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klippel trenaunay stroke

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https://www.readbyqxmd.com/read/23830597/coincidence-of-ischemic-stroke-and-recurrent-brain-haemorrhage-in-a-patient-with-klippel-trenaunay-syndrome
#1
Lena A Beume, Silke C Fuhrmann, Matthias Reinhard, Andreas Harloff
Cerebrovascular manifestations in Klippel-Trenaunay Syndrome (KTS) have been reported but are extremely rare. Case reports describe brain embolism in KTS-associated coagulopathy as well as bleeding due to arteriovenous malformations. We describe a 45-year-old patient with KTS and both acute ischemic stroke and repeated cerebral haemorrhage. The underlying aetiology of both events remained undetermined despite extensive diagnostic work-up, including coagulation tests and dynamic MR angiography. It is most likely that both a pathological coagulation and increased vessel fragility comparable to amyloid angiopathy were responsible for the combined brain lesions in this patient...
October 2013: Journal of Clinical Neuroscience: Official Journal of the Neurosurgical Society of Australasia
https://www.readbyqxmd.com/read/22342818/recurrent-cerebral-infarction-in-klippel-trenaunay-weber-syndrome
#2
Dimitri Renard, Aurore Larue, Guillaume Taieb, Luc Jeanjean, Pierre Labauge
No abstract text is available yet for this article.
September 2012: Clinical Neurology and Neurosurgery
https://www.readbyqxmd.com/read/21500200/thrombus-in-transit-within-a-patent-foramen-ovale-an-argument-for-consideration-of-prophylactic-closure
#3
Vincent Chow, William Wang, Michael Wilson, John Yiannikas
Recurrent pulmonary embolism (PE) in prothrombotic patients with patent foramen ovale (PFO) is not considered a setting for elective PFO closure. We describe a 35-year-old woman with known PFO, recurrent PE on warfarin, and Klippel-Trenaunay syndrome-a condition with predisposition for thromboembolism-who suffered concurrent saddle PE and devastating stroke with further impending paradoxical embolus across the PFO. Optimal management in patients with biatrial thromboembolus caught in transit across PFO is challenging...
February 2012: Journal of Clinical Ultrasound: JCU
https://www.readbyqxmd.com/read/21245639/paradoxical-brain-embolism-with-klippel-trenaunay-syndrome
#4
Kenichiro Sakai, Kensaku Sibazaki, Kazumi Kimura, Kazuto Kobayashi, Noriko Matsumoto, Yasuyuki Iguchi
Cerebrovascular diseases in patients with Klippel-Trenaunay Syndrome (KTS) are uncommon, and the mechanism of stroke has remained elusive. We describe a patient with KTS who experienced a transient ischemic attack (TIA). Contrast-transcranial Doppler with the Valsalva maneuver revealed a right-to-left shunt and contrast-transesophageal echocardiography confirmed patent foramen ovale. Ultrasonography revealed dilated superficial and deep veins in the lower extremities; the D-dimer level was high and indicated hypercoagulability...
2011: Internal Medicine
https://www.readbyqxmd.com/read/20818576/atypical-conduction-aphasia-and-the-right-hemisphere-cross-hemispheric-plasticity-of-phonology-in-a-developmentally-dyslexic-and-dysgraphic-patient-with-early-left-frontal-damage
#5
Marcelo L Berthier, Guadalupe Dávila, Natalia García-Casares, Cristina Green, Rocío Juárez, Rafael Ruiz-Cruces, J Pablo Lara, M A Barbancho
We report the rare case of a patient, JNR, with history of mixed handedness, developmental dyslexia, dysgraphia, and attentional deficits associated with a Klippel-Trenaunay syndrome and a small subcortical frontal lesion involving the left arcuate fasciculus. In adulthood, he suffered a large right perisylvian stroke and developed atypical conduction aphasia with deficits in input and output phonological processing and poor auditory-verbal short-term memory. Lexical-semantic processing for single words was intact, but he was unable to access meaning in sentence comprehension and repetition...
2011: Neurocase
https://www.readbyqxmd.com/read/20561493/pediatric-and-inherited-neurovascular-diseases
#6
REVIEW
Monique J Vanaman, Shawn L Hervey-Jumper, Cormac O Maher
Pediatric and inherited neurovascular syndromes have diverse presentations and treatments. Although many of these diseases are uncommon, they must be included in the differential diagnosis for children with strokes or hemorrhages. In neurosurgical practice, familial cavernous malformations, hereditary hemorrhagic telangiectasia (HHT), and moyamoya are the most frequently encountered of these diseases. In this article, we will discuss familial cavernomas and HHT, as well as more unusual entities such as PHACE(S) syndrome, Klippel-Trenaunay syndrome, Wyburn-Mason syndrome, sinus pericranii, radiation-induced vasculopathy, and blue rubber bleb nevus (BRBN) syndrome...
July 2010: Neurosurgery Clinics of North America
https://www.readbyqxmd.com/read/20404675/intracranial-aneurysms-in-klippel-trenaunay-weber-syndromes-case-report
#7
Ava Star, Christine E Fuller, Steve K Landas
OBJECTIVE: We present a comprehensive review of intracranial aneurysms in Klippel-Trenaunay and Klippel-Trenaunay-Weber syndromes (KTS/KTWS), and examine factors influencing the risks of surgery vs conservative management. CLINICAL PRESENTATION: A 58-year-old physician with KTS affecting the right extremities presented with left hemispheric cerebellar stroke and was discovered to harbor four intracranial aneurysms of the posterior circulation: fusiform mid and distal BA (2...
May 2010: Neurosurgery
https://www.readbyqxmd.com/read/18926244/-klippel-trenaunay-syndrome-associated-with-antithrombin-iii-deficiency
#8
M Grira, H Ben-Jemaa, T Lammouchi, S Benammou
Klippel-Trenaunay syndrome (KTS) is a rare phakomatosis characterized by cutaneous hemangiomata, venous varicosities and bone and soft tissue hypertrophy also of the affected limb. Central nervous system involvement is rare, arising from a malformation or from coagulation disorders. We report the case of a patient presenting a KTS with stroke. The biological assessment revealed antithrombin III deficiency. Although rare, antithrombin III deficiency should be kept in mind in KTS patients with neurological involvement...
October 2008: Revue Neurologique
https://www.readbyqxmd.com/read/16532132/congenital-and-genetic-cerebrovascular-anomalies-as-risk-factors-for-stroke-in-saudi-children
#9
Mustafa A Salih, Waleed R Murshid, Jihad N Zahraa, Abdel-Galil M Abdel-Gader, Ahmed A Al-Jarallah, Amal Y Kentab, Ibrahim A Alorainy, Hamdy H Hassan, Giap T Tjan
OBJECTIVE: To explore the role of and report on congenital and genetic cerebrovascular anomalies as risk factors for stroke in a prospective and retrospective cohort of Saudi children. METHODS: Children with stroke were evaluated at the Division of Pediatric Neurology (DPN), or were seen as inpatients in the Pediatric Wards at King Khalid University Hospital (KKUH), Riyadh, Kingdom of Saudi Arabia during the periods July 1992 to February 2001 (retrospective study) and February 2001 to March 2003 (prospective study)...
March 2006: Saudi Medical Journal
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