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手部罕见的“组织细胞血管瘤”病例。

A rare case of 'histiocytoid haemangioma' of the hand.

机构信息

Department of Plastic Surgery, University of Naples "Federico II", Via Pansini 5, 80122 Naples, Italy.

出版信息

J Plast Reconstr Aesthet Surg. 2013 Nov;66(11):e318-20. doi: 10.1016/j.bjps.2013.04.027. Epub 2013 May 11.

Abstract

Histiocytoid haemangioma has been identified by Rosai in 1979 as a group of vascular tumour-like lesions. This lesion can occur in a wide variety of sites. Surgical excision is the treatment of choice. We present the case of a 35-year-old man with a swelling in the thenar region of his right hand. Preoperative X-rays, magnetic resonance imaging (MRI) and angio-computed tomography (angio-CT) demonstrated a lesion invading the radial digital artery to the index finger without any bone erosion. It was excised 'en bloc' with the artery itself. The radial digital nerve to the index finger and the main digital artery to the thumb were preserved. No local recurrence was observed at the 3-year follow-up. Histiocytoid haemangioma of the hand is a rare disease, and patients should undergo early surgical treatment to achieve complete excision of the lesion without any functional deficit.

摘要

组织细胞样血管瘤于 1979 年由 Rosai 确定为一组类似于血管肿瘤的病变。这种病变可发生在多种部位。手术切除是首选治疗方法。我们报告了一名 35 岁男性右手大鱼际区肿胀的病例。术前 X 线、磁共振成像(MRI)和血管计算机断层扫描(angio-CT)显示病变侵犯了食指的桡侧指动脉,没有任何骨质侵蚀。它与动脉本身一起整块切除。食指的桡侧指神经和拇指的主要指动脉被保留。在 3 年的随访中未观察到局部复发。手部组织细胞样血管瘤是一种罕见疾病,患者应进行早期手术治疗,以实现完全切除病变,而不造成任何功能缺陷。

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