presenting With Claudication: A Rare Diagnostic Challenge.

IF 0.7
Zehra Ünlü, Sedat Karaca, Aysen Yaprak Kapkin, Fatih Islamoglu
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Abstract

Aortic pleomorphic sarcomas are rare, aggressive vascular tumors often presenting with nonspecific symptoms that delay diagnosis. We describe a 53-year-old male who presented with isolated lower extremity claudication. Examination revealed absent pulses in the left leg, and duplex vascular ultrasound showed monophasic flow. CT angiography demonstrated a 48 mm infrarenal abdominal aortic aneurysm extending to the iliac bifurcation, a bulge in the left common iliac artery, and high-grade stenosis in a short segment. The patient underwent surgical repair with a Y-graft. Histopathological analysis confirmed undifferentiated pleomorphic sarcoma with a high Ki67 index (65%) and absence of specific immunohistochemical markers. Postoperative PET-CT revealed metastatic disease involving lungs, liver, and bones. The patient subsequently received systemic chemotherapy. This case highlights the diagnostic challenges of undifferentiated pleomorphic sarcoma when they present with isolated ischemic symptoms rather than signs of malignancy Early recognition through imaging and histopathology is essential, as surgical resection remains the cornerstone of treatment despite poor prognosis.

主动脉多形性肉瘤表现为跛行:罕见的诊断挑战。
主动脉多形性肉瘤是一种罕见的侵袭性血管肿瘤,通常表现为非特异性症状,延误诊断。我们描述了一个53岁的男性谁提出孤立的下肢跛行。检查发现左腿无脉搏,双血管超声显示单相血流。CT血管造影显示肾下腹主动脉瘤48 mm,延伸至髂分叉处,左侧髂总动脉隆起,短段高度狭窄。患者接受了移植y细胞的手术修复。组织病理学分析证实为未分化多形性肉瘤,Ki67指数高(65%),缺乏特异性免疫组织化学标志物。术后PET-CT显示转移性疾病累及肺、肝和骨。患者随后接受全身化疗。该病例强调了未分化多形性肉瘤的诊断挑战,当它们表现为孤立的缺血性症状而不是恶性肿瘤的体征时,通过影像学和组织病理学进行早期识别是必不可少的,因为尽管预后不良,手术切除仍然是治疗的基石。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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