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一名中年男性的获得性臂部皮肤色素沉着异常

Acquired Brachial Cutaneous Dyschromatosis in a Middle Aged Male.

作者信息

Choi Min Jung, Byun Ji Yeon, Choi Hae Young, Choi You Won

机构信息

Department of Dermatology, Ewha Womans University School of Medicine, Seoul, Korea.

出版信息

Ann Dermatol. 2018 Jun;30(3):342-344. doi: 10.5021/ad.2018.30.3.342. Epub 2018 Apr 23.

DOI:10.5021/ad.2018.30.3.342
PMID:29853750
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5929953/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e98d/5929953/1f59ecde1ced/ad-30-342-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e98d/5929953/aba0890064c1/ad-30-342-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e98d/5929953/1f59ecde1ced/ad-30-342-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e98d/5929953/aba0890064c1/ad-30-342-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e98d/5929953/1f59ecde1ced/ad-30-342-g002.jpg

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引用本文的文献

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本文引用的文献

1
Acquired brachial cutaneous dyschromatosis in a 60-year-old male: a case report and review of the literature.一名60岁男性获得性臂部皮肤色素沉着异常:病例报告及文献复习
Case Rep Dermatol Med. 2014;2014:452720. doi: 10.1155/2014/452720. Epub 2014 Dec 31.
2
Imatinib mesylate-induced hyperpigmentation of the nose and palate.甲磺酸伊马替尼引起的鼻和腭部色素沉着。
Ann Dermatol. 2014 Aug;26(4):532-3. doi: 10.5021/ad.2014.26.4.532. Epub 2014 Jul 31.
3
Acquired bilateral telangiectatic macules: a distinct clinical entity.获得性双侧毛细血管扩张性红斑:一种独特的临床实体。
JAMA Dermatol. 2014 Sep;150(9):974-7. doi: 10.1001/jamadermatol.2013.10238.
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Acquired brachial cutaneous dyschromatosis.获得性臂部皮肤色素沉着异常。
Dermatol Online J. 2011 Oct 15;17(10):16.
5
Telangiectasia macularis eruptiva perstans: a rare form of adult mastocytosis.持久性发疹性斑状毛细血管扩张症:成人肥大细胞增多症的一种罕见形式。
J Clin Aesthet Dermatol. 2011 Oct;4(10):52-4.
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Drug-induced skin pigmentation. Epidemiology, diagnosis and treatment.药物性皮肤色素沉着。流行病学、诊断与治疗。
Am J Clin Dermatol. 2001;2(4):253-62. doi: 10.2165/00128071-200102040-00006.
7
Acquired brachial cutaneous dyschromatosis: a common pigmentary disorder of the arm in middle-aged women.获得性臂部皮肤色素沉着异常:中年女性手臂常见的色素沉着紊乱。
J Am Acad Dermatol. 2000 Apr;42(4):680-4.
8
Lichen planus pigmentosus.色素性扁平苔藓
Dermatologica. 1974;149(1):43-50. doi: 10.1159/000251470.