Anita Arsovska

Rare Causes of Stroke

A Handbook
Herausgeber: Uluduz, Derya

• Broschiertes Buch

Produktbeschreibung

This book provides contemporary, practical guidance through case reports concisely summarised by global leaders in the field describing the diagnosis and treatment of rare causes of stroke, from vasculitis, hypercoagulable states, hereditary and genetic factors, cardioembolism, vasculopathies, venous occlusive conditions to bone disorders.

---

Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.

Produktdetails

• Verlag: Cambridge University Press
• Seitenzahl: 372
• Erscheinungstermin: 1. September 2022
• Englisch
• Abmessung: 157mm x 233mm x 20mm
• Gewicht: 642g
• ISBN-13: 9781108821254
• ISBN-10: 1108821251
• Artikelnr.: 63595549

Autorenporträt

Dr. Anita Arsovska is Head of Department for Urgent Neurology at the University Clinic of Neurology and Professor of Neurology at the University 'Ss Cyril and Methodius', Faculty of Medicine in Skopje, North Macedonia. Her main interests involve acute stroke management, neurosonology and neuroimaging. Prof. Arsovska is Full member of EAN, Fellow of ESO and Board member of WSO. She is current Vice-President of SAFE and Associate Commissioning Editor of WSA. Prof. Arsovska is very active in promoting stroke prevention and raising stroke awareness, organizing many public campaigns, scientific meetings and supporting European and World Stroke Day.

Inhaltsangabe

1. Inflammatory conditions
1.1.Isolated vasculitis of the central nervous system
1.2. Primary systemic vasculitis
1.2.a. Giant cell vasculitis
1.2.a.1. Temporal arteritis
1.2.a.2. Takayasu arteritis
1.2.b. Necrotising Vasculitis
1.2.b.1. Polyarteritis Nodosa(PAN)
1.2.b.2. Churg strauss syndrome
1.2.c. Granulomatosis vasculitis
1.2.c.1. Wegener granulomatosis
1.2.c.2. Lymphomatoid granulomatosis
1.2.d. Vasculitis with prominent eye movement
1.2.d.1. Susac syndrome
1.2.d.2. Vogt koyanagi harada disease
1.2.d.3. Easles disease
1.2.d.4. Cogan disease
1.3. Vasculitis secondary to systemic disease
1.3.a. Systemic lupus erythematosis
1.3.b. Behçet's disease
1.3.c. Syögren syndrome
1.3.d. Sarcoidosis
1.3.e. Inflammatory bowel disease
1.3.f. Cerebral amyloid angiopathy related
2. Infectious and postinfectious vasculitis
2.1. Meningovascular syphilis
2.2.Neuroborelliosis
2.3. Tuberculosis meningitis
2.4. Bacterial meningitis
2.5. Neurocysticercosis
2.6. VZV related: CMV and herpes infections
2.7. HIV infection
2.8. Chagas disease
3. Hypercoagulable causes of stroke
3.1. Antiphospholipid antibody syndrome
3.2. Hyperhomocysteinemia
3.3. Hyperviscosity syndrome
3.4. Disseminated intravascular coagulopathy and moschkowitz syndrome
3.5. Henoch schönlein purpura
3.6. Cancer associated stroke
4. Drug related stroke
4.1. Medication related stroke
4.2. Illicit drug related stroke
5. Hereditary and genetic causes of stroke
5.1. Genetic collagen disorders
5.1.a. Ehlerdanlos syndrome
5.1.b. Marfan syndrome
5.1.d. Neurofibromatosis
5.2. Genetic small vessel disease
5.2.a. Cerebral autosomal dominant /recessive arteriopathy with subcortical infarcts and leukoencephalopathy-CADASIL and CARASIL
5.2.b.Retinal vasculopathy with cerebral leukoencephalopathy with systemic manifestations (RVCL-S)
5.3. Genetic metabolic diseases
5.3.a. Fabry disease
5.3.b. Mitokondrial diseases
5.3.c. Menkes disease
5.3.d. Tangier disease
5.3.e. Organic acid disorders
6. Rare causes of cardioembolism
6.1. Paradoxal embolism: Patent foramen ovale
6.2. Infective Endocarditis
7. Vasospastic conditions and other vasculopathies
7.1. Reversible cerebral vasoconstriction syndrome
7.2. Eclampsia and stroke during pregnancy and postpartum
7.3. Migraine and migraine like conditions
8. Other non-inflammatory vasculopathies
8.1. Moyamoya disease
8.2. Cerebral amyloid angiopathy
8.3. Dolicoectasia and fusiform aneurysms
8.4. Carotid artery dissection
9.Venous occlusive conditions
9.1. Cerebral venous thrombosis
10.1. Bone disorders and stroke
10.2. Eagle syndrome.