Ultrastructural characteristics of hemorrhagic, nonhemorrhagic, and recurrent cavernous malformations

被引:48
作者
Tu, J
Stoodley, MA
Morgan, MK
Storer, KP
机构
[1] Univ New S Wales, Prince Wales Med Res Inst, Kensington, NSW 2033, Australia
[2] Univ Sydney, Dept Surg, Sydney, NSW 2006, Australia
关键词
blood-brain barrier; endothelial cell; cavernous malformation; hemorrhage; recurrence;
D O I
10.3171/jns.2005.103.5.0903
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Ultrastructural characteristics of hemorrhagic, nonhemorrhagic, primary, and recurrent central nervous system cavernous malformations (CMs) were examined in an attempt to clarify their pathological mechanisms. Methods. Thirteen specimens (nine from samples of CMs and four from healthy control tissue) were processed for ultrastructural study immediately after surgical or postmortem removal, by fixation in glutaraldehyde/formalin and postfixation in OsO4. Transmission electron microscopy was used to examine the vascular walls, endothelium, subendothelium, and cytoplasmic organelles. The vascular walls in CMs demonstrated abnormal ultrastructure with no basement membranes and astrocytic foot processes. Pericytes were rarely seen. Single-layer lining endothelial cells showed fenestrated luminal surfaces. Large gaps were observed at intercellular junctions between endothelial cells, and large vesicles with extremely thin plasma membranes bordering the lumen were common in the lesions that had previously hemorrhaged. Endothelial cells of recurrent CMs had more Weibel-Palade bodies, filopodia, cytoplasmic processes, micropinocytotic vesicles, and filaments than those in primary lesions and normal control tissues. Conclusions. The absence of the blood-brain barrier, normal supporting wall structure, and large vesicles bordering the lumen of CM vessels may explain leakage of red blood cells into surrounding brain in the absence of major hemorrhage. Proliferation of residual abnormal endothelial cells may contribute to the recurrence of surgically removed CMs.
引用
收藏
页码:903 / 909
页数:7
相关论文
共 21 条
[1]   NATURAL-HISTORY OF INTRACRANIAL CAVERNOUS MALFORMATIONS [J].
AIBA, T ;
TANAKA, R ;
KOIKE, T ;
KAMEYAMA, S ;
TAKEDA, N ;
KOMATA, T .
JOURNAL OF NEUROSURGERY, 1995, 83 (01) :56-59
[2]  
Bozzola J.J., 1992, ELECT MICROSCOPY PRI, P16
[3]   Ultrastructural and immunocytochemical evidence that an incompetent blood-brain barrier is related to the pathophysiology of cavernous malformations [J].
Clatterbuck, RE ;
Eberhart, CG ;
Crain, BJ ;
Rigamonti, D .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2001, 71 (02) :188-192
[4]   KRIT1, a gene mutated in cerebral cavernous malformation, encodes a microtubule-associated protein [J].
Gunel, M ;
Laurans, MSH ;
Shin, D ;
DiLuna, ML ;
Voorhees, J ;
Choate, K ;
Nelson-Williams, C ;
Lifton, RP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (16) :10677-10682
[5]  
Gunel M, 1996, NEUROSURGERY, V38, P1265
[6]   COMPARISON OF FINE-STRUCTURE OF SMALL BLOOD-VESSELS IN INTRACRANIAL AND RETROPERITONEAL MALIGNANT LYMPHOMAS [J].
HIRANO, A ;
GHATAK, NR ;
BECKER, NH ;
ZIMMERMAN, HM .
ACTA NEUROPATHOLOGICA, 1974, 27 (02) :93-104
[7]   Developing brain cells produce factors capable of inducing the HT7 antigen, a blood-brain barrier-specific molecule, in chick endothelial cells [J].
Ikeda, E ;
Flamme, I ;
Risau, W .
NEUROSCIENCE LETTERS, 1996, 209 (03) :149-152
[8]   INTRACRANIAL CAVERNOUS MALFORMATIONS - LESION BEHAVIOR AND MANAGEMENT STRATEGIES [J].
MARAIRE, JN ;
AWAD, IA .
NEUROSURGERY, 1995, 37 (04) :591-605
[9]   Mechanisms of disease: The blood-brain barrier [J].
Neuwelt, EA .
NEUROSURGERY, 2004, 54 (01) :131-140
[10]  
OTTEN P, 1989, NEUROCHIRURGIE, V35, P82