Urban C, Grubbauer H M, Beitzke A, Becker H
Klin Padiatr. 1979 Jul;191(4):375-84.
Since October 1978, four cases of mucocutaneous lymph node syndrome, a disease previously not yet described in our country were observed in our childrens hospital. This particular disease has been described quite frequently in Japan since 1967. It has a characteristic manifestation being mostly benign and self limited. In a few cases however acute cardiac arrest has been described. The first case we observed expired as a result of acute coronary infarction on the twentyfifth day of illness although clinical improvement had been previously noted. At post mortem examination the coronary arteries showed changes consistent with arteriitis. The following three cases presented the more typical benign course of this disease one of them with deformities of the coronary arteries. The clinical synopsis describes the above mentioned cases.
自1978年10月以来，我院儿童医院观察到4例皮肤黏膜淋巴结综合征，这是一种我国此前尚未描述过的疾病。自1967年以来，这种特殊疾病在日本已有相当频繁的描述。它有特征性表现，大多为良性且自限性。然而，在少数病例中曾描述有急性心脏骤停。我们观察的首例病例在患病第25天因急性冠状动脉梗死死亡，尽管此前临床症状已有改善。尸检时冠状动脉显示出与动脉炎相符的变化。接下来的3例呈现出该病更典型的良性病程，其中1例有冠状动脉畸形。临床概要描述了上述病例。
