| Literature DB >> 22454794 |
Gaurav Jain1, Jeffrey I Bennett, David S Resch, John E Godwin.
Abstract
Acute porphyrias are often misdiagnosed and most commonly present as atypical neuropsychiatric symptoms or acute abdominal pain. Clinicians should suspect acute porphyrias in patients presenting with variable neuropsychiatric symptoms and unexplained pain. Proper identification can lead to less iatrogenicity associated with porphyrinogenic agents, appropriate management, and a better patient outcome. The case of a patient with hereditary coproporphyria, one of the acute porphyrias, is presented to illustrate the broad manifestations, unsuspected diagnosis, and difficulties in management.Entities:
Year: 2011 PMID: 22454794 PMCID: PMC3304676 DOI: 10.4088/PCC.11br01234
Source DB: PubMed Journal: Prim Care Companion CNS Disord ISSN: 2155-7780