El-Darouti Mohammad A, Marzouk Salonaz A, Azzam Omar, Fawzi Marwa Mohsen, Abdel-Halim Mona R E, Zayed Amira A, Leheta Tahra M
Dermatology department, Faculty of Medicine, Cairo University, Egypt.
Eur J Dermatol. 2006 Jan-Feb;16(1):17-22.
Vitiligo is a common skin disease characterized by the presence of well circumscribed, depigmented milky white macules devoid of identifiable melanocytes. On the other hand, hypopigmented mycosis fungoides (MF) is a rare variant of MF which presents clinically as persistent hypopigmented macules and patches. Both disorders show a predominance of CD8+ T cells in tissue samples and hence the differentiation between the two diseases on clinical, histopathological and even immunohistochemical grounds may offer great difficulty. The aim of this work is to identity certain histopathological clues which might help to differentiate between the two diseases. The study included 54 patients (26 vitiligo patients and 28 patients with Hypopigmented MF). Skin biopsies were taken and examined by hematoxylin and eosin and CD3, CD4 and CD8 markers were performed for ten vitiligo and nine MF patients. We have found that epidermotropism, hydropic degeneration of basal cells, partial loss of pigment, preservation of some melanocytes, presence of lymphocytes within the papillary dermis, increased density of the dermal infiltrate and wiry fibrosis of the papillary dermal collagen were detected with a significantly higher incidence in hypopigmented MF rather than vitiligo (P-values < 0.0001, < 0.00011, < 0.00011, = 0.001, = 0.008 and = 0.001 respectively). On the other hand, focal thickening of the basement membrane, complete loss of pigmentation, total absence of melanocytes, as well as absence or sparsness of lymphocytes in the dermal papillae were seen much more frequently in vitiligo. Statistical analysis of these differences was significant with P-values < 0.00011, < 0.00011, < 0.00011, = 0.008 respectively, regarding these pathological criteria. We conclude that differentiation of hypopigmented MF from vitiligo is possible by relying on the histopathological clues described in this study. This is particularly useful in areas of the world where cost benefit is crucial.
白癜风是一种常见的皮肤病,其特征是出现边界清晰、色素脱失的乳白色斑片,且不存在可识别的黑素细胞。另一方面,色素减退性蕈样肉芽肿(MF)是MF的一种罕见变体,临床上表现为持续性色素减退斑和斑片。两种疾病在组织样本中均以CD8 + T细胞为主,因此基于临床、组织病理学甚至免疫组织化学依据来区分这两种疾病可能会有很大困难。这项工作的目的是确定某些组织病理学线索,以帮助区分这两种疾病。该研究纳入了54例患者(26例白癜风患者和28例色素减退性MF患者)。取皮肤活检组织,用苏木精和伊红染色检查,并对10例白癜风患者和9例MF患者进行CD3、CD4和CD8标记检测。我们发现,色素减退性MF中表皮内亲表皮现象、基底细胞水肿变性、部分色素脱失、部分黑素细胞保留、乳头真皮内有淋巴细胞、真皮浸润密度增加以及乳头真皮胶原呈细纤维状纤维化的发生率显著高于白癜风(P值分别<0.0001、<0.00011、<0.00011、=0.001、=0.008和=0.001)。另一方面,则在白癜风中更常出现基底膜局灶性增厚、色素沉着完全丧失、黑素细胞完全缺失以及真皮乳头中淋巴细胞缺失或稀少的情况。关于这些病理标准,对这些差异的统计分析具有显著性,P值分别<0.00011、<0.00011、<0.00011、=0.008。我们得出结论,依靠本研究中描述的组织病理学线索可以区分色素减退性MF和白癜风。这在成本效益至关重要的世界各地区尤其有用。