Perrin C, Durant J M, Lacour J P, Michiels J F, Dellamonica P, Ortonne J P
Department of Pathology, Hopital Pasteur, Nice, France.
Am J Dermatopathol. 1993 Aug;15(4):358-62.
We present a case of pityriasis rubra pilaris (PRP)-like eruption, in association with human immunodeficiency virus (HIV) infection, clinically characterized by follicular papules with some elongated spines and comedo-like lesions. The lesions were located on the back, flanks, and proximal extremities. Orthokeratotic follicular plugs and perifollicular mucinous degeneration were consistently observed on three biopsies. The most characteristic histological features of PRP were absent. To our knowledge, this is the first reported case of this kind. Such a case could suggest an atypical PRP modified by HIV infection. It is also possible that it represents a new entity associated with advanced HIV infection (horny perifollicular mucinosis).
我们报告一例与人类免疫缺陷病毒(HIV)感染相关的红皮病型毛发红糠疹(PRP)样皮疹,其临床特征为伴有一些细长棘突的毛囊丘疹和粉刺样损害。皮损位于背部、侧腹和四肢近端。在三次活检中均持续观察到正角化性毛囊栓和毛囊周围黏液变性。PRP最具特征性的组织学特征并不存在。据我们所知,这是首例此类报告病例。这样的病例可能提示由HIV感染所致的非典型PRP。也有可能它代表一种与晚期HIV感染相关的新实体(角质化毛囊周围黏蛋白沉积症)。