CLC number: R651.1
On-line Access: 2024-08-27
Received: 2023-10-17
Revision Accepted: 2024-05-08
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Cited: 16
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ZHAN Ren-ya, TONG Ying, SHEN Jian-feng, LANG E., PREUL C., HEMPELMANN R.G., HUGO H.H., BUHL R., BARTH H., KLINGE H., MEHDORN H.M.. Study of clinical features of amyloid angiopathy hemorrhage and hypertensive intracerebral hemorrhage[J]. Journal of Zhejiang University Science A, 2004, 5(10): 1262-1269.
@article{title="Study of clinical features of amyloid angiopathy hemorrhage and hypertensive intracerebral hemorrhage",
author="ZHAN Ren-ya, TONG Ying, SHEN Jian-feng, LANG E., PREUL C., HEMPELMANN R.G., HUGO H.H., BUHL R., BARTH H., KLINGE H., MEHDORN H.M.",
journal="Journal of Zhejiang University Science A",
volume="5",
number="10",
pages="1262-1269",
year="2004",
publisher="Zhejiang University Press & Springer",
doi="10.1631/jzus.2004.1262"
}
%0 Journal Article
%T Study of clinical features of amyloid angiopathy hemorrhage and hypertensive intracerebral hemorrhage
%A ZHAN Ren-ya
%A TONG Ying
%A SHEN Jian-feng
%A LANG E.
%A PREUL C.
%A HEMPELMANN R.G.
%A HUGO H.H.
%A BUHL R.
%A BARTH H.
%A KLINGE H.
%A MEHDORN H.M.
%J Journal of Zhejiang University SCIENCE A
%V 5
%N 10
%P 1262-1269
%@ 1869-1951
%D 2004
%I Zhejiang University Press & Springer
%DOI 10.1631/jzus.2004.1262
TY - JOUR
T1 - Study of clinical features of amyloid angiopathy hemorrhage and hypertensive intracerebral hemorrhage
A1 - ZHAN Ren-ya
A1 - TONG Ying
A1 - SHEN Jian-feng
A1 - LANG E.
A1 - PREUL C.
A1 - HEMPELMANN R.G.
A1 - HUGO H.H.
A1 - BUHL R.
A1 - BARTH H.
A1 - KLINGE H.
A1 - MEHDORN H.M.
J0 - Journal of Zhejiang University Science A
VL - 5
IS - 10
SP - 1262
EP - 1269
%@ 1869-1951
Y1 - 2004
PB - Zhejiang University Press & Springer
ER -
DOI - 10.1631/jzus.2004.1262
Abstract: Objective: The purpose of this study was to differentiate between cerebral amyloid angiopathy (CAA) and hypertension (HTN) based on hemorrhage pattern interpretation. Methods: From June 1994 to Oct., 2000, 83 patients admitted to our service with acute intracerebral hemorrhage (ICH) were investigated retrospectively; 41 patients with histologically proven diagnosis of cerebral amyloid angiography and 42 patients with clear history of hypertension were investigated. Results: Patients with a CAA-related ICH were significantly older than patients with a HTN-related ICH (74.0 years vs 66.5 years, P<0.05). There was a significantly higher number of hematomas≥30 ml in CAA (85.3%) when compared with HTN (59.5%). No basal ganglional hemorrhage was seen in CAA, but in 40.5% in HTN. In CAA-related ICH, subarachnoid hemorrhage (SAH) was seen in 26 patients (63.4%) compared to only 11 patients (26.2%) in HTN-related ICH. Intraventricular hemorrhage was seen in 24.4% in CAA, and in 26.2% in HTN. Typical features of CAA-related ICH included lobar distribution affecting mainly the lobar superficial areas, lobulated appearance, rupture into the subarachnoid space, and secondary IVH from the lobar hemorrhage. More specifically, multiplicity of hemorrhage, bilaterality, and repeated episodes also strongly suggest the diagnosis of CAA. Multiple hemorrhages, defined as 2 or more separate hematomas in multiple lobes, accounted for 17.1% in CAA-related ICH. Conclusion: There are certain features in CAA on CT and MRI and in clinical settings. To some extent, these features may contribute to distinguishing CAA from HTN related ICH.
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