Exploration of treatment strategies for cerebral cavernous malformations: two case reports on non-resection treatment and literature review

被引:0
作者
Han, Yibo [1 ,2 ]
Liang, Dong [1 ,3 ]
Guo, Jing [4 ]
Wang, Yibao [1 ]
Wang, Yong [1 ]
机构
[1] China Med Univ, Affiliated Hosp 1, Dept Neurosurg, Shenyang, Liaoning, Peoples R China
[2] Hamamatsu Univ Sch Med, Dept Organ & Tissue Anat, Hamamatsu, Shizuoka, Japan
[3] Hamamatsu Univ Sch Med, Dept Opt Neuroanat, Hamamatsu, Shizuoka, Japan
[4] Shenyang Renren Kangye Hosp, Shenyang, Liaoning, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2025年 / 15卷
关键词
cavernous malformations; midbrain; hydrocephalus; endoscopic third ventriculostomy; case report; NATURAL-HISTORY; BRAIN-STEM; HEMANGIOMA; ANGIOMA;
D O I
10.3389/fonc.2025.1513254
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Cavernous malformations are common vascular abnormalities of the central nervous system, but cavernous malformations of the cerebral aqueduct are rare. The choice of treatment is influenced by various factors.Case Description We report two cases of midbrain cavernous malformations. Both cases involved midbrain lesions obstructing the cerebral aqueduct, leading to obstructive hydrocephalus. The primary symptoms and complaints of the patients were related to hydrocephalus. Prior to surgery, patients underwent comprehensive imaging evaluations and received endoscopic third ventriculostomy rather than tumor resection. Both patients had favorable recoveries. We also reviewed the literature and discussed the choice of treatment strategies.Conclusion Cavernous malformations are slow-progressing central nervous system lesions with a relatively benign natural course. When selecting a treatment strategy, clinicians should carefully consider the underlying cause of the patient's primary symptoms and the specific objectives of the surgery. Avoiding overly aggressive resection that fails to address the main symptoms and potentially causes irreversible damage is crucial.
引用
收藏
页数:8
相关论文
共 48 条
[1]   Hereditary Multiple Cerebral Cavernous Malformations Associated with Wilson Disease and Multiple Lipomatosis [J].
Belousova, Olga B. ;
Okishev, Dmitry N. ;
Ignatova, Tatyana M. ;
Balashova, Maria S. ;
Boulygina, Eugenia S. .
WORLD NEUROSURGERY, 2017, 105 :1034.e1-1034.e6
[2]   Cavernous haemangioma presenting with obstructive hydrocephalus [J].
Bulluss, KJ ;
Wood, M ;
Trost, N ;
Murphy, MA .
JOURNAL OF CLINICAL NEUROSCIENCE, 2005, 12 (06) :660-663
[3]   Safety of brainstem safe entry zones: comparison of microsurgical outcomes associated with superficial, exophytic, and deep brainstem cavernous malformations [J].
Catapano, Joshua S. ;
Benner, Dimitri ;
Rhodenhiser, Emmajane G. ;
Rumalla, Kavelin ;
Graffeo, Christopher S. ;
Srinivasan, Visish M. ;
Winkler, Ethan A. ;
Lawton, Michael T. .
JOURNAL OF NEUROSURGERY, 2023, 139 (01) :113-123
[4]   SEIZURE OUTCOME AFTER LESIONECTOMY FOR CAVERNOUS MALFORMATIONS [J].
COHEN, DS ;
ZUBAY, GP ;
GOODMAN, RR .
JOURNAL OF NEUROSURGERY, 1995, 83 (02) :237-242
[5]   Multilocus linkage identifies two new loci for a Mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27 [J].
Craig, HD ;
Günel, M ;
Cepeda, O ;
Johnson, EW ;
Ptacek, L ;
Steinberg, GK ;
Ogilvy, CS ;
Berg, MJ ;
Crawford, SC ;
Scott, RM ;
Steichen-Gersdorf, E ;
Sabroe, R ;
Kennedy, CTC ;
Mettler, G ;
Beis, MJ ;
Fryer, A ;
Awad, IA ;
Lifton, RP .
HUMAN MOLECULAR GENETICS, 1998, 7 (12) :1851-1858
[6]   Tectal plate cavernoma - A special entity of brainstem cavernomas: Case report [J].
Cristini, A ;
Fischer, C ;
Sindou, M .
SURGICAL NEUROLOGY, 2004, 61 (05) :474-478
[7]   CAVERNOUS HEMANGIOMA OF THE MESENCEPHALON: TONSILLOUVEAL TRANSAQUEDUCTAL APPROACH [J].
Dammers, Ruben ;
Delwel, Ernst J. ;
Krisht, Ali F. .
NEUROSURGERY, 2009, 64 (05) :296-299
[8]   Third ventricular cavernous haemangioma [J].
Darwish, B ;
Boet, R ;
Finnis, N ;
Smith, N .
JOURNAL OF CLINICAL NEUROSCIENCE, 2005, 12 (05) :601-603
[9]   AN ANALYSIS OF THE NATURAL-HISTORY OF CAVERNOUS ANGIOMAS [J].
DELCURLING, O ;
KELLY, DL ;
ELSTER, AD ;
CRAVEN, TE .
JOURNAL OF NEUROSURGERY, 1991, 75 (05) :702-708
[10]   A GENE RESPONSIBLE FOR CAVERNOUS MALFORMATIONS OF THE BRAIN MAPS TO CHROMOSOME 7Q [J].
DUBOVSKY, J ;
ZABRAMSKI, JM ;
KURTH, J ;
SPETZLER, RF ;
RICH, SS ;
ORR, HT ;
WEBER, JL .
HUMAN MOLECULAR GENETICS, 1995, 4 (03) :453-458