TY - JOUR
T1 - Cerebral Cavernous Malformations with Dynamic and Progressive Course
T2 - Correlation Study with Vascular Endothelial Growth Factor
AU - Jung, Keun Hwa
AU - Chu, Kon
AU - Jeong, Sang Wuk
AU - Park, Hee Kwon
AU - Bae, Hee Joon
AU - Yoon, Byung Woo
PY - 2003/11
Y1 - 2003/11
N2 - Background: Cerebral cavernous malformations (CCMs) are reported to exhibit a wide range of dynamic patterns including growth, regression, and de novo formation, which generally show slow and steady courses. Although the pathogenesis of CCMs is not well known, vascular endothelial growth factor (VEGF) has been suggested as a possible mediating factor. Objectives: To report CCMs showing rapid progression over a short period and to investigate these biological characteristics. Design: Experimental study. Setting: Tertiary referral center, neurology department. Patient: A 40-year-old man was admitted because of a left-sided numbness, vertigo, and ataxia, which were attributed to a pontine hemorrhage. He had experienced a left-sided weakness 6 months before admission, and thereafter had complained of intermittent headache. Serial brain magnetic resonance images showed multiple intracerebral microhemorrhages throughout the cerebral hemispheres. A biopsy of the lesion confirmed the diagnosis of CCM. Main Outcome Measures: We investigated the expression of VEGF by immunohistochemistry of the biopsy specimen. Dynamic patterns of CCMs, obtained with spin-echo magnetic resonance images with gradient-echo sequences, were compared with serial serum VEGF concentrations, determined by enzyme-linked immunosorbent assay. Results: Immunohistochemistry of the specimen displayed increased VEGF expression. Serial magnetic resonance images during 7 months showed dynamic signal changes of the preexisting lesions and 15 de novo formations in many cortices. The VEGF level in serum increased during this dynamic period and became normal during the steady and resolving stages. Conclusions: Cerebral cavernous malformations can be progressively deteriorating. The endothelial proliferation induced by VEGF is likely to be an important aspect of the pathogenetic mechanisms of CCMs.
AB - Background: Cerebral cavernous malformations (CCMs) are reported to exhibit a wide range of dynamic patterns including growth, regression, and de novo formation, which generally show slow and steady courses. Although the pathogenesis of CCMs is not well known, vascular endothelial growth factor (VEGF) has been suggested as a possible mediating factor. Objectives: To report CCMs showing rapid progression over a short period and to investigate these biological characteristics. Design: Experimental study. Setting: Tertiary referral center, neurology department. Patient: A 40-year-old man was admitted because of a left-sided numbness, vertigo, and ataxia, which were attributed to a pontine hemorrhage. He had experienced a left-sided weakness 6 months before admission, and thereafter had complained of intermittent headache. Serial brain magnetic resonance images showed multiple intracerebral microhemorrhages throughout the cerebral hemispheres. A biopsy of the lesion confirmed the diagnosis of CCM. Main Outcome Measures: We investigated the expression of VEGF by immunohistochemistry of the biopsy specimen. Dynamic patterns of CCMs, obtained with spin-echo magnetic resonance images with gradient-echo sequences, were compared with serial serum VEGF concentrations, determined by enzyme-linked immunosorbent assay. Results: Immunohistochemistry of the specimen displayed increased VEGF expression. Serial magnetic resonance images during 7 months showed dynamic signal changes of the preexisting lesions and 15 de novo formations in many cortices. The VEGF level in serum increased during this dynamic period and became normal during the steady and resolving stages. Conclusions: Cerebral cavernous malformations can be progressively deteriorating. The endothelial proliferation induced by VEGF is likely to be an important aspect of the pathogenetic mechanisms of CCMs.
UR - http://www.scopus.com/inward/record.url?scp=0344464846&partnerID=8YFLogxK
U2 - 10.1001/archneur.60.11.1613
DO - 10.1001/archneur.60.11.1613
M3 - Article
C2 - 14623736
AN - SCOPUS:0344464846
SN - 0003-9942
VL - 60
SP - 1613
EP - 1618
JO - Archives of Neurology
JF - Archives of Neurology
IS - 11
ER -