Mitzy Placencia, Eugene Wong
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引用次数: 1

摘要

由于血栓性静脉炎并大量静脉阻塞而引起的肢体坏疽和静脉纤维化是一种罕见的疾病,常与原发性动脉闭塞性疾病相混淆。由于大量静脉闭塞和相关的动脉静脉痉挛,血流可能受阻至四肢,导致发绀并最终发生坏疽。认识到这一点是很重要的,因为这种坏疽通常是肤浅的或局限于手指。这类坏疽的保守治疗与原发性动脉功能不全坏疽的根治性治疗不同。这种疾病被称为“蓝灰色粘液病”、“格雷瓜尔蓝色静脉炎”、“四肢急性大面积静脉闭塞”、“假性栓塞性静脉炎”和“静脉源性坏疽”。1591年,fabicius Hiddanus首次发现四肢坏疽可能是静脉源性的。3.1 Haimovici2和DeBakey等人发表了一些关于硬核性痰病的优秀综述文章,因此不需要详细的文献综述。在102例文献资料中,69例发生在左下肢,27例发生在右下肢,4例发生在左上肢,2例发生在右上肢。左下肢发病率高可能是由于右髂总动脉在腹主动脉分叉后不久穿过左髂总静脉。自发性的上肢受累是罕见的,在以前的病例中仅报道过5例。这是本文的目的报告两个病例,一个与上肢受累。
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Phlegmasia Cerulea Dolens
GANGRENE and eyanosis of an extremity, due to thrombophlebitis with massive venous occlusions, is an uncommon condition and is often confused with primary arterial oeclusive disease. With massive venous occlusion and the associated arterial venospasm the blood flow may be so impeded to an extremity that cyanosis and eventually gangrene may occur. The recognition of this is important, since this gangrene is usually superficial or limited to the digits. Conservative treatment of this type of gangrene is indicated in contrast to the more radical treatment advocated for gangrene due to primary arterial insufficiency. This disease has been called "phlegmasia cerulea dolens," "blue phlebitis of Gregoire," "acute massive venous occlusion of the extremities," "pseudoembolic phlebitis, " and " gangrene of venous origin. " That gangrene of an extremity can be of venous origin was first recognized by Fabricius Hiddanus in 1593.1 Excellent review articles on phlegmasia cerulea dolens have been published by Haimovici2 auid DeBakey,3 making a detailed review of the literature unnecessary. Of the 102 cases in the literature in which information is available, 69 occurred in the left lower extremity, 27 in the right lower extremity, four in the left upper extremity, and two in the right upper extremity. The high incidence in the left lower extremity is probably because the right common iliac artery crosses over the left common iliac veini shortly after the bifurcation of the abdominal aorta. Spontaneous involvement of the upper extremity is rare, and it has been reported in only five previous cases. It is the purpose of this paper to report two cases, one with involvement of the upper extremity.
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来源期刊
CiteScore
0.30
自引率
25.00%
发文量
45
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