Intrakraniel hypertension sekundært til systemisk lupus erythematosus

Abstract

Systemic lupus erythematosus (SLE) is a diagnostically challenging autoimmune multisystem disease with intracranial hypertension as a rare initial clinical manifestation. This is a case report of a 27-year-old woman with a prior history of psychogenic non-epileptic attacks, intracranial hypertension, headache, visual impairment, papilloedema, and a BMI of 24 kg/m2. Upon acetazolamide treatment for intracranial hypertension and before the diagnosis of SLE was reached, the patient developed respiratory distress and metabolic acidosis, due to underlying SLE glomerulonephritis.

Bidragets oversatte titelIntracranial hypertension secondary to systemic lupus erythematosus
OriginalsprogDansk
ArtikelnummerV10200782
TidsskriftUgeskrift for læger [online]
Vol/bind183
Udgave nummer5
Sider (fra-til)1-3
Antal sider3
ISSN1603-6824
StatusUdgivet - 1 feb. 2021

Emneord

  • Adult
  • Female
  • Headache/etiology
  • Humans
  • Intracranial Hypertension/etiology
  • Lupus Erythematosus, Systemic/complications
  • Lupus Nephritis
  • Papilledema

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