Journal article
Fibrotic racemose haemangioma of the retina.
- 2008-05-06
Published in:
- Klinische Monatsblatter fur Augenheilkunde. - 2008
English
BACKGROUND
The racemose - or arteriovenous - haemangioma of the retina is a rare developmental anomaly. It can be associated with similar vascular anomalies in other regions of the central nervous system (Wyburn-Mason syndrome).
HISTORY AND SIGNS
We report a 24-year-old woman with a chronic headache from our outpatient clinic. Other than a white tortuous strand in the retina of the right eye, which resembled a filarium at first glance, no pathologies were found. Its ends were located at the optic disc forming a sling-shaped lesion extending to the anterior nasal periphery. Partial filling was shown by fluorescence angiography. An MRI of the neurocranium detected no additional vascular abnormalities.
THERAPY AND OUTCOME
So far our patient has not suffered from any visual complaints and she will be followed up yearly.
CONCLUSIONS
We show an unusual presentation of a retinal racemose haemangioma. Diagnosis of this entity should prompt further examinations to exclude any additional haemangiomas with respect to the Wyburn-Mason syndrome.
The racemose - or arteriovenous - haemangioma of the retina is a rare developmental anomaly. It can be associated with similar vascular anomalies in other regions of the central nervous system (Wyburn-Mason syndrome).
HISTORY AND SIGNS
We report a 24-year-old woman with a chronic headache from our outpatient clinic. Other than a white tortuous strand in the retina of the right eye, which resembled a filarium at first glance, no pathologies were found. Its ends were located at the optic disc forming a sling-shaped lesion extending to the anterior nasal periphery. Partial filling was shown by fluorescence angiography. An MRI of the neurocranium detected no additional vascular abnormalities.
THERAPY AND OUTCOME
So far our patient has not suffered from any visual complaints and she will be followed up yearly.
CONCLUSIONS
We show an unusual presentation of a retinal racemose haemangioma. Diagnosis of this entity should prompt further examinations to exclude any additional haemangiomas with respect to the Wyburn-Mason syndrome.
- Language
-
- English
- Open access status
- closed
- Identifiers
-
- DOI 10.1055/s-2008-1027350
- PMID 18454409
- Persistent URL
- https://sonar.ch/global/documents/148754
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