Choi Min Jung, Byun Ji Yeon, Choi Hae Young, Choi You Won
Department of Dermatology, Ewha Womans University School of Medicine, Seoul, Korea.
Ann Dermatol. 2018 Jun;30(3):342-344. doi: 10.5021/ad.2018.30.3.342. Epub 2018 Apr 23.
Acquired brachial cutaneous dyschromatosis (ABCD) is an acquired disorder of pigmentary change that presents as chronic, asymptomatic, geographic-shaped, gray-brown patches, consisting of mixed hyper and hypopigmented macules on the dorsal aspect of the forearms. We report a case of a 40-year-old male who presented with asymptomatic, multiple brown-colored macules on the outer aspects of both arms. He had no history of hypertension and had never taken angiotensin converting enzyme inhibitors. He also denied chronic sun exposure history. Histologic examination demonstrated epidermal atrophy, increased basal layer pigmentation, and several telangiectatic vessels in the upper dermis. Solar elastosis was not remarkable. The patient's clinical and histopathologic features were consistent with a diagnosis of ABCD. Poikiloderma of Civatte, melasma, acquired bilateral telangiectatic macules and other pigmentary disorders should be considered in the differential diagnosis of ABCD. Herein, we report a case of ABCD in a middle-aged male without hypertension and medication.
获得性臂部皮肤色素沉着异常(ABCD)是一种后天性色素变化紊乱疾病,表现为慢性、无症状、地图状、灰棕色斑块,由前臂背侧混合性色素沉着过多和色素沉着过少的斑疹组成。我们报告一例40岁男性病例,其双臂外侧出现无症状的多个棕色斑疹。他无高血压病史,从未服用过血管紧张素转换酶抑制剂。他也否认有长期日晒史。组织学检查显示表皮萎缩、基底层色素沉着增加以及真皮上层有几条扩张的血管。日光性弹力组织变性不明显。患者的临床和组织病理学特征符合ABCD的诊断。在ABCD的鉴别诊断中应考虑Civatte皮肤异色病、黄褐斑、获得性双侧毛细血管扩张性斑疹及其他色素性疾病。在此,我们报告一例无高血压及用药史的中年男性ABCD病例。