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丘疹性弹性纤维离解:结缔组织痣的一种独特变体还是布-奥综合征的不完全形式?

Papular elastorrhexis: a distinct variant of connective tissue nevi or an incomplete form of Buschke-Ollendorff syndrome?

作者信息

Choonhakarn C, Jirarattanapochai K

机构信息

Division of Dermatology, Department of Medicine, Faculty of Medicine, Srinagarind Hospital Medical School, Khon Kaen University, Thailand.

出版信息

Clin Exp Dermatol. 2002 Sep;27(6):454-7. doi: 10.1046/j.1365-2230.2002.01051.x.

DOI:10.1046/j.1365-2230.2002.01051.x
PMID:12372083
Abstract

Papular elastorrhexis is a rare entity, possibly a form of multiple elastic tissue naevi. The cutaneous lesions in this disorder are characterized by multiple white papules usually occurring on the trunk. These tend to be nonfollicular and scattered evenly over the affected area. Histopathologically, there is a decrease of elastic fibres, that may also appear thin and fragmented. Most reported cases are sporadic but familial occurrence has been described and some authors believe that papular elastorrhexis may represent a mild form of Buschke-Ollendorff syndrome. We report an 18-year-old woman whose clinical and histopathological features were compatible with papular elastorrhexis. There was no evidence of skeletal changes or relevant family history.

摘要

丘疹性弹性组织离解是一种罕见的病症,可能是多种弹性组织痣的一种形式。该疾病的皮肤损害特征为通常出现在躯干上的多个白色丘疹。这些丘疹往往是非毛囊性的,在受累区域均匀分布。组织病理学上,弹性纤维减少,也可能显得纤细且破碎。大多数报道的病例为散发性,但也有家族性发病的描述,一些作者认为丘疹性弹性组织离解可能是布希克-奥伦多夫综合征的一种轻型表现。我们报告一例18岁女性,其临床和组织病理学特征符合丘疹性弹性组织离解。没有骨骼改变的证据或相关家族史。

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Papular elastorrhexis: clinical perspectives.丘疹性弹性纤维离解:临床视角
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The Importance of Collagen Tissue in Papular Elastorrhexis, Eruptive Collagenoma, and Nevus Anelasticus.胶原组织在丘疹性弹力纤维离解、发疹性胶原瘤和弹力纤维痣中的重要性。
Ann Dermatol. 2016 Apr;28(2):210-5. doi: 10.5021/ad.2016.28.2.210. Epub 2016 Mar 31.
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A case of papular elastorrhexis.丘疹性弹力纤维松解症1例。
Postepy Dermatol Alergol. 2016 Feb;33(1):70-2. doi: 10.5114/pdia.2016.57766. Epub 2016 Feb 29.
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Papular elastorrhexis: a case and differential diagnosis.丘疹性弹力纤维破碎:1例病例及鉴别诊断
Ann Dermatol. 2011 Sep;23 Suppl 1(Suppl 1):S53-6. doi: 10.5021/ad.2011.23.S1.S53. Epub 2011 Sep 30.