Saha Abhijit, Seth Joly, Das Anupam, Dhar Sandipan
Department of Dermatology, Rita Skin Foundation, Kolkata, West Bengal, India.
Department of Dermatology, Burdwan Medical College and Hospital, Burdwan, West Bengal, India.
Int J Trichology. 2016 Oct-Dec;8(4):173-175. doi: 10.4103/0974-7753.203180.
Graham-Little-Piccardi syndrome (GLPS) is a rare form of follicular lichen planus and comprises cicatricial alopecia of the scalp, noncicatricial alopecia of the axillae, and/or pubis and spinous follicular papules involving the trunk and extremities. We herein report a classic case of GLPS in a 49-year-old female. Uniqueness of our case is due to its additional features of frontal fibrosing alopecia (FFA). Although overlap between GLPS and FFA has been mentioned in literature, such numbers are scanty. Therapeutic response with oral steroid and retinoid is also far better in contrast to what is described in the existing literature.
格雷厄姆-利特尔-皮卡迪综合征（GLPS）是一种罕见的毛囊扁平苔藓，包括头皮瘢痕性脱发、腋窝和/或耻骨部非瘢痕性脱发，以及累及躯干和四肢的棘状毛囊丘疹。我们在此报告一例49岁女性的经典GLPS病例。我们病例的独特之处在于其具有额部纤维性脱发（FFA）的额外特征。尽管文献中提到了GLPS和FFA之间的重叠，但相关病例数量很少。与现有文献中描述的情况相比，口服类固醇和维甲酸的治疗反应也要好得多。
