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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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
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author Wang, Wendy
Mack, Heather G
Stawell, Richard
White, Owen
Waterston, John
author_facet Wang, Wendy
Mack, Heather G
Stawell, Richard
White, Owen
Waterston, John
author_sort Wang, Wendy
collection PubMed
description 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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spelling pubmed-78717292021-03-04 HaNDL with bilateral central venous occlusions Wang, Wendy Mack, Heather G Stawell, Richard White, Owen Waterston, John BMJ Neurol Open Short Report 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. BMJ Publishing Group 2020-06-02 /pmc/articles/PMC7871729/ /pubmed/33681782 http://dx.doi.org/10.1136/bmjno-2020-000043 Text en © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Short Report
Wang, Wendy
Mack, Heather G
Stawell, Richard
White, Owen
Waterston, John
HaNDL with bilateral central venous occlusions
title HaNDL with bilateral central venous occlusions
title_full HaNDL with bilateral central venous occlusions
title_fullStr HaNDL with bilateral central venous occlusions
title_full_unstemmed HaNDL with bilateral central venous occlusions
title_short HaNDL with bilateral central venous occlusions
title_sort handl with bilateral central venous occlusions
topic Short Report
url 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
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AT waterstonjohn handlwithbilateralcentralvenousocclusions

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