Slowly progressive retinal arteriovenous malformation and relative amblyopia.
نویسنده
چکیده
Ryan SJ, Wilkinson CP III, eds. Retina. St Louis, Mo: Mosby–Year Book Inc; 2001:1882-1960. 2. Campochiaro PA, Jerdan JA, Glaser BM, Cardin A, Michels RG. Vitreous aspirates from patients with proliferative vitreoretinopathy stimulate retinal pigment epithelial cell migration. Arch Ophthalmol. 1985;103:1403-1405. 3. Nguyen-Tan JQ, Thompson JT. RPE cell migration into intact vitreous body. Retina. 1989; 9:203-209. 4. Lopez PF, Yan Q, Kohen L, et al. Retinal pigment epithelial wound healing in vivo. Arch Ophthalmol. 1995;113:1437-1446. 5. Hogg PA, Grierson I, Hiscott P. Direct comparison of the migration of three cell types involved in epiretinal membrane formation. Invest Ophthalmol Vis Sci. 2002;43:2749-2757. 6. Crouch ER, Apple DJ. Posttraumatic migration of retinal pigment epithelial melanin. Am J Ophthalmol. 1974;78:251-254. 7. Hilton GF. Subretinal pigment migration: effects of cryosurgical retinal reattachment. Arch Ophthalmol. 1974;91:445-450. 8. Machemer R, LaQua H. Pigment epithelium proliferation in retinal detachment (massive periretinal proliferation). Am J Ophthalmol. 1975;80:1-23. 9. Anderson DH, Stern WH, Fisher SK, Erickson PA, Borgula GA. The onset of pigment epithelial proliferation after retinal detachment. Invest Ophthalmol Vis Sci. 1981;21:10-16. 10. Li ZY, Possin DE, Milam AH. Histology of bone spicule pigmentation in retinitis pigmentosa. Ophthalmology. 1995;102:805-816. 11. Crafoord S, Kopp ED, Seregard S, Algvere PV. Cellular migration into neural retina following implantation of melanin granules in the subretinal space. Graefes Arch Clin Exp Ophthalmol. 2000;238:682-689. 12. ChauhanDS,Marshall J.Theinterpretationofoptical coherence tomography imagesof the retina. Invest Ophthalmol Vis Sci. 1999;40:2332-2342.
منابع مشابه
Twenty-seven years follow-up of a patient with congenital retinocephalofacial vascular malformation syndrome and additional congenital malformations (Bonnet-Dechaume-Blanc syndrome or Wyburn-Mason syndrome)
PURPOSE Follow-up of vascular changes in a patient with congenital retinocephalofacial vascular malformation syndrome. METHODS MRI and cerebral angiography. RESULTS In a 36-year-old man, magnetic resonance imaging of the skull and cerebral angiography revealed left intracranial arteriovenous malformations. Follow-up observation of 27 years revealed no essential change of retinal and cerebra...
متن کاملArteriovenous Malformation in Temporal Lobe Presenting as Contralateral Ocular Symptoms Mimicking Carotid-Cavernous Fistula
Aim. To report a rare case of arteriovenous malformation in temporal lobe presenting as contralateral orbital symptoms mimicking carotid-cavernous fistula. Method. Interventional case report. Results. A 31-year-old Malay gentleman presented with 2-month history of painful progressive exophthalmos of his left eye associated with recurrent headache, diplopia, and reduced vision. Ocular examinatio...
متن کاملCongenital arteriovenous malformation associated with progressive hydrocephalus in a newborn.
Intracranial arteriovenous malformation is rarely presented in newborns or infants. We describe an unusual case of congenital arteriovenous malformation of the brain with multiple sequestered grape-like venous sacs presented with congenital hydrocephalus. This 4-month-old girl born with a large head, presented with progressive hydrocephalus over a period of 4 months. The brain CT showed multilo...
متن کاملA juvenile case of cerebellar arteriovenous malformation (AVM) with gradual onset of headache and ataxia.
An 11-year-old male was admitted because of frequent vomiting and truncal ataxia which had lasted for over one week. He had clear consciousness but slowly-progressive mild headache and ataxic gait. Cranial CT revealed a 4 cm hematoma in the right cerebellar hemisphere. Angiography showed a 2 x 2 cm nidus of a pial arteriovenous malformation (AVM) in the right hemisphere fed from the right poste...
متن کاملArteriovenous malformation and dementia: A case report
Arteriovenous malformation (AVM) is a congenital lesion commonly associated with intracranial hemorrhage. We describe a woman with an AVM (Spetzler-Martin grade V) and presenile progressive dementia. The association between AVM and cognition is discussed.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
- Archives of ophthalmology
دوره 122 3 شماره
صفحات -
تاریخ انتشار 2004