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Reactive eccrine syringofibroadenomatosis secondary to primary cutaneous amyloidosis: A novel association

机译:继发于原发性皮肤淀粉样变性的反应性内分泌性纤维腺瘤病:一种新型关联

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摘要

We report the unprecedented case of reactive eccrine syringofibroadenoma (ESFA) secondary to primary cutaneous amyloidosis. A 62-year-old woman of Asian ethnicity presented with a pruritic rash on the back of long-standing duration. Physical examination revealed diffuse hyperpigmentation localized to the interscapular region; there were a multitude of hyperpigmented macules merged in a rippled pattern intermixed with scattered papules and cobblestone-like areas. A punch biopsy from a papule was taken. Histopathological examination revealed a network of epithelial strands and cords hanging from the epidermis and harboring foci of ductal differentiation. Eosinophilic collections of amorphous material were found between the epithelial strands, obscuring the superficial dermis. The microscopic picture was consistent with primary cutaneous amyloidosis associated with reactive ESFA. Results of histochemical and immunohistochemical staining confirmed the diagnosis. We speculate that pathogenetic mechanisms intrinsic to primary cutaneous amyloidosis, in addition to unknown genetic factors, resulted in clinical changes of lichen amyloidosus associated with an abnormal hyperplastic epithelial response with histopathological features of ESFA rather than the common epidermal change of acanthosis and hyperkeratosis.
机译:我们报告史无前例的继发于原发性皮肤淀粉样变性的反应性内分泌腺癌(ESFA)。一名62岁的亚裔亚裔妇女长期站立后出现瘙痒性皮疹。体格检查发现弥漫性色素沉着位于肩s间区域。有许多色素沉着的斑状斑纹融合在一起,并散布着丘疹和类似鹅卵石的区域。从丘疹进行打孔活检。组织病理学检查显示上皮链和索的网络悬挂在表皮上,并具有导管分化的灶。上皮链之间发现无定形物质的嗜酸性集合,使表层真皮模糊。显微照片与反应性ESFA相关的原发性皮肤淀粉样变性一致。组织化学和免疫组织化学染色的结果证实了诊断。我们推测,除了未知的遗传因素外,原发性皮肤淀粉样变性病固有的致病机制还导致了地衣淀粉样变性的临床变化,其与具有ESFA组织病理学特征的异常增生上皮反应有关,而不是棘皮病和角化过度的常见表皮变化。

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