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伴有嗜酸性真皮沉积的肢端角化病:一种独特的临床病理实体还是复发性胶样粟丘疹?

Acral keratosis with eosinophilic dermal deposits: a distinctive clinicopatholgic entity or colloid milium redux?

作者信息

Saeed Sadia, Sagatys Elizabeth, Morgan Michael B

机构信息

Department of Pathology, University of South Florida College of Medicine, Florida, USA.

出版信息

J Cutan Pathol. 2006 Oct;33(10):679-85. doi: 10.1111/j.1600-0560.2006.00530.x.

Abstract

AIMS

The differential diagnosis of acral keratoses is broad. Encompassing a variety of infectious, heritable and degenerative disorders, emphasis upon the clinical setting and histologic subtlety are often required to arrive at the correct diagnosis. Herein, we report on a series of adult patients who presented with agminated or solitary papules of the distal finger found on histologic examination to contain amorphous eosinophilic deposits.

RESULTS

The eosinophilic deposits were found in close proximity to the overlying epithelium and devoid of apoptotic keratinocytes, plasma cells, or vascular thickening reminiscent of amyloidosis or hyalinosis cutis. Special and immunostains yielded eosinophilic material that was elastin and Protein P negative. Despite a similar histomorphologic appearance to colloid milium, typical clinical features of this entity were not present.

CONCLUSION

The etiologic significance of this condition is unknown. Potential sources of the material and a discussion of the differential diagnosis follow.

摘要

目的

肢端角化病的鉴别诊断范围广泛。它涵盖了多种感染性、遗传性和退行性疾病,通常需要重视临床背景和组织学细微特征才能得出正确诊断。在此,我们报告一系列成年患者,其手指末端出现簇状或孤立性丘疹,组织学检查发现含有无定形嗜酸性沉积物。

结果

嗜酸性沉积物位于上皮层附近,不存在凋亡角质形成细胞、浆细胞或血管增厚,这与淀粉样变性或皮肤透明变性不同。特殊染色和免疫染色显示嗜酸性物质对弹性蛋白和蛋白P呈阴性。尽管组织形态学外观与胶样粟丘疹相似,但该疾病并无典型临床特征。

结论

这种情况的病因学意义尚不清楚。随后将讨论该物质的潜在来源及鉴别诊断。

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