Severe porphyric neuropathy – importance of screening for porphyria in Guillain-Barré syndrome

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dc.contributor.author Schutte, Clara-Maria
dc.contributor.author Van der Meyden, C.H. (Kees)
dc.contributor.author Van Niekerk, Linette
dc.contributor.author Kakaza, Mandisa
dc.contributor.author Van Coller, Riaan
dc.contributor.author Ueckermann, Veronica
dc.contributor.author Oosthuizen, Nicholette M.
dc.date.accessioned 2016-05-10T06:34:34Z
dc.date.available 2016-05-10T06:34:34Z
dc.date.issued 2016-01
dc.description.abstract The hepatic porphyrias are a group of rare metabolic disorders, each of which is associated with a specific enzymatic alteration in the haem biosynthesis pathway. In South Africa (SA), a high incidence of variegate porphyria (VP) is seen as a result of a founder effect, but acute intermittent porphyria (AIP) is also encountered. The development of acute neurovisceral attacks is related to environmental factors, including medications, hormones and diet. A possible manifestation of a severe attack is rapidly progressing quadriparesis, which may mimic Guillain- Barré syndrome. We present four such cases, highlighting that acute porphyria should be considered in the differential diagnosis of Guillain- Barré syndrome. Three patients presented to Steve Biko Academic Hospital, Pretoria, SA, with progressive quadriparesis, and one to a private hospital with acute abdominal pain followed by rapidly progressive quadriparesis. Two patients had started antiretroviral therapy before the development of symptoms, and one had started antituberculosis therapy. All patients had marked weakness with depressed reflexes, and showed varying degrees of confusion. An initial diagnosis of Guillain-Barré syndrome led to administration of intravenous immunoglobulins in two patients. On testing for porphyria, it was found that two patients had AIP and two VP. Electrophysiological investigations revealed severe mainly motor axonal neuropathy in all. Two patients deteriorated to the point of requiring mechanical ventilation, and one of them died due to complications of critical illness. Haemin was administered to three patients, but the process of obtaining this medication was slow, which delayed the recommended early administration. The surviving patients showed minimal recovery and remained severely disabled. Porphyric neuropathy should always be considered as a differential diagnosis in a patient with an acute neuropathy, especially in SA. Absence of abdominal pain does not exclude the possibility of porphyria, and attacks may be precipitated by antiretroviral and antituberculosis medication. The outcome of our patients was not favourable; specifically, obtaining haemin was a challenge in the state hospital setting. en_ZA
dc.description.department Chemical Pathology en_ZA
dc.description.department Internal Medicine en_ZA
dc.description.department Neurology en_ZA
dc.description.librarian am2016 en_ZA
dc.description.uri http://www.samj.org.za en_ZA
dc.identifier.citation Schutte, CM, Van der Meyden, CH, Van Niekerk, L, Kakaza, M, Van Coller, R, Ueckermann, V & Oosthuizen, NM 2015, 'Severe porphyric neuropathy – importance of screening for porphyria in Guillain-Barré syndrome', South African Medical Journal, vol. 106, no. 1, pp. 44-47. en_ZA
dc.identifier.issn 0256-9574 (print)
dc.identifier.issn 2078-5135 (online)
dc.identifier.other 10.7196/SAMJ.2016.v106i1.10118
dc.identifier.uri http://hdl.handle.net/2263/52548
dc.language.iso en en_ZA
dc.publisher Health and Medical Publishing Group en_ZA
dc.rights © 2016 Health & Medical Publishing Group. This work is licensed under a Creative Commons Attribution-NonCommercial Works License (CC BY-NC 3.0). en_ZA
dc.subject Guillain-Barré syndrome en_ZA
dc.subject Hepatic porphyrias en_ZA
dc.subject Patient en_ZA
dc.subject South Africa en_ZA
dc.subject South Africa (SA) en_ZA
dc.subject Variegate porphyria (VP) en_ZA
dc.subject Acute intermittent porphyria (AIP) en_ZA
dc.title Severe porphyric neuropathy – importance of screening for porphyria in Guillain-Barré syndrome en_ZA
dc.type Article en_ZA


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