Enoxaparin-induced Wunderlich syndrome in a young patient with anti-GAD 65-associated opsoclonus and limbic encephalitis: a rare complication in a rare disease.
BMJ Case Rep
; 14(10)2021 Oct 07.
Article
Dans Anglais
| MEDLINE | ID: covidwho-1462937
ABSTRACT
Wunderlich syndrome is a rare condition characterised by acute spontaneous non-traumatic renal haemorrhage into the subcapsular and perirenal spaces. Our case of anti-GAD65-associated autoimmune encephalitis (AE), aged 30 years, developed this complication following use of enoxaparin and was managed by selective glue embolisation of subsegmental branches of right renal cortical arteries. Our case had opsoclonus as one of the clinical manifestations, which has till now been described in only two patients of this AE. This patient received all forms of induction therapies (steroids, plasmapheresis, intravenous immunoglobulin and rituximab) following which she had good improvement in her clinical condition. The good response to immunotherapy is also a point of discussion as this has been rarely associated with anti-GAD65 AE.
Mots clés
Texte intégral:
Disponible
Collection:
Bases de données internationales
Base de données:
MEDLINE
Sujet Principal:
Troubles de la motilité oculaire
/
Encéphalite limbique
/
Encéphalite
Type d'étude:
Rapport de cas
/
Étude pronostique
Limites du sujet:
Femelle
/
Humains
langue:
Anglais
Année:
2021
Type de document:
Article
Pays d'affiliation:
Bcr-2021-244916
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