Giesker D W, Pastuszak W T, Forouhar F A, Krause P J, Hine P
Am J Surg Pathol. 1982 Sep;6(6):493-501. doi: 10.1097/00000478-198209000-00001.
Kawasaki disease or mucocutaneous lymph node syndrome is an acute exanthematous illness of childhood of unknown etiology with a recent marked increase in incidence. Occasional fatalities occur usually as a result of coronary thromboarteritis. Diagnosis is based on a spectrum of clinical signs and symptoms, some of which occur late in the acute phase of the illness. We recently examined cervical lymph node biopsies from two children during the early stage of illnesses which subsequently met the clinical criteria of Kawasaki disease and in which electron microscopy, cultures, serology, and other special studies failed to identify an etiologic agent. Both lymph node biopsies revealed multiple foci of necrosis and fibrin thrombi within the microvasculature, changes which have received little attention in the pathologic literature. These pathologic alterations are distinctive and probably characteristic. Early presumptive diagnosis of Kawasaki disease in our second case was based on the histopathologic findings and resulted in prompt institution of antithrombotic therapy. Lymph node biopsy has been underutilized in the diagnosis, and characteristic acute pathologic changes which may occur have been underpublicized.
川崎病或黏膜皮肤淋巴结综合征是一种病因不明的儿童急性发疹性疾病,近年来发病率显著上升。偶尔会发生死亡,通常是冠状动脉血栓性动脉炎所致。诊断基于一系列临床体征和症状,其中一些出现在疾病急性期的后期。我们最近检查了两名儿童在疾病早期的颈部淋巴结活检样本,这两名儿童随后符合川崎病的临床标准,而电子显微镜检查、培养、血清学检查及其他特殊研究均未能确定病原体。两份淋巴结活检样本均显示微脉管系统内有多个坏死灶和纤维蛋白血栓,这些变化在病理学文献中很少受到关注。这些病理改变具有独特性,可能是该病的特征性表现。在我们的第二例病例中,基于组织病理学发现对川崎病进行了早期推测性诊断,并迅速开始了抗血栓治疗。淋巴结活检在诊断中未得到充分利用,可能出现的特征性急性病理改变也未得到充分宣传。