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血小板增多症中红斑性肢痛症的组织病理学

Histopathology of erythromelalgia in thrombocythaemia.

作者信息

Michiels J J, ten Kate F W, Vuzevski V D, Abels J

出版信息

Histopathology. 1984 Jul;8(4):669-78. doi: 10.1111/j.1365-2559.1984.tb02379.x.

Abstract

Erythromelalgia always appears to be an expression of thrombocythaemia which may be provoked by intravascular platelet aggregation, because it is relieved by agents interfering with platelet prostaglandin synthesis. Biopsies were taken from affected areas 1-3 weeks after discontinuation of aspirin. At that time arteriolar changes were present: the endothelial cells were often swollen with large nuclei. Narrowing of the lumen occurred by proliferation of smooth muscle cells with vacuolisation and swelling of the cytoplasm and deposition of intercellular material. The internal elastic lamina appeared to be split between the proliferated cells. This gave rise to the appearances of fibromuscular intimal arteriolar proliferation which were often occluded by thrombi of differing age. Ultimately the arterioles become completely fibrosed. These vascular changes are restricted to arterioles, are partly reversible with aspirin treatment and seem to be a characteristic of erythromelalgia.

摘要

红斑性肢痛症似乎总是血小板增多症的一种表现,这可能是由血管内血小板聚集引起的,因为它可被干扰血小板前列腺素合成的药物缓解。在停用阿司匹林1 - 3周后,从受影响区域取活检组织。那时存在小动脉变化:内皮细胞常肿大,核大。管腔狭窄是由于平滑肌细胞增殖,伴有细胞质空泡化和肿胀以及细胞间物质沉积。内弹性膜似乎在增殖细胞之间裂开。这导致了纤维肌性内膜小动脉增殖的表现,这些小动脉常被不同年龄的血栓阻塞。最终小动脉完全纤维化。这些血管变化仅限于小动脉,用阿司匹林治疗部分可逆,似乎是红斑性肢痛症的一个特征。

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