血管内脂肪瘤伴血管外延伸,罕见现象及文献回顾

Mennatalla Hegazi , Charlene Yuan , Nii-Kabu Kabutey , Roy M Fujitani , Hari Keshava , Ali Mahtabifard , Anthony H Chau
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引用次数: 0

摘要

脂肪瘤是最常见的软组织肿瘤,占所有软组织肿块的一半。然而,血管内脂肪瘤(ivl)很少见。ivl已在各种主要静脉的病例报告中描述。它们通常是无症状的,是偶然发现的。考虑到恶性肿瘤的风险,脂肪肉瘤是成人中第二大常见的软组织肉瘤,占所有恶性肿瘤的1%,组织学分化很重要,手术切除仍然是文献中治疗的主要方法。我们提出的情况下,61岁的男性谁提出了左胸痛,辐射到他的左肩和手臂。在进一步的评估,病人承认左手肿胀和无力和增加突出静脉在左上肢。CT扫描示左侧无名静脉低密度肿块伴脂肪衰减,延伸至血管外并进入左侧颈内静脉,尺寸为2.3 × 2.0 × 5.2 cm。通过胸骨正中切口和左颈切口成功切除和重建无名静脉并再植左颈内静脉。术后过程平淡无奇,患者恢复良好。大口径血管内脂肪瘤的临床表现可能是微妙的和非特异性的。本病例报告的特点是这种罕见的血管肿瘤,包括当代文献回顾,总结诊断和治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intravascular lipoma with extravascular extension, a rare phenomena and review of the literature
Lipomas are the most common soft tissue tumors, accounting for half of all soft tissue masses. However, intravascular lipomas (IVLs) are rare. IVLs have been described in case reports in the various major veins. They are often asymptomatic and found incidentally. Given the risk of malignancy, as liposarcomas are the second most common soft tissue sarcoma in adults and account for 1 % of all malignancies, histological differentiation is important, and surgical excision remains the mainstay of treatment in the literature. We present the case of a 61-year-old male who presented with left chest pain that radiated to his left shoulder and arm. On further evaluation, the patient endorsed left-hand swelling and weakness and increased prominence of veins in the left upper extremity. He underwent a CT scan that showed a hypodense mass with fat attenuation in the left innominate vein extending extra-vascularly and into the left internal jugular vein, measuring 2.3 × 2.0 × 5.2 cm. Successful surgical excision and reconstruction of the innominate vein with reimplantation of the left internal jugular vein was performed through median sternotomy and left cervical incision. The postoperative course was unremarkable, and the patient recovered well. The clinical presentation of an intravascular lipoma in a large caliber vessel can be subtle and nonspecific. This case report characterizes this rare vascular tumor and includes a contemporary literature review, summarizing the diagnosis and treatment options.
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