Literature DB >> 28111734

[A HaNDL case with papilledema mimicking transient ischemic attack].

İpek Güngör1, Arman Çakar, Elif Kocasoy Orhan, Betül Baykan.   

Abstract

The syndrome of transient headache and neurologic deficits with cerebrospinal fluid lymphocytosis (HaNDL), is a rare, benign, self-limiting syndrome that is not well known. Cerebrospinal fluid examination (CSF) on clinical suspicion has diagnostic value for this syndrome, which has a rich neurological symptomatology that can mimic many diseases causing mortality and morbidity. Although the ethiopathogenesis of this syndrome is not fully known, autoimmunity is thought to be in the foreground. Described in this article is a HaNDL case that on first clinic presentation appeared to be a transient ischemic attack (TIA) with temporary but recurring neurological findings and normal CSF pressure accompanied by papilledema. Clinical features, epidemiology, ethiopathogenesis, differential diagnosis, and treatment of this syndrome are reviewed according to the literature.

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Year:  2016        PMID: 28111734     DOI: 10.5505/agri.2015.47123

Source DB:  PubMed          Journal:  Agri        ISSN: 1300-0012


  1 in total

1.  HaNDL with bilateral central venous occlusions.

Authors:  Wendy Wang; Heather G Mack; Richard Stawell; Owen White; John Waterston
Journal:  BMJ Neurol Open       Date:  2020-06-02
  1 in total

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