血管源性 Leiomyosarcoma:从误诊中汲取的教训

IF 0.7 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Egyptian Journal of Radiology and Nuclear Medicine Pub Date : 2024-08-26 DOI:10.1186/s43055-024-01336-6
Mohamed Salah Ayyad, Mahmoud Fawzy Elbellasy, Amany Hassan, Mona Gad
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引用次数: 0

摘要

血管源性雷米肉瘤(LMS)是一种罕见的软组织肉瘤。虽然它们大多来自腹膜后的主要血管结构,但有些病例也可能来自大腿上较小的血管结构,如股静脉。由于其来源于血管结构,可能会被误诊为深静脉血栓(DVT),因此给诊断带来了挑战。我们接诊了一例 45 岁女性患者,她患有左股静脉和髂静脉 LMS,血管超声(US)报告曾将其描述为累及股静脉和髂外静脉的广泛深静脉血栓。患者在接受处方抗凝药物治疗后病情未见好转。七个月后,患者接受了造影剂计算机断层扫描(CT)检查,发现左侧股总静脉和髂外静脉解剖部位有一个软组织肿块。患者接受了 US 引导下的真切活检和髂淋巴结切口活检,结果显示为亮肌肉瘤。患者在首次就诊时接受了盆腔和左大腿血管超声和磁共振成像检查。七个月后,她接受了腹部和盆腔对比增强 CT 检查。由于肿瘤无法手术,患者被转到肿瘤科接受适当的化疗方案。虽然血管源性子宫肌瘤是一种罕见的肿瘤,但通常被低估。高怀疑指数有助于临床医生怀疑此类肿瘤,为早期诊断和治疗节省时间。对于静脉血栓患者,在使用抗凝剂后病情未见好转的情况下应特别小心。当有怀疑时,计算机断层扫描和磁共振成像等其他方式有助于确诊。
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Leiomyosarcoma of vascular origin: lessons learned from misdiagnosis
Leiomyosarcoma (LMS) of vascular origin is a rare entity of soft tissue sarcomas. Although they arise mostly from retroperitoneal major vascular structures, some encountered cases may arise from the smaller vascular structures of the thigh as the femoral vein. Due to their origin from the vascular structures, they represent a diagnostic challenge as they may be misdiagnosed as deep vein thrombosis (DVT). We present a case of a 45-year-old woman with left femoral and iliac vein LMS that was previously described in the vascular ultrasound (US) report as extensive DVT involving the femoral and external iliac veins. The patient did not improve after receiving the prescribed anticoagulants. Seven months later, the patient underwent computerized tomography (CT) with contrast, revealing a soft tissue mass in the anatomical site of the left common femoral and external iliac veins. The patient underwent both US-guided tru-cut biopsy and incisional biopsy from the iliac lymph nodes which revealed leiomyosarcoma. The patient underwent both vascular ultrasound and magnetic resonance imaging of the pelvis and the left thigh at the time of the first presentation. Seven months later, she underwent contrast-enhanced CT of the abdomen and pelvis. The patient was referred to the oncology department to receive the appropriate chemotherapy protocol as the tumor was inoperable. Although leiomyosarcoma of vascular origin is a rare entity of neoplasms, it is usually underestimated. A high index of suspicion would help the clinician to suspect such a neoplasm and save time for early diagnosis and management. Special caution should be taken for patients with venous thrombosis not improving on anticoagulants. When there is suspicion, other modalities such as computerized tomography and magnetic resonance imaging help confirm the diagnosis.
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来源期刊
Egyptian Journal of Radiology and Nuclear Medicine
Egyptian Journal of Radiology and Nuclear Medicine Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
1.70
自引率
10.00%
发文量
233
审稿时长
27 weeks
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