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黑色丘疹性皮病一例
引用本文:林飞燕,马寒,冯佩英,李美荣,陆春. 黑色丘疹性皮病一例[J]. 中华皮肤科杂志, 2012, 45(8): 600-602
作者姓名:林飞燕  马寒  冯佩英  李美荣  陆春
作者单位:1. 海南省海口市人民医院皮肤科2. 广州市中山大学附属第三医院皮肤科3. 4. 中山大学附属第三医院皮肤性科5. 广州中山大学第三医院皮肤科
摘    要:患者女,36岁,胸腹部多发黑褐色丘疹10余年,逐渐增多。体检:前胸、腹部皮肤可见散在数十个黑褐色扁平丘疹,直径1 ~ 3 mm,表面光滑,部分呈乳头瘤样,无融合。腹部皮损组织病理检查:表皮轻度角化过度,棘层增厚,皮突延长,互相连接成网状,棘层内可见假性角囊肿形成,基底层色素增加,真皮浅层血管周围稀疏淋巴组织细胞浸润。诊断:黑色丘疹性皮病。

关 键 词:鉴别诊断  
收稿时间:2011-09-21

Dermatosis papulosa nigra: a case report
LIN Fei-yan , MA Han , FENG Pei-ying , LI Mei-rong , LU Chun. Dermatosis papulosa nigra: a case report[J]. Chinese Journal of Dermatology, 2012, 45(8): 600-602
Authors:LIN Fei-yan    MA Han    FENG Pei-ying    LI Mei-rong    LU Chun
Abstract:A 36-year-old female presented with multiple dark brown papules on the chest and abdomen for more than 10 years, which had gradually increased in number. Physical examination revealed dozens of dark brown, flat papules measuring 1-3 mm in diameter in the chest and abdomen. Most of the lesions had a smooth surface, and some lesions gave a papilloma-like appearance, with no confluent trend. Biopsy of abdominal lesions showed mild hyperkeratosis of epidermis, acanthosis, extension of epidermal protrusions forming a reticulated appearance, horn pseudocysts in prickle cell layer, enhanced pigmentation of basal layer, and a sparse lymphocytic perivascular infiltrate in superficial dermis. A diagnosis of dermatosis papulosa nigra (DPN) was made.
Keywords:differential diagnosis  
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