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混合性结缔组织病(MCTD)肾脏病变的形态计量分析。

Morphometric analysis of the kidney lesions in mixed connective tissue disease (MCTD).

作者信息

Sawai T, Murakami K, Kurasono Y

机构信息

Department of Pathology, Tohoku University Hospital, Sendai, Japan.

出版信息

Tohoku J Exp Med. 1994 Oct;174(2):141-54. doi: 10.1620/tjem.174.141.

Abstract

We examined histopathological changes of the kidney in patients with mixed connective tissue disease (MCTD) including those of glomeruli, arteries and interstitium by morphometric method. All specimens examined were collected from 25 autopsy cases diagnosed as MCTD according to the criteria for this disease proposed by the MCTD committee sponsored by the Japanese government. Clinical evidence of renal dysfunction such as proteinuria was present in 16 out of 25 cases (64%). Histopathologically, membranous type glomerular lesion was found most frequently (40%), followed by membrano-proliferative (6.7%) and mesangioproliferative types (6.7%). Nine cases had no glomerular lesion. Severe arterial lesion such as necrotizing angiitis was not found in our kidney specimens. However, morphometry revealed a high incidence of intimal thickening in the renal arteries of these patients as compared to control cases, showing this to be one of the most common features of MCTD with clinical importance. This type of arterial lesion, also seen in kidneys in other types of collagen diseases, may suggest an etiology common to them. The severity of the renal interstitial lesion in MCTD was intermediate between that of systemic lupus erythematosus (SLE) and progressive systemic sclerosis (PSS), poly-or dermatomyositis (PM/DM).

摘要

我们采用形态计量学方法,研究了混合性结缔组织病(MCTD)患者肾脏的组织病理学变化,包括肾小球、动脉和间质的变化。所有检查标本均取自25例尸检病例,这些病例根据日本政府赞助的MCTD委员会提出的该病标准被诊断为MCTD。25例中有16例(64%)存在肾功能不全的临床证据,如蛋白尿。组织病理学上,膜性肾小球病变最为常见(40%),其次是膜增生性(6.7%)和系膜增生性类型(6.7%)。9例无肾小球病变。在我们的肾脏标本中未发现严重的动脉病变,如坏死性血管炎。然而,形态计量学显示,与对照病例相比,这些患者肾动脉内膜增厚的发生率较高,表明这是MCTD最常见的特征之一,具有临床重要性。这种类型的动脉病变在其他类型的胶原病肾脏中也可见,可能提示它们有共同的病因。MCTD肾间质病变的严重程度介于系统性红斑狼疮(SLE)、进行性系统性硬化症(PSS)、多肌炎或皮肌炎(PM/DM)之间。

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