HaNDL with bilateral central venous occlusions

BACKGROUND: The syndrome of Headache and focal Neurological Deficits with cerebrospinal fluid Lymphocytosis (HaNDL) is considered a rare, idiopathic and self-limited condition. METHODS: We present a patient with HaNDL who had unique findings of florid optic disc haemorrhages from bilateral central r...

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Detalles Bibliográficos
Autores principales: Wang, Wendy, Mack, Heather G, Stawell, Richard, White, Owen, Waterston, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2020
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871729/
https://www.ncbi.nlm.nih.gov/pubmed/33681782
http://dx.doi.org/10.1136/bmjno-2020-000043
Descripción
Sumario:BACKGROUND: The syndrome of Headache and focal Neurological Deficits with cerebrospinal fluid Lymphocytosis (HaNDL) is considered a rare, idiopathic and self-limited condition. METHODS: We present a patient with HaNDL who had unique findings of florid optic disc haemorrhages from bilateral central retinal vein occlusions. RESULTS: Our patient made a full recovery with conservative management. CONCLUSION: It is important for medical attendants to recognise that HaNDL syndrome can be associated with neuro-ophthalmic complications.

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