Department of Dermatopathology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Student of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
J Cosmet Dermatol. 2019 Feb;18(1):422-426. doi: 10.1111/jocd.12677. Epub 2018 May 23.
Distinction between alopecia areata (AA) and androgenic alopecia (AGA) can be made according to clinical presentation and biopsy findings. However, it is sometimes difficult to differentiate them, especially when the diffuse pattern of both AA and AGA is in the differential diagnosis of hair loss in androgen-dependent areas.
To evaluate the characteristics of inflammatory cell infiltration using CD3, CD4, CD8, and CD20 antigens, in AA and AGA to find some consistent histological clues for distinguishing these two entities.
A retrospective analysis of patients with diagnosed AA (30 cases) and AGA (30 cases) was performed based on the clinical and histopathological criteria. We studied immunohistochemical findings for CD3, CD4, CD8, and CD20 in all selected cases.
Immunohistochemical stains for CD4 and CD20 were not helpful in differentiating AA from AGA, but the inflammation density for AA was significantly (P-value = .025, .001) higher than AGA in CD3 (specificity= 86.7% and sensitivity= 96.7%) and CD8 (specificity= 50% and sensitivity=86.6%). Our findings revealed that intrafollicular CD3 (P-value = .017) and CD8 (P-value = ˂.001) infiltrations were significantly higher in AA samples in comparison with AGA.
Characterization of CD3 and CD8 in IHC samples is helpful, especially when the density of CD3 and CD8 T cells are significant in more than 50% of the infiltrated cells and are located intrafolliculary. Moreover, the most specific and sensitive test for differentiating of AA from AGA is CD3.
根据临床表现和活检结果,可以区分斑秃(AA)和雄激素性脱发(AGA)。然而,有时很难区分它们,尤其是在弥漫性 AA 和 AGA 模式同时存在于雄激素依赖区域脱发的鉴别诊断中。
评估使用 CD3、CD4、CD8 和 CD20 抗原的炎症细胞浸润特征,以发现一些有助于区分这两种疾病的组织学线索。
根据临床和组织病理学标准,对诊断为 AA(30 例)和 AGA(30 例)的患者进行回顾性分析。我们研究了所有选定病例的 CD3、CD4、CD8 和 CD20 的免疫组织化学发现。
CD4 和 CD20 的免疫组化染色无助于区分 AA 与 AGA,但 AA 的炎症密度明显(P 值 =.025,P 值 =.001)高于 AGA 的 CD3(特异性=86.7%,敏感性=96.7%)和 CD8(特异性=50%,敏感性=86.6%)。我们的研究结果表明,与 AGA 相比,AA 样本的毛囊内 CD3(P 值 =.017)和 CD8(P 值 <.001)浸润明显更高。
CD3 和 CD8 的 IHC 样本特征具有一定的辅助作用,特别是当超过 50%的浸润细胞中 CD3 和 CD8 T 细胞的密度显著升高且位于毛囊内时。此外,区分 AA 与 AGA 最特异和敏感的检测方法是 CD3。