TY - JOUR
T1 - Diffusion-perfusion MR evaluation and spectroscopy before and after surgical therapy for intracerebral hemorrhage
AU - Carhuapoma, J. Ricardo
AU - Wang, Paul
AU - Beauchamp, Norman J.
AU - Hanley, Daniel F.
AU - Barker, Peter B.
N1 - Funding Information:
We thank Dr. Aziz Ulug and Dr. Peter van Zijl for the DWI sequence, and Dr. Jeff Duyn (NIH) for the MRSI sequences. Grant support: • Dr. Carhuapoma is supported in part by the DAVid A. Dana Research Prize in Neurosciences Critical Care, Johns Hopkins University School of Medicine and by the Daland Fellowship for Clinical Research Award from the American Philosophical Society. • Dr. Barker is supported by a grant from the National Institutes of Health (NIH P41RR15241). • Dr. Beauchamp is supported by a grant from the American Roentgen Ray Society. • Dr. Hanley is partially supported by a grant from the National Institutes of Health 1RO1 NS24282-08, a grant from the Food and Drug Administration Orphan Products
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2005
Y1 - 2005
N2 - Introduction: Advanced magnetic resonance imaging (MRI) techniques provide metabolic/hemodynamic information that is useful in the diagnosis of ischemic stroke. To date, however, their application in intracerebral hemorrhage (ICH) has been limited. We postulate that these MRI techniques may help define mechanisms of secondary damage and assess effects of therapeutic interventions in perihematoma tissue after ICH. Methods: A 44-year-old woman presented with severe headache resulting from a right temporal ICH. After developing neurological deterioration 5 days after the bleed, the patient underwent evacuation of the hematoma. Specimen pathology suggested the presence of a small vascular malformation. Diffusion- and perfusion-weighted imaging as well as proton magnetic resonance spectroscopic imaging (1H-MRSI) investigations to assess perihematoma brain tissue metabolic and circulatory profiles were performed before and after hematoma evacuation. Results: Pre-operative results showed mild oligemia posterior to the hematoma, increased average diffusion coefficient (DAV), and normal perihematoma N-acetyl-aspartate (NAA) concentration on 1H-MRSI. This profile was interpreted as inconsistent with ischemia (as defined by reduced DAV and NAA) but compatible with perihematoma inflammation (as defined by elevated DAV and lactate signal). Postsurgical MRI investigations showed near normalization of the perfusion deficit. Conclusion: We postulate that mass effect produced by the hematoma, and perhaps inflammation, can induce perilesional reduced cerebral perfusion in a reversible manner.
AB - Introduction: Advanced magnetic resonance imaging (MRI) techniques provide metabolic/hemodynamic information that is useful in the diagnosis of ischemic stroke. To date, however, their application in intracerebral hemorrhage (ICH) has been limited. We postulate that these MRI techniques may help define mechanisms of secondary damage and assess effects of therapeutic interventions in perihematoma tissue after ICH. Methods: A 44-year-old woman presented with severe headache resulting from a right temporal ICH. After developing neurological deterioration 5 days after the bleed, the patient underwent evacuation of the hematoma. Specimen pathology suggested the presence of a small vascular malformation. Diffusion- and perfusion-weighted imaging as well as proton magnetic resonance spectroscopic imaging (1H-MRSI) investigations to assess perihematoma brain tissue metabolic and circulatory profiles were performed before and after hematoma evacuation. Results: Pre-operative results showed mild oligemia posterior to the hematoma, increased average diffusion coefficient (DAV), and normal perihematoma N-acetyl-aspartate (NAA) concentration on 1H-MRSI. This profile was interpreted as inconsistent with ischemia (as defined by reduced DAV and NAA) but compatible with perihematoma inflammation (as defined by elevated DAV and lactate signal). Postsurgical MRI investigations showed near normalization of the perfusion deficit. Conclusion: We postulate that mass effect produced by the hematoma, and perhaps inflammation, can induce perilesional reduced cerebral perfusion in a reversible manner.
KW - Diffusion and perfusion-weighted imaging
KW - Intracerebral hemorrhage
KW - Perihematoma ischemia
KW - Proton magnetic resonance spectroscopic imaging
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U2 - 10.1385/ncc:2:1:023
DO - 10.1385/ncc:2:1:023
M3 - Article
C2 - 16174964
AN - SCOPUS:15544370699
SN - 1541-6933
VL - 2
SP - 23
EP - 27
JO - Neurocritical care
JF - Neurocritical care
IS - 1
ER -