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Tytuł pozycji:

A rare case of posterior reversible encephalopathy syndrome in a patient with severe leptospirosis complicated with rhabdomyolysis and acute kidney injury; a case report.

Tytuł:
A rare case of posterior reversible encephalopathy syndrome in a patient with severe leptospirosis complicated with rhabdomyolysis and acute kidney injury; a case report.
Autorzy:
Lakmali JPR; National Hospital of Sri Lanka, Colombo 08, Sri Lanka. .
Thirumavalavan K; National Hospital of Sri Lanka, Colombo 08, Sri Lanka.
Dissanayake D; National Hospital of Sri Lanka, Colombo 08, Sri Lanka.
Źródło:
BMC infectious diseases [BMC Infect Dis] 2021 Jun 03; Vol. 21 (1), pp. 522. Date of Electronic Publication: 2021 Jun 03.
Typ publikacji:
Case Reports; Journal Article
Język:
English
Imprint Name(s):
Original Publication: London : BioMed Central, [2001-
MeSH Terms:
Acute Kidney Injury/*complications
Leptospirosis/*complications
Posterior Leukoencephalopathy Syndrome/*etiology
Rhabdomyolysis/*complications
Acute Kidney Injury/diagnosis ; Acute Kidney Injury/physiopathology ; Acute Kidney Injury/therapy ; Brain/diagnostic imaging ; Diagnosis, Differential ; Humans ; Leptospirosis/diagnosis ; Leptospirosis/physiopathology ; Leptospirosis/therapy ; Magnetic Resonance Imaging ; Male ; Posterior Leukoencephalopathy Syndrome/diagnosis ; Posterior Leukoencephalopathy Syndrome/physiopathology ; Posterior Leukoencephalopathy Syndrome/therapy ; Rhabdomyolysis/diagnosis ; Rhabdomyolysis/physiopathology ; Rhabdomyolysis/therapy ; Treatment Outcome ; Young Adult
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Contributed Indexing:
Keywords: Acute kidney injury; Leptospirosis; Posterior reversible encephalopathy syndrome; Rhabdomyolysis
Entry Date(s):
Date Created: 20210604 Date Completed: 20210609 Latest Revision: 20210609
Update Code:
20240104
PubMed Central ID:
PMC8176595
DOI:
10.1186/s12879-021-06240-2
PMID:
34082705
Czasopismo naukowe
Background: Leptospirosis is a zoonotic spirochetal disease caused by Leptospira interrogans. The clinical presentation ranges from an asymptomatic state to a fatal multiorgan dysfunction. Neurological manifestations including aseptic meningitis, spinal cord and peripheral nerve involvement, cranial neuropathies and cerebellar syndrome are well recognized with varying frequencies among patients with this disease. Posterior reversible encephalopathy syndrome is a very rare occurrence in leptospirosis and only two cases are reported in the medical literature up to now. We report a case of posterior reversible encephalopathy syndrome in a patient with leptospirosis with rhabdomyolysis and acute kidney injury.
Case Presentation: A 21 year-old male presented with fever and oliguric acute kidney injury with rhabdomyolysis. A diagnosis of leptospirosis was made and he was being managed according to the standard practice together with regular hemodialysis. The clinical condition was improving gradually. On day 8 of the illness, he developed headache and sudden painless complete bilateral vision loss followed by several brief generalized tonic clonic seizure attacks. Examination was significant for a Glasgow Coma Scale of 14/15, blood pressure of 150/90 mmHg and complete bilateral blindness. The findings of magnetic resonance imaging of the brain were compatible with posterior reversible encephalopathy syndrome. He was managed with blood pressure control and antiepileptics with supportive measures and standard treatment for leptospirosis and made a complete recovery.
Conclusion: Posterior reversible encephalopathy syndrome, though very rare with leptospirosis, should be considered as a differential diagnosis in a patient with new onset visual symptoms and seizures, especially during the immune phase. Optimal supportive care together with careful blood pressure control and seizure management would yield a favourable outcome in this reversible entity.
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