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多发性面部皮脂腺囊肿1例罕见病例:临床病理及皮肤镜报告

An Unusual Case of Facial Steatocystoma Multiplex: A Clinicopathologic and Dermoscopic Report.

作者信息

Sharma Aseem, Agrawal Sandip, Dhurat Rachita, Shukla Dipti, Vishwanath Tejas

机构信息

Department of Dermatology, Lokmanya Tilak Municipal Medical College (LTMMC) and Sion General Hospital, Mumbai, India.

出版信息

Dermatopathology (Basel). 2018 May 22;5(2):58-63. doi: 10.1159/000488584. eCollection 2018 Apr-Jun.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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。

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。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78f3/6031952/dd34a04ce9ac/dpa-0005-0058-g01.jpg

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