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皮肤肌纤维瘤。一种发生于年轻人的良性皮肤斑块状成纤维细胞和肌成纤维细胞增生。

Dermatomyofibroma. A benign cutaneous, plaque-like proliferation of fibroblasts and myofibroblasts in young adults.

作者信息

Kamino H, Reddy V B, Gero M, Greco M A

机构信息

Department of Dermatology, New York University Medical Center, Hartford, CT.

出版信息

J Cutan Pathol. 1992 Apr;19(2):85-93. doi: 10.1111/j.1600-0560.1992.tb01348.x.

Abstract

We report nine examples of a distinct cutaneous plaque-like proliferation of fibroblasts and myofibroblasts. Eight of nine lesions were located in or around the shoulder, including axilla and upper arm. There was a predominance of women to men of 8:1. The lesions measured from 1 to 2 cm in greatest diameter. All patients were young adults (mean age 29.8 yr). All lesions involved the reticular dermis in a plaque-like fashion and extended to the upper part of the subcutaneous septa in seven cases. The lesions consisted of a proliferation of very uniform slender spindle-shaped cells arranged as well-defined elongated and intersecting fascicles with a predominantly parallel arrangement to the skin surface. There was no evidence of cytologic atypia and mitotic figures were infrequent. The spindle-shaped cells were separated by thin collagen fibers. Elastic fibers were preserved and some of them appeared thicker than normal. All adnexal structures were spared. Immunohistochemistry revealed that the cells stained positively for vimentin and muscle actin, but lacked smooth-muscle specific actin, desmin, and S-100 protein. Some dermal dendrocytes stained positively for Factor XIIIa, but the spindle-shaped cells were negative. Electron microscopy studies revealed a mixture of fibroblasts, myofibroblasts, and undifferentiated mesenchymal cells. All lesions were treated by conservative excision; follow-up information revealed no evidence of recurrence. We name this distinct lesion dermatomyofibroma. To the best of our knowledge, this entity has not been previously described in the literature.

摘要

我们报告了9例成纤维细胞和肌成纤维细胞明显的皮肤斑块样增生病例。9个病变中有8个位于肩部或其周围,包括腋窝和上臂。女性与男性的比例为8:1。病变最大直径为1至2厘米。所有患者均为年轻成年人(平均年龄29.8岁)。所有病变均以斑块样方式累及网状真皮,7例延伸至皮下间隔上部。病变由非常均匀的细长梭形细胞增生组成,排列成界限分明的细长且相互交叉的束状,主要与皮肤表面平行排列。没有细胞学异型性的证据,有丝分裂象少见。梭形细胞被薄胶原纤维分隔。弹性纤维保存完好,其中一些比正常的更粗。所有附属结构均未受累。免疫组织化学显示细胞波形蛋白和肌动蛋白染色阳性,但缺乏平滑肌特异性肌动蛋白、结蛋白和S-100蛋白。一些真皮树突状细胞因子ⅩⅢa染色阳性,但梭形细胞阴性。电子显微镜研究显示有成纤维细胞、肌成纤维细胞和未分化间充质细胞的混合。所有病变均采用保守切除治疗;随访信息显示无复发迹象。我们将这种独特的病变命名为皮肤肌纤维瘤。据我们所知,该实体此前在文献中尚未有描述。

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