Abstract |
The juvenile xanthogranuloma is a rare, benign, cutaneous disease occurring in infants and young children which can be situated in about 10% of the cases on the eye and preferentially on the iris. The reason for consulting an ophthalmologist is mostly a recurrent unilateral hyphemia which is typical for this disease. The diagnosis of the juvenile xanthogranuloma has to be established clinically, based on the characteristic alterations of the iris--heterochromia, vascularized tumor or diffuse thickening of the iris--and the possibly increased intraocular pressure. In order to avoid the deleting consequences of an uncontrollable secondary glaucoma, radiotherapy with a total dose of 300 to 400 cGy combined with a mild local steroid treatment has to be undertaken immediately, if possible. Taking into consideration the indications of literature, the value of a low-dose radiotherapy for this disease shall be demonstrated by five own cases in all of which the concerned eye could be healed and preserved.
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Authors | R P Müller, G Jünemann |
Journal | Strahlentherapie
(Strahlentherapie)
Vol. 159
Issue 5
Pg. 277-82
(May 1983)
ISSN: 0039-2073 [Print] Germany |
Vernacular Title | Ergebnisse der Strahlentherapie bei juvenilen Xanthogranulomen der Iris. |
PMID | 6857742
(Publication Type: Case Reports, English Abstract, Journal Article)
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Chemical References |
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Topics |
- Adrenal Cortex Hormones
(therapeutic use)
- Child, Preschool
- Female
- Granuloma
(drug therapy, radiotherapy)
- Humans
- Infant
- Iris Diseases
(drug therapy, radiotherapy)
- Male
- Radiotherapy Dosage
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