Naim Majdy, Weyers Wolfgang, Metze Dieter
Dermatology Section, Al-Shifa Hospital, Gaza, Gaza Strip.
Am J Dermatopathol. 2011 Oct;33(7):695-704. doi: 10.1097/DAD.0b013e31820a285d.
Although exanthematous drug eruptions of the macular and papular type are common and often cause diagnostic problems, histopathologic features are not precisely defined in the literature. We present the first prospective histopathologic study of maculopapular drug eruption in 48 patients in whom the diagnosis had been made on the basis of clinical examination, history of a known offending drug, and follow-up. Because more than 1 biopsy was taken in 11 patients, 60 biopsy specimens could be examined. The most consistent epidermal features were mild spongiosis mainly of the lower layers (97% of biopsies), some hyperplasia (72%), a few lymphocytes (82%), and neutrophils (32%). The dermoepidermal junction revealed discrete vacuolization (97%), scattered lymphocytes (75%), and rare necrotic keratinocytes (32%). All cases showed a dermal perivascular inflammatory infiltrate that was superficial only in 72% of biopsies and superficial and deep in 28% of biopsies. An interstitial infiltrate in the papillary dermis could be found in 93%, more often patchy than lichenoid. In general, the perivascular infiltrate was mild and composed of lymphocytes (100%), eosinophils (60%), and neutrophils (50%). In the papillary dermis, neutrophils often outnumbered the eosinophils. Another feature were the clusters of neutrophils (38%) and eosinophils (20%) in the lumina of dilated, otherwise normal, blood vessels. Rashes induced by anticonvulsants and anxiolytics were characterized by predominance of neutrophils and largish lymphocytes. Edema of the papillary dermis was encountered frequently (85%), whereas wiry collagen bundles were an exceptional finding. In conclusion, our study defined a constellation of histopathologic findings highly suggestive of the diagnosis of exanthematous drug eruption of the macular and papular type.
尽管斑丘疹型药疹很常见,且常常引发诊断难题,但文献中对其组织病理学特征并未进行精确界定。我们开展了首例针对48例斑丘疹型药疹患者的前瞻性组织病理学研究,这些患者的诊断基于临床检查、已知致病药物史及随访情况。由于11例患者接受了不止1次活检,因此共可检查60份活检标本。最一致的表皮特征为主要累及下层的轻度海绵形成(97%的活检标本)、一些增生(72%)、少量淋巴细胞(82%)和中性粒细胞(32%)。真皮表皮交界处可见离散性空泡形成(97%)、散在淋巴细胞(75%)和罕见的坏死角质形成细胞(32%)。所有病例均显示真皮血管周围炎症浸润,仅72%的活检标本为浅层浸润,28%的活检标本为浅层及深层浸润。93%的标本可见乳头真皮间质浸润,多为斑片状而非苔藓样。总体而言,血管周围浸润较轻,由淋巴细胞(100%)、嗜酸性粒细胞(60%)和中性粒细胞(50%)组成。在乳头真皮中,中性粒细胞数量常多于嗜酸性粒细胞。另一个特征是在扩张但其他方面正常的血管腔内出现中性粒细胞簇(38%)和嗜酸性粒细胞簇(20%)。抗惊厥药和抗焦虑药引起的皮疹以中性粒细胞和较大淋巴细胞为主。乳头真皮水肿常见(85%),而致密胶原束则是罕见表现。总之,我们的研究明确了一系列高度提示斑丘疹型药疹诊断的组织病理学表现。