Clinico-histopathological and dermoscopic features of Becker nevus: an analytical observational study from southwestern India

Ankita D Patil, Ajay Mahaputra Kumar, Kalyan Dalave, M. Deora, Devayani Pol
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Abstract

Background: Becker nevus (BN), a common nevoid hamartoma, presents as a hypermelanotic often hypertrichotic plaque localized to the chest, shoulder, or back in the first two decades of life. Aims: The aim of the study was to evaluate clinicohistopathological and dermoscopic findings of BN in the Indian population. Methods: Thirty-five clinically diagnosed cases of BN were enrolled. Sample characteristics, clinicohistopathological findings, dermoscopic findings, and developmental abnormalities were noted and an observational analytical study was carried out. Results: The mean age of the patients was 18.9 years and 28 (80%) were Males. BN was present since birth in 12 (34.3%), developed in the first decade in 5 (14.3%), and in the second decade in 18 (51.4%). Common sites included the chest in 10 (28.6%), the face in 8 (22.9%), and the upper limb in 7 (20%). Hypertrichosis was observed in 24 (68.6%) and acneiform lesions in 2 (5.7%). Twenty-two (62.9%) patients had right-sided lesions. No developmental abnormalities were detected. Skin biopsy findings included hyperkeratosis in 25 (71.4%), acanthosis in 32 (91.4%), elongation of rete ridges in 32 (91.4%), basal layer pigmentation in 35 (100%), and smooth muscle hyperplasia in 4 (11.1%) patients. Dermoscopic findings included reticular brown lines (pigmentation network) in 32 (91.4%), perifollicular white color (perifollicular hypopigmentation) in 27 (77.1%), skin furrow hypopigmentation in 17 (48.6%), and focal hypopigmentation in 15 (48.6%) cases. Conclusions: Onset at birth and facial lesions are common in those of Indian ethnicity, while developmental abnormalities associated with BN are infrequent.
贝克尔痣的临床组织病理学和皮肤镜特征:来自印度西南部的一项分析性观察研究
背景:贝克尔痣(Becker nevus, BN)是一种常见的痣错误瘤,表现为一种多发于胸部、肩部或背部的深色斑块。目的:本研究的目的是评估印度人群BN的临床组织病理学和皮肤镜检查结果。方法:选取35例临床诊断为BN的患者。我们记录了样本特征、临床组织病理学结果、皮肤镜检查结果和发育异常,并进行了观察性分析研究。结果:患者平均年龄18.9岁,男性28例(80%)。12人(34.3%)自出生以来就存在BN, 5人(14.3%)在第一个十年发展,18人(51.4%)在第二个十年发展。常见部位包括胸部10例(28.6%),面部8例(22.9%),上肢7例(20%)。多毛24例(68.6%),针状病变2例(5.7%)。22例(62.9%)患者有右侧病变。未发现发育异常。皮肤活检结果包括角化过度25例(71.4%),棘层增生32例(91.4%),网脊伸长32例(91.4%),基底层色素沉着35例(100%),平滑肌增生4例(11.1%)。皮镜检查结果包括网状棕色纹(色素沉着网)32例(91.4%),毛囊周围白色(毛囊周围色素沉着)27例(77.1%),皮肤皱纹色素沉着17例(48.6%),局灶性色素沉着15例(48.6%)。结论:出生时发病和面部病变在印度裔人群中很常见,而与BN相关的发育异常并不常见。
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