Patterson J W, Wilkin J K, Schatzki P F
Cutis. 1985 Oct;36(4):355-8.
We recently evaluated a patient with a unique form of nodular colloid degeneration. Lesions consisted of pruritic, purpuric plaques involving the upper and lower extremities and the neck. Examination of a biopsy specimen revealed large, fissured masses of amorphous material in addition to solar elastosis. The amorphous material showed negative reactions to stains for amyloid, and other histochemical studies showed results similar to those for colloid milium. The amorphous masses demonstrated a marked positive reaction to the Verhoeff-van Gieson stain for elastin. Electron microscopic examination revealed masses of degenerated elastic tissue bordered by fibrillar material that resembled amyloid morphologically. We believe this case represents a nodular form of solar degeneration with clinical and histologic resemblances to both colloid milium and cutaneous amyloidosis.
我们最近评估了一位患有独特形式结节性胶体变性的患者。病变包括累及上下肢及颈部的瘙痒性紫癜性斑块。对活检标本的检查显示,除了日光性弹力组织变性外,还有大量裂隙状无定形物质团块。该无定形物质对淀粉样蛋白染色呈阴性反应,其他组织化学研究结果与胶体粟丘疹相似。无定形团块对弹性蛋白的Verhoeff-van Gieson染色呈明显阳性反应。电子显微镜检查显示,退化的弹性组织团块被形态上类似淀粉样蛋白的纤维状物质所包围。我们认为该病例代表了一种结节性日光性变性,在临床和组织学上与胶体粟丘疹和皮肤淀粉样变性均有相似之处。