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BMJ Case Rep ; 12(12)2019 Dec 08.
Article in English | MEDLINE | ID: mdl-31818899

ABSTRACT

Idiopathic hypereosinophilic syndrome (IHES) is a rare disorder. It is characterised by persistent eosinophilia with eosinophil mediated tissue infiltration and organ dysfunction. Clinical features of IHES vary widely, as it may present with dermatological, pulmonary, gastrointestinal, cardiac or neurological symptoms. We hereby report a female patient who presented with sudden onset upper limb monoplegia and after thorough investigations she was diagnosed as a case of IHES. She was managed with corticosteroids and improved with same.


Subject(s)
Hemiplegia/etiology , Hypereosinophilic Syndrome/diagnosis , Diagnosis, Differential , Female , Glucocorticoids/therapeutic use , Humans , Hypereosinophilic Syndrome/complications , Hypereosinophilic Syndrome/drug therapy , Methylprednisolone/therapeutic use , Middle Aged , Treatment Outcome , Upper Extremity/innervation
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