Astrocytoma
An astrocytoma or astrocytic hamartoma is a benign tumor that develops from the
astrocytes of the neuroglial tissue.
Astrocytomas are rare.
Astrocytomas belong to the phakomatoses and are
presumablycongenital disorders that develop from the layer of optic nerve
fibers. They may manifest themselves as purely ocular disorders or in
association with tuberous sclerosis (Bourneville’s disease).
Patients usually haveno
ocular symptoms. Calcifying astrocytichamartomas in the region of the basal
ganglia or ventricles can cause epilepsy and mental deficiency. An astrocytoma
in Bourneville’s disease will be associated typically with an adenoma sebaceum
in the facial skin.
Astrocytomas are either incidentalfindings in
ophthalmic examinations performed for other reasons, or they are diagnosed in
patients presenting with reduced visual acuity. Ophthalmos-copy will reveal single or multiple “mulberry” tumors one
to two pupil diame-ters in size. These will appear white and are often
calcified. The tumors are inherently fluorescent when observed in blue light in
fluorescein angiogra-phy with a blue filter.
A retinoblastoma should be excluded in children.That is usually
larger than an astrocytoma on ophthalmoscopy. A possible Toxocara canis granuloma should be confirmed or excluded by
serologicstudies.
No ophthalmologic treatment is required. The patient should
bereferred to a neurologist to exclude cerebral involvement.
These tumors rarely increase in size.
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