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- Multiple scrotal epidermolytic acanthomas; secondary to trauma? 多发性阴囊表皮松解性棘皮瘤:继发于外伤?
- epidermolytic acanthoma 表皮松解性棘皮瘤
- We report two cases of clear cell acanthoma. 摘要我们提出两个透明细胞棘皮瘤病例报告。
- Multiple scrotal epidermolytic acanthomas; secondary to trauma? Banky J.P. ,Turner R.J.,Hollowood K. , 多发性阴囊表皮松解性棘皮瘤:继发于外伤?
- The skin biopsy specimen showed the histologic features of epidermolytic hyperkeratosis. 病理组织检验可见到表皮裂解角质增厚的表现。
- The clinicopathologic features and family history are compatible with epidermolytic palmoplantar keratoderma. 临床病理表现及家族史都符合掌蹠表皮松解性角化症的诊断。
- Conclusion Two cases of epidermolytic hyperkeratosis ichthyosis may result from spontaneous mutation. 结论2例表皮松解性角化过度鱼鳞病可能由自发突变引起。
- Total excisions were performed and the characteristic pathologic features showed clear cell acanthoma. 手术切除后，病理下典型特徵显示透明细胞棘皮瘤。
- Epidermolytic palmoplantar keratoderma, a rare autosomal dominant hereditary disease, is a keratinization disorder of palms and soles caused by mutation in the keratin 9 gene. 掌蹠表皮松解性角化症是一罕见体显性遗传疾病，主要是因为九号角质素基因发生突变而引起掌蹠角化异常。
- acanthoma verrucosa seborrhoeica [医] 脂溢性疣状棘皮瘤, 老年疣
- epidermolytic hereditary palmoplantar keratoderma 表皮松解性遗传性掌跖皮肤角化病
- pale cell acanthoma of the scrotum 阴囊苍白细胞棘皮瘤
- epidermolytic hyperkeratotic ichthyosis 表皮松解性角化过度型鱼鳞病
- epidermolytic keratosis palmaris et plantaris 表皮松解性掌跖角化病
- hereditary epidermolytic palmoplantar keratoderma 遗传性表皮松解性掌跖角化病
- ichthyosis epidermolytic hyperkeratosis 表皮松解性角化过度鱼鳞病
- unilateral epidermolytic hyperkeratosis 单侧表皮松解性角化过度
- epidermolytic palmoplanter keratoderma 表皮松解性掌跖角化病
- Keywords ichthyosis;hyperkeratosis;epidermolytic;dwarf; 鱼鳞病;角化过度;表皮松解;侏儒;
- Keywords epidermolytic palmoplanter keratoderma;keratin 9;KRT9 gene; 表皮松解性掌跖角化病;角蛋白9;KRT9基因;
