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 titel | Intracranial hypertension secondary to systemic lupus erythematosus |
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Originalsprog | Dansk |
Artikelnummer | V10200782 |
Tidsskrift | Ugeskrift for læger [online] |
Vol/bind | 183 |
Udgave nummer | 5 |
Sider (fra-til) | 1-3 |
Antal sider | 3 |
ISSN | 1603-6824 |
Status | Udgivet - 1 feb. 2021 |
Emneord
- Adult
- Female
- Headache/etiology
- Humans
- Intracranial Hypertension/etiology
- Lupus Erythematosus, Systemic/complications
- Lupus Nephritis
- Papilledema