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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

慢性硬膜下血腫の成因: 被膜の光顕および電顕像より見た血腫増大機序について

http://hdl.handle.net/2297/40407
http://hdl.handle.net/2297/40407
a9b3f919-9dba-4089-89ed-e25847b29d36
名前 / ファイル ライセンス アクション
ME-PR-YAMASHIMA-T-743.pdf ME-PR-YAMASHIMA-T-743.pdf (1.1 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル 慢性硬膜下血腫の成因: 被膜の光顕および電顕像より見た血腫増大機序について
タイトル
タイトル Growing Mechanism of Chronic Subdural Hematoma: Light and Electron Microscopic Study on Outer Membranes of Chronic Subdural Hematoma
言語 en
言語
言語 jpn
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
著者 山嶋, 哲盛

× 山嶋, 哲盛

WEKO 199
e-Rad 60135077
研究者番号 60135077

山嶋, 哲盛

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下地, 隆

× 下地, 隆

WEKO 23892

下地, 隆

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駒井, 杜詩夫

× 駒井, 杜詩夫

WEKO 23893

駒井, 杜詩夫

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久保田, 紀彦

× 久保田, 紀彦

WEKO 1383
e-Rad 70092781
金沢大学研究者情報 70092781
研究者番号 70092781

久保田, 紀彦

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伊藤, 治英

× 伊藤, 治英

WEKO 23894

伊藤, 治英

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山本, 信二郎

× 山本, 信二郎

WEKO 23895

山本, 信二郎

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書誌情報 Neurologia medico-chirurgica = 神経外科

巻 18-pt2, 号 10, p. 743-752, 発行日 1978-01-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0470-8105
NCID
収録物識別子タイプ NCID
収録物識別子 AA1202239X
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.2176/nmc.18pt2.743
出版者
出版者 日本脳神経外科学会 = The Japan Neurosurgical Society
抄録
内容記述タイプ Abstract
内容記述 The authors report the role of local inflammatory mechanisms in outer membranes to define the physiopathogenesis of the chronic subdural hematoma enlargement. The outer membranes in 20 adult patients of chronic subdural hematoma were investigated by means of light and electron microscopy. Microscopically, perivascular small hemorrhage and hemosiderin as well as fibroblasts, hemosiderin-laden macrophages, eosinophiles and plasma cells were found around the sinusoidal channels. Perisinusoidal hemorrhage, especially red blood cells were, usually, separated from the hematoma cavity by the fibrous layer. Several sinusoids could be seen coalesced to form multiple small cavities in outer membranes, with a fibroblast like lining. Such small hemorrhagic cavities, although not often, may rupture to communicate with the hematoma cavity. Ultrastructurally, the endothelial cells of sinusoids were rich in organelles, especially rough E.R., free ribosomes, mitochondrias, pinocytotic vesicles, and endothelial specific bodies. The site of vascular leakage was identified in several sinusoids as an endothelial gap, in the range of 1-8 μ in diameter, presumably formed by separation at intercellular junctions. Perivascular exudation of plasma lead to destruct the extracellular matrix of the sinusoidal layer. Extensive accumulations of endogenous amorphous material and irregularly arranged thin collagen fibers showed interstitial edema. Fibroblasts manufacture tropocollagen molecules within the activated rough E.R., which are then secreted onto the cell surface and gradually polymerized into visible microfibrils and collagen fibers. Interstitial edema, ultimately, disappears in the fibrous layer. The fibrous layer is generally characterized by numerous collagen fibers, fibroblasts, serum proteins and only a few capillaries, some of which show direct openings into the hematoma cavity. Some perivascular edematous fluid in the sinusoidal layer may pass through the fibrous layer into the hematoma cavity. Under scanning electron microscopy, red blood cells and fibrin strands or sheets were seen especially around the outlets of the fibrous layer capillaries. The results indicate that outer membranes, once developed, enlarge chronic subdural hematoma by ruptures of small hemorrhagic cavities formed in outer membranes, direct hemorrhage from the fibrous layer capillaries, and exudation of perisinusoidal edematous fluid into the hematoma cavity.
権利
権利情報 Copyright © The Japan Neurosurgical Society 日本脳神経外科学会
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連URI
識別子タイプ URI
関連識別子 https://www.jstage.jst.go.jp/browse/nmc
関連URI
識別子タイプ URI
関連識別子 http://jns.umin.ac.jp/
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