SEARCH WITHIN CONTENT
VOLUME 24 , ISSUE 8 ( August, 2020 ) > List of Articles
Sarala Kumari Daram, Murthy NLN Arumilli, L Siva Kumar Reddy, Duvvuru Nageshwar Reddy, Revanth Motor
Keywords : Acute intermittent porphyria, Porphyria, Posterior reversible encephalopathy syndrome
Citation Information : Daram SK, Arumilli MN, Reddy LS, Reddy DN, Motor R. Acute Intermittent Porphyria Presenting with Posterior Reversible Encephalopathy Syndrome: A Rare Cause of Abdominal Pain and Seizures. Indian J Crit Care Med 2020; 24 (8):724-726.
License: CC BY-NC 4.0
Published Online: 21-09-2020
Copyright Statement: Copyright © 2020; Jaypee Brothers Medical Publishers (P) Ltd.
Acute intermittent porphyria (AIP) is an acute neurovisceral porphyria caused due to inherited deficiency of porphobilinogen deaminase (also called hydroxymethylbilane synthase) (HMBS) in the heme biosynthesis pathway. AIP is rarely associated with posterior reversible encephalopathy syndrome (PRES), which is a clinicoradiological condition caused by the failure of the posterior circulation to autoregulate, resulting in cerebral edema, headaches, nausea, and seizures. AIP should be considered when a patient presents with unexplained abdominal pain and seizures. This association is important because drugs used in the management of seizures may worsen an attack of AIP. This case report describes a young woman who presented with AIP and PRES with seizures.
© Jaypee Brothers Medical Publishers (P) LTD.