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首页> 外文期刊>Pediatrics: Official Publication of the American Academy of Pediatrics >Are Infantile Periarteritis Nodosa With Coronary Artery Involvement and Fatal Mucocutaneous Lymph Node Syndrome the Same? Comparison of 20 Patients From North America With Patients From Hawaii and Japan
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Are Infantile Periarteritis Nodosa With Coronary Artery Involvement and Fatal Mucocutaneous Lymph Node Syndrome the Same? Comparison of 20 Patients From North America With Patients From Hawaii and Japan

机译:患有冠状动脉病变和致命性粘膜皮肤淋巴结综合征的小儿结节性结节炎是否相同?北美20例患者与夏威夷和日本患者的比较

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We reviewed available clinical and pathologic autopsy material from 20 patients with infantile periarteritis nodosa with coronary artery involvement (IPN) from the continental United States, two Hawaiian patients with fatal mucocutaneous lymph node syndrome (MCLS; Kawasaki disease), and three patients with classical periarteritis nodosa (CPN). Comparison of the findings in patients with IPN and in patients with MCLS from Hawaii to material from patients with fatal MCLS from Japan showed no definite clinical reason to distinguish IPN from MCLS; neither gross nor microscopic features of the vascular lesions nor their pattern of distribution appears to warrant separation of IPN from fatal MCLS. CPN differs, both clinically and pathologically, from IPN/MCLS, and may well have a different etiology.
机译:我们回顾了来自美国大陆的20例结节性小动脉结节性小结节性动脉炎(IPN)患者,两名夏威夷致命性粘膜皮肤淋巴结综合症(MCLS;川崎病)和三例经典性腹膜炎的临床和病理尸检材料结节(CPN)。将IPN患者和夏威夷MCLS患者的结果与日本致命MCLS患者的材料进行比较,没有明确的临床理由将IPN与MCLS区别开。无论是血管病变的肉眼特征还是微观特征,还是它们的分布模式都不能保证IPN与致命MCLS的分离。 CPN在临床和病理上与IPN / MCLS不同,并且病因可能会有所不同。

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