Massone Cesare, Kodama Kazuo, Kerl Helmut, Cerroni Lorenzo
Department of Dermatology, Medical University of Graz, Graz, Austria.
Am J Surg Pathol. 2005 Apr;29(4):550-60. doi: 10.1097/01.pas.0000153121.57515.c6.
The histologic diagnosis of early mycosis fungoides (MF) is one of the most vexing problems in dermatopathology. We reviewed the histopathologic features of 745 biopsy specimens from 427 patients (male:female = 277:150; median age, 52 years; range, 3-95 years) with early (patch) lesions of MF collected from the lymphoma database of the Department of Dermatology of the Medical University of Graz (Austria). In all patients, the diagnosis was established by clinicopathologic correlation. The most common histopathologic pattern consisted of a band-like or patchy lichenoid infiltrate admixed with coarse bundles of collagen in the superficial dermis. Epidermotropism of lymphocytes was observed in most cases in one or more forms (single lymphocyte epidermotropism, 22%; basilar lymphocytes, 23%; Pautrier's microabscesses, 19%; "haloed" lymphocytes, 40%; disproportionate exocytosis, 17%; pagetoid epidermotropism, 3%). In 4% of cases, epidermotropism was completely missing. Atypical lymphocytes were present only in 9% of cases. Features of interface dermatitis were observed in 59% of cases. Other unusual findings were the presence of necrotic keratinocytes (23%), melanophages (8%), and extravasated erythrocytes (4%). In 28 patients, two or more biopsies taken on the same day at different body sites showed different histopathologic aspects, underlying the protean features of MF even in a single patient at a given time. Our study expands previous observations on histopathologic features of early lesions of MF. Although sometimes the histopathologic features are not diagnostic, they should be considered consistent with MF and do not rule out the diagnosis.
早期蕈样肉芽肿(MF)的组织学诊断是皮肤病理学中最棘手的问题之一。我们回顾了从奥地利格拉茨医科大学皮肤科淋巴瘤数据库收集的427例患者(男∶女 = 277∶150;中位年龄52岁,范围3 - 95岁)早期(斑片期)MF病变的745份活检标本的组织病理学特征。所有患者均通过临床病理相关性确诊。最常见的组织病理学模式为浅表真皮层内带状或斑片状苔藓样浸润,并伴有粗大的胶原束。多数病例观察到淋巴细胞向表皮浸润,呈一种或多种形式(单个淋巴细胞向表皮浸润,22%;基底淋巴细胞,23%;Pautrier微脓肿,19%;“晕状”淋巴细胞,40%;不成比例的外渗,17%;派杰样向表皮浸润,3%)。4%的病例完全没有向表皮浸润。仅9%的病例存在非典型淋巴细胞。59%的病例观察到界面性皮炎特征。其他不寻常的发现包括坏死角质形成细胞(23%)、噬黑素细胞(8%)和红细胞外渗(4%)。28例患者在同一天于不同身体部位进行的两次或更多次活检显示出不同的组织病理学表现,这表明即使在同一患者的特定时间,MF也具有多变的特征。我们的研究扩展了先前关于MF早期病变组织病理学特征的观察。尽管有时组织病理学特征不具有诊断性,但应认为它们与MF相符且不排除诊断。