نتایج جستجو برای: vascular malformation

تعداد نتایج: 233412  

Journal: :Journal of Korean Medical Science 2001
J. Y. Park J. Y. Ahn B. H. Lee R. Huh H. K. Choi M. S. Shin

Pulsatile tinnitus is a rarely occurring symptom of vascular origin. Most frequently, the symptoms are due to an arteriovenous malformation, to a tumor of the jugular glomus or to a local arterial stenosis. A 39-yr-old Korean male suffering from pulsatile tinnitus of the left ear was diagnosed to have dural arteriovenous malformation of the jugular bulb. Magnetic resonance imaging and angiograp...

Journal: :Chang Gung medical journal 2003
Vuthy Chhoeurn Glenda H de Villa Lun-Jou Lo

A mandibular arteriovenous malformation (AVM) is rare, and unawareness of this condition can lead to catastrophic complications. Embolization is an effective means to treat these lesions. The osseous changes and long-term outcomes among the pediatric patients after embolization treatment remain unclear. We present a 6-year-old patient with mandibular arteriovenous malformation who had sustained...

Journal: :Stroke 2007
Yao Zhao Yu-Zhen Tan Liang-Fu Zhou Hai-Jie Wang Ying Mao

BACKGROUND AND PURPOSE Little is known about the role of endothelial cells (ECs) in the pathogenesis of cerebral cavernous malformation because of the difficulties to obtain highly pure ECs. Thus, this study attempted to establish a reliable procedure to isolate and culture ECs from human cerebral cavernous malformation lesions. The biological features and the angiogenic potential of the cultur...

2013
Jan Hrubý Robert Novotný Miroslav Špaček Petr Mitáš Jaroslav Hlubocký David Janák Ctibor Povýšil Jaroslav Lindner

Objective. To report on a very rare case of a glomus tumor manifested on the upper arm in a healthy young male patient. Case Presentation and Intervention. A 22-year-old male patient presented with bluish multifocal venous malformation on the left upper arm and was admitted for venous malformation excision. Pain, discomfort, and upper arm paraesthesia had been present for almost 6 years. Ultras...

2013
J. J. Gold J. R. Crawford

A 9-year-old girl with a several-month history of unilateral intermittent headaches presented to the hospital with worsening headaches and unsteadiness. Neurologic exam was positive for a mild right hemiparesis and right homonymous hemianopsia. Noncontrast computed tomography revealed an engorged sagittal and straight sinus with prominent cortical veins concerning an arteriovenous malformation ...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1988
D Kondziolka B J Nixon P Lasjaunias W S Tucker K TerBrugge S M Spiegel

The common vascular anomalies of cerebral aneurysm and arteriovenous malformation may exist independently, or together as part of a closely related hemodynamic pairing. Resection or embolization of an AVM may be followed by a decrease in local blood flow, and lead to regression of a suitably situated proximal aneurysm. However, aneurysms located outside the angioarchitecture of the AVM, which r...

2014
Omar Choudhri Jeremy J. Heit Mihir Gupta Michael P. Marks Robert Dodd

We report the utility of fluorescent indocyanine green (ICG) during the microsurgical resection of a giant perimedullary cervical arteriovenous fistula (GPMAVF) in a young man with hereditary hemorrhagic telangiectasia. ICG angiography is a useful adjunct for understanding angioarchitecture and drainage patterns in spinal arteriovenous malformation (AVM) surgery. Cervical GPMAVF is a rare spina...

Journal: :Turkish neurosurgery 2013
Anuj Bahl Ashok Raghavan Saurabh Sinha

Blue rubber bleb naevus syndrome is an uncommon disorder whereby patients possess cutaneous vascular malformations. Cranial malformations have been rarely reported in the literature. We report the first ever case of a patient with blue rubber bleb naevus syndrome (BRBNS), who was found to have a symptomatic Chiari malformation and prominent subcutaneous vascular malformations in communication w...

2005
Hyung-Min Kwon Jong-Moo Park Jee-Young Lee Byung-Woo Yoon

Spontaneous primary medullary hemorrhage is a rare event. A 64-year-old man was admitted for sudden-onset vertigo and vomiting. His clinical features were similar to those of lateral medullary syndrome. The patient had no anticoagulant therapy, vascular malformation, or a caudal extension of a pontine hemorrhage. The patient had multiple hypertensive changes, including retinopathy, left ventric...

Journal: :The Turkish journal of pediatrics 2012
Elzbieta Gawrych Anna Walecka Artur Kwas Jacek Materny Marcin Sawicki

We report a rare finding of the coexistence of splenic hemangioma and progressive vascular malformation of the left lower extremity in a child. The lesion on the left calf was described as a vascular malformation in computed tomography and magnetic resonance. At the age of one year, the abdominal Doppler ultrasound was normal. The examination was repeated at the age of six years due to recurren...

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