Suppr超能文献

血管外科病房中下肢的对称性疼痛性溃疡:一项诊断挑战。与IgG-κ副蛋白血症相关的坏疽性脓皮病。

Symmetrical, painful ulceration of the lower limbs in a vascular surgery ward: a diagnostic challenge. Pyoderma gangrenosum associated with IgG-kappa paraproteinaemia.

作者信息

Simsek S, van den Haak R F F, Voskuyl A E, Rauwerda J A, Strack van Schijndel R J M

机构信息

Department of Endocrinology/Diabetes Centre, VU University Medical Center, PO Box 7057, 1007 MB Amsterdam, The Netherlands.

出版信息

Neth J Med. 2004 May;62(5):168-71.

Abstract

We describe a 61-year-old patient who had been suffering from chronic ulcers of both legs for 18 months. Initially, his condition was diagnosed as ischaemic because of an ankle-brachial index of 0.6, as confirmed by additional angiography. A successful femoro-infragenual bypass procedure was performed, but the ulcers increased in size and number. He was then extensively analysed for a possible (macro)vascular origin of his symptoms. Angiographic analysis of both legs showed no arterial stenosis or occlusion. Despite the extensive experience of the vascular surgeons with leg ulcers, consultations by internal medicine, vascular medicine and dermatology, and tissue examination by our pathologists, pyoderma gangrenosum was not recognised. During a multidisciplinary meeting one of the specialists, to whom the lesions were shown, immediately considered the diagnosis on clinical grounds. The additional finding of IgG-kappa paraproteinaemia and improvement of the ulcers on treatment with corticosteroids were consistent with the diagnosis. Although the majority of patients on the vascular surgery ward have ulcers caused by ischaemia or a combined arterial/venous origin, another (rare) cause, namely pyoderma gangrenosum in association with IgG-kappa paraproteinaemia without the presence of multiple myeloma, should be taken into account.

摘要

我们描述了一位61岁的患者,他双腿慢性溃疡已有18个月。最初,由于踝肱指数为0.6,经额外血管造影证实,其病情被诊断为缺血性。成功进行了股-膝下旁路手术,但溃疡的大小和数量却增加了。随后,对其症状可能的(大)血管起源进行了全面分析。双腿的血管造影分析未显示动脉狭窄或闭塞。尽管血管外科医生在治疗腿部溃疡方面经验丰富,内科、血管医学和皮肤科也进行了会诊,且我们的病理学家进行了组织检查,但坏疽性脓皮病仍未被识别。在一次多学科会议上,一位看过病变的专家根据临床情况立即做出了诊断。IgG-κ副蛋白血症的额外发现以及使用皮质类固醇治疗后溃疡的改善与诊断相符。尽管血管外科病房的大多数患者的溃疡是由缺血或动静脉联合起源引起的,但另一种(罕见)病因,即与IgG-κ副蛋白血症相关的坏疽性脓皮病(无多发性骨髓瘤)也应予以考虑。

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