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Wegener肉芽肿系一少见病.现报告以皮肤损害为主的2个病例:[例1]徐××,女,38岁,1963年12月以咳嗽、气急、痰中带血起病,两肺摄片有片状阴影.继之于两手足和小腿发出黄豆大红斑、血疱,渐累及口腔及臀部,出现溃疡,反复发作.伴发热及关节酸痛.1964年5月摄片,左肺中野有巨大厚壁空洞乃收住入院.体检:体温38.2℃。两肺呼吸音粗.两眼球结膜充血。鼻粘膜水肿。双侧声带及假声带均红肿,有多处出血点,双侧披裂轻度水肿,声门运动障碍,发音嘶哑.皮损对称分布于四肢远端及臀部,均为绿豆到黄豆大暗红水肿性斑丘疹,部分为瘀斑及血
Wegener granulomatosis is a rare disease. Two cases of skin damage are reported: [Example 1] Xu × ×, female, 38 years old, December 1963 with cough, shortness of breath, bloody sputum onset, two Pulmonary radiography has flake shadows, followed by two hands and legs to produce soybeans erythema, blood blisters, gradually involving the mouth and buttocks, ulcers, recurrent fever and joint pain. May 1964 radiography, left lung Nakano has a huge thick hollow is admitted to hospital Physical examination: body temperature 38.2 ℃. Breath sounds coarse lung between the two eyes conjunctival hyperemia. Nasal mucosal edema. Bilateral vocal cord and false vocal cord are red and swollen, there are multiple bleeding points, both sides of the lesion mild edema, glottis dyskinesia, hoarse voice. Lesions symmetrical distribution in the extremities and buttocks, are mung bean to soybean dark red edema Sexual rash, part of ecchymosis and blood