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作者报告22例血管免疫母细胞淋巴结病中6例合并皮肤损害,其活检显示特殊的组织象,这6例中3例皮疹与淋巴结病同时发生;另外3例发疹是在全身淋巴结病前3月至2年.皮疹的特点:3例全身红斑及斑丘疹,其中一例在发疹期间下肢出现浅溃疡;2例全身瘀点及一例全身红皮病合并四肢瘀点.4例主诉瘙痒,内有2例奇痒,用大剂量抗组织胺药物亦无效.发病与用药有关的有3例;一例因鼻窦炎服抗组织胺药2周后病情恶化,一例发病
The authors reported 22 cases of angioimmunoblastic lymphadenopathy in 6 cases with skin lesions, the biopsy showed a special organization, of these 6 cases, 3 cases of rash and lymphadenopathy at the same time; the other 3 cases of rash is in systemic lymphadenopathy 3 Month to 2 years rash characteristics: 3 cases of systemic erythema and rash, one case of ulcers in the lower extremities during rash; 2 cases of systemic petechiae and a case of erythroderma with limb extremities.4 cases complain of itching, within There are 2 cases of itching, with high-dose antihistamine is also invalid. The incidence of drug-related in 3 cases; one case of anti-histamine drugs due to sinusitis after 2 weeks of exacerbations, one case of onset