[Urticarial erythema with neutrophilic infiltration--correlation of cutaneous vascular changes with clinical severity].

S Kawana, K Nishioka, S Nishiyama
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Abstract

Twenty-seven cases of urticarial erythema with predominantly neutrophilic infiltration in the upper dermis were examined clinically, histologically and serologically. Their condition persisted longer than common urticaria, with transitory high fever and arthralgia being noted frequently. Based on histological examination results, the patients were divided into three groups. Ten patients with histological findings of leukocytoclastic vasculitis were diagnosed as urticarial vasculitis which was accompanied in 7 cases by systemic lupus erythematosus, Sjögren syndrome or viral hepatitis. This group frequently showed hypocomplementaemia and multiple organ involvement such as hepatitis and nephritis. An immunofluorescence study demonstrated immunoglobulin and/or complement components to be deposited in the vessel walls of upper dermis, thus implicating type III allergy in the pathogenesis. The second group consisted eight patients with moderate infiltration of neutrophils toward the vascular walls though vasculitic changes were not apparent. Systemic lupus erythematosus and Sjögren syndrome were noted in 5 of these patients but multiple organ involvement was relatively quite infrequent. Antihistamines and even systemic corticosteroids failed to have any effect in the majority of the patients on these two groups. The remaining nine patients constituting the third group showed neither neutrophilic infiltration toward vessel walls nor vascular damage and there was no multiple organ involvement. Bacterial infection of upper respiratory tract appeared to possibly be a trigger in most of these patients for whom antibiotics were effective as treatment. In conclusion, histological examination is particularly important for cases such as the present cases for accurate diagnosis and deciding appropriate treatment.

【伴有中性粒细胞浸润的荨麻疹红斑——皮肤血管变化与临床严重程度的相关性】。
本文对27例以上真皮中性粒细胞浸润为主的荨麻疹红斑进行了临床、组织学和血清学检查。他们的病情持续时间比普通荨麻疹长,并伴有短暂的高热和关节痛。根据组织学检查结果将患者分为三组。10例组织学表现为白细胞破坏性血管炎的患者诊断为荨麻疹性血管炎,其中7例合并系统性红斑狼疮、Sjögren综合征或病毒性肝炎。该组常表现为补体不足和多器官受累,如肝炎和肾炎。一项免疫荧光研究显示免疫球蛋白和/或补体成分沉积在真皮上部的血管壁上,从而暗示III型过敏的发病机制。第二组8例患者均有中性粒细胞向血管壁浸润,但血管变化不明显。5例患者有系统性红斑狼疮和Sjögren综合征,但多器官受累相对较少。抗组胺药甚至全身皮质类固醇在这两组的大多数患者中都没有任何效果。第三组的其余9例患者既没有中性粒细胞浸润到血管壁,也没有血管损伤,也没有多器官受累。上呼吸道细菌感染似乎可能是这些患者中大多数抗生素有效治疗的触发因素。总之,组织学检查对于本病例的准确诊断和决定适当的治疗尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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