Rzany B, Hering O, Mockenhaupt M, Schröder W, Goerttler E, Ring J, Schöpf E
Department of Dermatology, University of Freiburg, Germany.
Br J Dermatol. 1996 Jul;135(1):6-11.
The clinical and histopathological classification of erythema exudativum multiforme major (EEMM), Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are difficult, due to the lack of clear-cut criteria. Based on a new clinical classification, 149 of 219 (68%) histopathological specimens, from a total of 534 patients with EEMM, SJS and TEN, have been reviewed. A comparison was made with the clinical picture, and any past history of infection or drug intake. All patients had been included in the German Registry of Severe Skin Reactions between April 1990 and December 1993. No differences could be found between the biopsies examined and the total number of histopathological specimens, concerning clinical diagnosis, gender and age. Sections from 28 of 149 specimens were not diagnostic or were too old to be properly evaluated. In nine cases, other diagnoses were proposed. One hundred and eleven of the histological slides with the diagnosis of EEMM (n = 16), SJS (n = 34) and TEN (n = 61), were classified as epidermal type of erythema multiforme. In these 111 slides, necrotic keratinocytes could be found, ranging from individual cells to confluent epidermal necrosis. The epidermo-dermal junction showed changes ranging from vacuolar alteration up to subepidermal blisters. The dermal infiltrate was superficial and mostly perivascular. It was sparse in SJS and TEN, and more pronounced in EEMM. Oedema in the papillary dermis was evident occasionally in all clinical groups. In 59 of 111 cases (53%), at least one eosinophil was present in the dermis. In 11 of 111 (10%), more than 10 eosinophils per field could be seen. Eosinophils were less common in the patients with the most severe forms of TEN, in whom there was detachment of more than 30% of the skin surface area. No differences in the history for drug intake, or for infection with Mycoplasma pneumoniae, herpes simplex and other organisms, could be detected between patients with or without eosinophils in their skin sections. This dermatopathological study of patients with EEMM, SJS and TEN indicates that the epidermal type of erythema multiforme is the pathological correlate for these diseases.
重症多形红斑(EEMM)、史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)的临床及组织病理学分类存在困难,原因在于缺乏明确的标准。基于一种新的临床分类方法,对534例EEMM、SJS和TEN患者中的219例(68%)的149份组织病理学标本进行了回顾性研究。将其与临床表现以及既往的感染或用药史进行了比较。所有患者均被纳入1990年4月至1993年12月期间的德国严重皮肤反应登记处。在所检查的活检标本与组织病理学标本总数之间,在临床诊断、性别和年龄方面未发现差异。149份标本中有28份切片无法做出诊断或因年代久远而无法进行恰当评估。有9例提出了其他诊断。诊断为EEMM(n = 16)、SJS(n = 34)和TEN(n = 61)的111份组织学切片被归类为多形红斑的表皮型。在这111份切片中,可发现坏死的角质形成细胞,从单个细胞到融合性表皮坏死不等。表皮-真皮交界处的改变范围从空泡样改变到表皮下水疱形成。真皮浸润为浅层,主要是血管周围性的。在SJS和TEN中较为稀疏,而在EEMM中更为明显。在所有临床组中,偶尔可见乳头真皮水肿。在111例中的59例(53%)中,真皮中至少有一个嗜酸性粒细胞。在111例中的11例(10%)中,每视野可见超过10个嗜酸性粒细胞。在皮肤切片中有或无嗜酸性粒细胞的患者之间,在用药史或肺炎支原体、单纯疱疹及其他病原体感染史方面未检测到差异。这项对EEMM、SJS和TEN患者的皮肤病理学研究表明,多形红斑的表皮型是这些疾病的病理相关表现。