Open Access Open Access  Restricted Access Subscription Access
Open Access Open Access Open Access  Restricted Access Restricted Access Subscription Access

Paediatric Unilateral Hydrocephalus an Unusual Presentation of Endovascular Proliferative Angiopathy of Unilateral Middle Cerebral Artery


Affiliations
1 Dept of Neurosurgery, B.J Medical College, Pune, India
2 Dept of Cardiology, Ruby Hall Clinic, India
     

   Subscribe/Renew Journal


Adolescent female 11years of age had gradual onset progressive weakness, involving left upper limb. There was no history of headache, vomiting or diminishing of vision, trauma and fever. Full term normal delivery child received vaccinations as per schedule. Neurologically normal till 4 years of her age when she had two generalised seizures with loss of consciousness. Clinical and brain CT examinations showed no abnormality. Electro-encephalography & routine cerebrospinal fluid studies were normal. Considered epileptic and was kept on oral medication with carbamazepine. Only a few case reports of isolated MCA angiopathy in their initial stages have been reported. Clinically, diminutive-neurocognitive functions of the child at different stages must always be co-related with angiography studies and followed-up at least every two years. Therapeutic window-period and the time lost, play important role in the overall management and clinical outcome.

Keywords

Isolated MCA Angiopathy, Moyamoya Disease.
Subscription Login to verify subscription
User
Notifications
Font Size


  • Nelson JS.Dr. Henry Knipe and Dr Bruno Di Muzio et al. Principles and Practice of Neuro-pathology, Oxford University Press, USA.(2003) ISBN: 0195125894.
  • Takeuchi K, Shimizu 1. K. Hypoplasia of the bilateral internal carotid arteries. Brain Nerve1957; 9:37-43.
  • Suzuki J, Takaku A. Cerebrovascular “moyamoya”disease: disease showing abnormal net-like vessels in base of brain. Arch Neurol 1969; 20:288-99
  • Fukui M. Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (‘moyamoya’disease). ClinNeurolNeurosurg 1997; 99: Suppl 2:S238-S240.
  • Baba T, Houkin K, Kuroda S. Novel: epidemiological features of moyamoya disease. J NeurolNeurosurg Psychiatry 2008; 79:900-4.
  • Han DH, Kwon OK, Byun BJ, et al. A co-operative study: clinical characteristics of 334 Ko-rean patients with moyamoya disease treated at neurosurgical institutes, (1976-1994). ActaNeu-rochir (Wien) 2000;142:1263-73.
  • Nagaraja D, Verma A, Taly AB, etal.Cerebro-vascular disease in children. ActaNeu-rolScand1994 ; 90:251-5.
  • Wakai K, Tamakoshi A, Ikezaki K, et al. Epidemiological features of moyamoya disease in Japan: findings from a nationwide survey. ClinNeurolNeurosurg 1997; 99: Suppl 2:S1-S5.
  • Berenstein A, Lasjaunias P, terBrugge KG; SurgicalNeuroangiography: Clinical and Endo-vascular aspects in paediatrics Vol. 3, 2nd edition, 2010; Heidelberg: Springer-Verlag; 2004
  • Han DH, Kwon OK, Byun BJ, et al. A co-operative study: clinical characteristics of 334 Ko-rean patients with moyamoya disease treated at neurosurgical institutes,(1976-1994). ActaNeu-rochir (Wien) 2000;142: 1263-73.

Abstract Views: 174

PDF Views: 0




  • Paediatric Unilateral Hydrocephalus an Unusual Presentation of Endovascular Proliferative Angiopathy of Unilateral Middle Cerebral Artery

Abstract Views: 174  |  PDF Views: 0

Authors

R. Sangle
Dept of Neurosurgery, B.J Medical College, Pune, India
V. Nivargi
Dept of Cardiology, Ruby Hall Clinic, India

Abstract


Adolescent female 11years of age had gradual onset progressive weakness, involving left upper limb. There was no history of headache, vomiting or diminishing of vision, trauma and fever. Full term normal delivery child received vaccinations as per schedule. Neurologically normal till 4 years of her age when she had two generalised seizures with loss of consciousness. Clinical and brain CT examinations showed no abnormality. Electro-encephalography & routine cerebrospinal fluid studies were normal. Considered epileptic and was kept on oral medication with carbamazepine. Only a few case reports of isolated MCA angiopathy in their initial stages have been reported. Clinically, diminutive-neurocognitive functions of the child at different stages must always be co-related with angiography studies and followed-up at least every two years. Therapeutic window-period and the time lost, play important role in the overall management and clinical outcome.

Keywords


Isolated MCA Angiopathy, Moyamoya Disease.

References