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Clinical And Histopathologic Study Of Surgically Excised Mitral Valves In Children

机译:儿童手术切除二尖瓣的临床和组织病理学研究

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The present study aims to interpret the histological changes observed in surgically excised mitral valves, and to how those changes relate to the clinical criteria of valve failure. A retrospective study was performed on 25 children patients with RHD, who had mitral valve surgery between 2000 and 2004 at the GOTHI hospitals. A highly significant association was present between absence of Aschoff nodules and atrial fibrillation (p=0.0070). Mitral calcification was significantly associated with atrial fibrillation (p=0.0050), followed by double mitral dysfunction (p=0.0142). Valvular endothelial ulcerations were significantly associated with mitral stenosis (p=0.0129) and double mitral dysfunction (p=0.0100). Rheumatic heart disease continues to be an important cardiac problem afflicting the young population of Egypt. The disease has a definite effect on mitral valve microanatomy. Clinical-pathologic correlation is important in evaluating the extent of valvular affection. Introduction Rheumatic fever is an acute, systemic, partly autoimmune disease triggered by a beta-hemolytic streptococcal throat infection that cross-reacts with human tissues and may stimulate or modify immunologic responses. It is characterized by a constellation of findings that include as major manifestations: migratory polyarthritis of the large joints, carditis, subcutaneous nodules, erythema marginatum of the skin, and Syndeham chorea; the latter is a neurological disorder with involuntary purposeless, rapid movements [1,2].Rheumatic heart disease (RHD) occurs in 30 to 45% patients with rheumatic fever (RF). The incidence of RF and RHD in the tropics remains high, with a high proportion of children suffering from carditis with the first episode. The prevalence of RHD in school-age children varies considerably throughout the world. It has been reported as 0.6/1000 in the USA and 0.7/1000 in Japan, while in developing countries the prevalence rates range from 0.3/1000 to 18.6/1000. In an Egyptian study by Refat and his colleagues, the prevalence of RHD in the primary school children was 3.4/1000 [3]. Approximately 20 million cases of rheumatic fever occur in third world countries annually, with a correspondingly high incidence of advanced mitral stenosis later in life. A genetic predisposition to develop RHD appears to be important in certain countries like India, Egypt and Turkey [4]. Chronic rheumatic heart disease is the most important consequence of rheumatic fever. It is characterized principally by deforming fibrotic valvular disease (particularly mitral stenosis), which can produce permanent dysfunction and severe, sometimes fatal, cardiac dysfunction decades later [5,6]. Clinical manifestations may not be seen for years after the initial episode of rheumatic fever. The signs and symptoms of valvular disease depend on which cardiac valve(s) is(are) involved. In addition to cardiac murmurs, cardiac hypertrophy and dilation, and heart failure, patients with chronic rheumatic heart disease may suffer from arrhythmias (particularly atrial fibrillation in the setting of mitral stenosis), thromboembolic complications, and infective endocarditis. Long-term prognosis is highly variable. There may be a relentless cycle of valvular deformity yielding hemodynamic abnormality, which begets further deforming fibrosis. In addition to affecting the cardiac valves, rheumatic heart disease is a pancarditis affecting to various degrees the endocardium, myocardium, and pericardium. In some cases, rheumatic myocarditis results in cardiac dilation and progressive heart failure [7].Mitral valve leaflets are the most common structures involved in rheumatic disease; typical pathological features of rheumatic mitral disease come from acute and recurrent inflammation [8]. The rheumatic process includes leaflet thickening, calcification and retraction, perianular calcification with limitation of annular motion, leaflet fusion, chordal thickening, shortening and fusion as well
机译:本研究旨在解释在手术切除的二尖瓣中观察到的组织学变化,以及这些变化与瓣膜衰竭的临床标准之间的关系。回顾性研究了2000年至2004年之间在GOTHI医院接受二尖瓣手术的25例RHD儿童患者。在缺乏阿肖夫结节和心房颤动之间存在高度显着的关联(p = 0.0070)。二尖瓣钙化与房颤显着相关(p = 0.0050),其次是二尖瓣双功能障碍(p = 0.0142)。瓣膜内皮溃疡与二尖瓣狭窄(p = 0.0129)和二尖瓣双功能障碍(p = 0.0100)显着相关。风湿性心脏病仍然是困扰埃及年轻人的重要心脏问题。该疾病对二尖瓣显微解剖有明确的影响。临床病理相关性在评估瓣膜病变程度方面很重要。简介风湿热是一种由β-溶血性链球菌性喉炎引起的急性,全身性,部分自身免疫性疾病,与人类组织交叉反应,可能刺激或改变免疫反应。它的特征是一系列的发现,包括以下主要表现:大关节的迁徙性多关节炎,心脏炎,皮下结节,皮肤红斑和Syndeham舞蹈病;后者是一种神经性疾病,具有非自愿,无目的的快速运动[1,2]。风湿性心脏病(RHD)发生在30%至45%的风湿热(RF)患者中。在热带地区,RF和RHD的发病率仍然很高,在初发时患有心脏病的儿童比例很高。在全世界,学龄儿童的RHD患病率差异很大。据报道,在美国为0.6 / 1000,在日本为0.7 / 1000,而在发展中国家,患病率从0.3 / 1000到18.6 / 1000。 Refat和他的同事在埃及进行的一项研究中,小学生RHD的患病率为3.4 / 1000 [3]。每年在第三世界国家中约有2000万例风湿热病例,晚期生命中的二尖瓣狭窄程度较高。在某些国家,例如印度,埃及和土耳其,发展RHD的遗传易感性似乎很重要[4]。慢性风湿性心脏病是风湿热最重要的后果。它的主要特征是纤维变性的瓣膜病(尤其是二尖瓣狭窄)变形,这种疾病可在数十年后导致永久性功能障碍和严重的,有时甚至致命的心脏功能障碍[5,6]。风湿热最初发作后多年可能没有临床表现。瓣膜疾病的体征和症状取决于所涉及的心脏瓣膜。除心脏杂音,心脏肥大和扩张以及心力衰竭外,患有慢性风湿性心脏病的患者还可能患有心律不齐(特别是在二尖瓣狭窄的情况下房颤),血栓栓塞性并发症和感染性心内膜炎。长期预后变化很大。可能存在持续不断的瓣膜畸形循环,从而导致血液动力学异常,从而导致进一步的纤维化变形。除了影响心脏瓣膜外,风湿性心脏病也是一种心包膜炎,在不同程度上影响心内膜,心肌和心包膜。在某些情况下,风湿性心肌炎会导致心脏扩张和进行性心力衰竭[7]。二尖瓣小叶是风湿性疾病最常见的结构。风湿性二尖瓣疾病的典型病理特征来自急性和复发性炎症[8]。风湿病的过程包括小叶增厚,钙化和缩回,环状运动受限的周围钙化,小叶融合,弦增厚,缩短和融合

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