Optic Glioma accompanied with Somatic Overgrowth
نویسندگان
چکیده
منابع مشابه
Optic nerve glioma with complete intraocular extension
PURPOSE To present a rare presentation of optic nerve glioma (ONG) with total intraocular extension. METHODS A 44-year-old man with a history of loss of vision since childhood and recent development of progressive disfiguring proptosis was referred. RESULTS The vision in the affected eye was no light perception, and a proptosis of about 2-3 mm was present. Computed tomography and Magnetic R...
متن کاملOptic Neuritis Associated with Myelodysplastic Syndrome Accompanied by Eosinophilic Crisis.
Myelodysplastic syndrome (MDS) was diagnosed in a 64-year-old man. Three months later, he presented with right-sided visual loss. A diagnosis of optic neuritis caused by both ischemic and non-ischemic changes was established. Concurrently, prominent eosinophilia was seen in both the peripheral blood and bone marrow. A partial improvement of visual loss was obtained concomitant with a rapid decr...
متن کاملGlioma of the Optic Nerve.
Bennett.-Trans. Ophthal. Soc. U.K., Vol. XXI, p. 43, 1901. Collins.-(1) Ibid., Vol. XL, p. 406; (2) Researches Anat. and Path. of Eye, London, p. 33, 1896; (3) Trans. Ophthal Soc. U.K., Vol. XV, p. 104, 1895; (4) Ibid., Vol. XXXVI, p. 403, 1916. Dub.-Archiv f..Oihthal., Vol. XXXVII, pp. 4, 26. Duke-Elder.-Recent Advances in Ophthalmology. London, 2nd Edit., 1929. Edmunds.-Proc. Roy. Soc. Med., ...
متن کاملGlioma of the Optic Nerve.
Examination.-The left eye was markedly proptosed (Fig. 1, opposite) and displaced downwards and inwards. The ocular movements were restricted in all directions and elevation was completely absent. The lid movements were normal and the patient could close the eyevoluntarily. The conjunctival vessels were engorged. The pupil was dilated and fixed, with no perception of light. The left optic disc ...
متن کاملSomatic Overgrowth Predisposes to Seizures in Autism Spectrum Disorders
BACKGROUND Comorbidity of Autism Spectrum Disorders with seizures or abnormal EEG (Autism-Epilepsy Phenotype) suggests shared pathomechanisms, and might be a starting point to identify distinct populations within the clinical complexity of the autistic spectrum. In this study, we tried to assess whether distinct subgroups, having distinctive clinical hallmarks, emerge from this comorbid conditi...
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ژورنال
عنوان ژورنال: Clinical Pediatric Endocrinology
سال: 1996
ISSN: 0918-5739,1347-7358
DOI: 10.1297/cpe.5.supple7_66