中国麻风皮肤病杂志
中國痳風皮膚病雜誌
중국마풍피부병잡지
China journal of Leprosy and Skin Diseases
2015年
11期
670-672
,共3页
发疹性胶原瘤%鉴别诊断
髮疹性膠原瘤%鑒彆診斷
발진성효원류%감별진단
eruptive collagenoma%differential diagnosis
发疹性胶原瘤是一种罕见的结缔组织痣,本文报道3例。3例患者(男1例,女2例)均表现为多发性质韧的淡色丘疹和结节,多位于躯干部位,组织病理显示真皮浅中层胶原纤维增多致密,弹性纤维减少和断裂,患者均无家族史及合并相关疾病。
髮疹性膠原瘤是一種罕見的結締組織痣,本文報道3例。3例患者(男1例,女2例)均錶現為多髮性質韌的淡色丘疹和結節,多位于軀榦部位,組織病理顯示真皮淺中層膠原纖維增多緻密,彈性纖維減少和斷裂,患者均無傢族史及閤併相關疾病。
발진성효원류시일충한견적결체조직지,본문보도3례。3례환자(남1례,녀2례)균표현위다발성질인적담색구진화결절,다위우구간부위,조직병리현시진피천중층효원섬유증다치밀,탄성섬유감소화단렬,환자균무가족사급합병상관질병。
Eruptive collagenoma is a rare connective tissue nevi and 3 cases ( one male and two females) were reported in this article. Three patients presented with multiple firm whitish papules and nodules mainly on the trunk. There was no family history and associated systemic diseases in the tree cases. Biopsy showed con-densed collagen in the upper dermis with decreased and fragmented elastic fibers.