Bittencourt C, Ferraro D A, Soares T C B, Moraes A M, Cintra M L
Department of Pathology, Unicamp, Campinas, São Paulo, Brazil.
Clin Exp Dermatol. 2014 Dec;39(8):868-73. doi: 10.1111/ced.12406. Epub 2014 Aug 22.
Chronic telogen effluvium (CTE), a poorly understood condition, can be confused with or may be a prodrome to female pattern hair loss (FPHL). The pathogenesis of both is related to follicle cycle shortening and possibly to blood supply changes.
To analyze a number of histomorphometric and immunohistochemical findings through vascular endothelial growth factor (VEGF), Ki-67, and CD31 immunostaining in scalp biopsies of 20 patients with CTE, 17 patients with mild FPHL and 9 controls.
Ki-67 index and VEGF optical density were analyzed at the follicular outer sheath using ImageJ software. CD31 microvessel density was assessed by a Chalkley grid.
Significant follicle miniaturization and higher density of nonanagen follicles were found in FPHL, compared with patients with CTE and controls. Ki-67+ index correlated positively with FPHL histological features. The FPHL group showed the highest VEGF optical density, followed by the CTE and control groups. No differences were found in CD31 microvessel density between the three groups.
Histomorphometric results establish CTE as a distinct disorder, separate from FPHL from its outset. Its pathogenic mechanisms are also distinct. These findings support the proposed mechanism of 'immediate telogen release' for CTE, leading to cycle synchronization. For FPHL, accelerated anagen follicular mitotic rates and, thus, higher Ki-67 and VEGF values, would leave less time for differentiation, resulting in hair miniaturization.
慢性休止期脱发(CTE)是一种了解较少的病症,可能与女性型脱发(FPHL)相混淆或可能是其前驱症状。两者的发病机制均与毛囊周期缩短以及可能的血液供应变化有关。
通过对20例CTE患者、17例轻度FPHL患者和9例对照者的头皮活检组织进行血管内皮生长因子(VEGF)、Ki-67和CD31免疫染色,分析一些组织形态计量学和免疫组化结果。
使用ImageJ软件分析毛囊外鞘的Ki-67指数和VEGF光密度。通过Chalkley网格评估CD31微血管密度。
与CTE患者和对照者相比,FPHL患者存在明显的毛囊小型化和更高密度的非生长期毛囊。Ki-67+指数与FPHL组织学特征呈正相关。FPHL组的VEGF光密度最高,其次是CTE组和对照组。三组之间的CD31微血管密度没有差异。
组织形态计量学结果表明CTE从一开始就是一种与FPHL不同的独特病症。其致病机制也不同。这些发现支持了CTE的“立即休止期释放”机制,导致周期同步化。对于FPHL,生长期毛囊有丝分裂率加快,因此Ki-67和VEGF值更高,会减少分化时间,导致毛发小型化。