Birt A R, Hogg G R
Arch Dermatol. 1979 Jun;115(6):699-702.
Sixty-four North American Indians with hereditary polymorphic light eruption (HPLE), or a family history of HPLE, had chronic, recurrent, exudative, and exfoliative cheilitis. Fifty-two had the cheilitis by the age of 10 years. Microscopically, the epithelium was either thickened, or thinned and covered by a thick crust. The dermis had a dense infiltration of inflammatory cells, mostly lymphocytes and plasma cells. The condition was not premalignant. The HPLE has to be differentiated from the chronic actinic cheilitis caused by long exposure to sunlight with out any element of hypersensitivity. The latter is potentially premalignant. Chronic recurrent actinic cheilitis associated with hereditary polymorphic light eruption appears to be a specific characteristic of photosensitivity occurring in American Indians. Plasma cell infiltration is not specific for either type of cheilitis.
64名患有遗传性多形性日光疹(HPLE)或有HPLE家族史的北美印第安人患有慢性、复发性、渗出性和剥脱性唇炎。52人在10岁时就患有唇炎。显微镜下,上皮要么增厚,要么变薄并覆盖着一层厚痂。真皮有密集的炎症细胞浸润,主要是淋巴细胞和浆细胞。这种情况并非癌前病变。HPLE必须与因长期暴露于阳光下且无任何过敏因素引起的慢性光化性唇炎相鉴别。后者有潜在的癌前病变。与遗传性多形性日光疹相关的慢性复发性光化性唇炎似乎是美洲印第安人发生的光敏性的一个特定特征。浆细胞浸润对任何一种唇炎都不具有特异性。