首页> 外文期刊>American Journal of Dermatopathology >Fibroblastic Rheumatism Versus Variant Disease of Multinucleate Cell Angiohistiocytoma
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Fibroblastic Rheumatism Versus Variant Disease of Multinucleate Cell Angiohistiocytoma

机译:肌瘤性风湿病与多核细胞血管肌细胞瘤的变异疾病

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摘要

We report an unusual case of a 49-year-old woman who presented with persistent papulonodules over bilateral fingers and inframammary region in conjunction with features of connective tissue disease including symmetrical polyarthritis and Raynaud phenomenon. Skin biopsy showed an upper-to-mid dermal proliferation of bland spindled cells with thickened collagen bundles and occasional multinucleated giant cells. Dermal blood vessels were only marginally increased. On immunohistochemistry, both the spindled cells and multinucleated giant cells stained negatively for smooth muscle actin. Some of the spindled cells stained positively with CD68 and CD163, whereas the multinucleated giant cells stained negatively for both stains. Elastic fibers were absent on elastic Van Gieson. The clinical and histopathologic features raise a diagnostic dilemma between fibroblastic rheumatism and multinucleate cell angiohistiocytoma. The patient responded well to cyclosporine and methotrexate therapy, with gradual improvement of the finger nodules.
机译:我们向一名49岁女性举行了一个不寻常的案例,该女性在双边手指和血管区域上呈现持续的幼儿组织,结合结缔组织疾病的特征,包括对称的多牙炎和雷诺现象。皮肤活组织检查显示了具有增厚胶原束和偶尔的多核巨细胞的平坦纺织细胞的高到中皮肤增殖。皮肤血管仅略微增加。在免疫组织化学中,纺织细胞和多核巨细胞均对平滑肌肌动蛋白染色。一些纺织细胞用CD68和CD163染色,而多核巨细胞对两个污渍染色。弹性van Gieson不存在弹性纤维。临床和组织病理学特征提高了纤维抑制风湿病和多核细胞血管血管细胞瘤之间的诊断困境。患者对环孢菌素和甲氨蝶呤治疗致作良好,逐渐改善手指结节。

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