Sharma Aseem, Agrawal Sandip, Dhurat Rachita, Shukla Dipti, Vishwanath Tejas
Department of Dermatology, Lokmanya Tilak Municipal Medical College (LTMMC) and Sion General Hospital, Mumbai, India.
Dermatopathology (Basel). 2018 May 22;5(2):58-63. doi: 10.1159/000488584. eCollection 2018 Apr-Jun.
Steatocystoma multiplex is a benign skin disorder originating from the sebaceous and nevoid ducts. Commonly classified under hamartomas, they are distributed over the trunk, neck, axillae, and groin.
A 28-year-old male patient complained of multiple, asymptomatic skin-colored nodules over the face of 10-year duration. Clinical examination confirmed the historic findings of nontender, polysized, flesh-colored papules and nodules over the said distribution.
On histopathology, a cyst was noted in the mid-dermis, lined by stratified squamous, agranular epithelium, which contained degenerated keratin. Nonpolarized dermoscopy showed a structureless, cream-colored area, and polarized dermoscopy revealed a distinctive, well-circumscribed, yellowish hue which was superimposed over the facial pseudoreticular pigmentary pattern. The findings were compatible with steatocystoma multiplex, and the patient was taken up for radiofrequency ablation.
Herein, we report a rare variant of steatocystoma multiplex limited to the face and scalp subjected to dermatoscopy and characteristic histological correlation. To the best of our knowledge and following a literature search, dermoscopic features of this condition have not been reported thus far.
多发性皮脂囊肿是一种起源于皮脂腺和痣样导管的良性皮肤疾病。通常归类于错构瘤,分布于躯干、颈部、腋窝和腹股沟。
一名28岁男性患者主诉面部出现多个无症状肤色结节,病程长达10年。临床检查证实了上述分布区域存在无痛、大小不一、肉色丘疹和结节的既往检查结果。
组织病理学检查显示真皮中部有一个囊肿,内衬分层鳞状无颗粒上皮,其中含有退化的角蛋白。非偏振皮肤镜检查显示为无结构的奶油色区域,偏振皮肤镜检查显示出一种独特的、边界清晰的淡黄色调,叠加在面部假网状色素沉着模式上。这些发现与多发性皮脂囊肿相符,该患者接受了射频消融治疗。
在此,我们报告了一种罕见的多发性皮脂囊肿变异型,局限于面部和头皮,并进行了皮肤镜检查及特征性组织学相关性分析。据我们所知,经文献检索,迄今为止尚未报道过这种疾病的皮肤镜特征。