Acute intermittent porphyria: Difference between revisions

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== Definition ==
+
== Background ==
   
  +
===Definition===
* Autosomal dominant mutation in HMB synthase with variable penetrance causing intermittent attacks characterized by neurovisceral symptoms
 
   
 
*Autosomal dominant mutation in HMB synthase with variable penetrance causing intermittent attacks characterized by neurovisceral symptoms
== Etiology ==
 
   
 
===Etiology===
* Defect in heme synthesis; specifically, in HMB synthase (hydroxymethylbilane synthase; porphobilinogen deaminase), which causes build-up of porphobilinogen
 
   
 
*Defect in heme synthesis; specifically, in HMB synthase (hydroxymethylbilane synthase; porphobilinogen deaminase), which causes build-up of porphobilinogen
== Clinical Presentation ==
 
   
 
==Clinical Manifestations==
=== History ===
 
   
* Prodromal symptoms, including restlessness
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*Prodromal symptoms, including restlessness
* Neurovisceral symptoms, including abdominal pain, tachycardia, constipation, psychosis, seizures, paralysis
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*Neurovisceral symptoms, including abdominal pain, tachycardia, constipation, psychosis, seizures, paralysis
 
*Red-brown urine
   
 
==Investigations==
=== Signs & Symptoms ===
 
   
 
*Electrolytes: may show hyponatremia or other abnormalities
* Red-brown urine
 
 
*'''Urine porphyrins (PBG)'''
   
 
==Management==
== Investigations ==
 
   
  +
===Acute===
* Electrolytes: may show hyponatremia or other abnormalities
 
* '''Urine porphyrins (PBG)'''
 
   
 
*Stop offending medication, start high carbohydrate diet
== Management ==
 
 
*Sometimes [[hematin]]
 
*If seizures: [[gabapentin]] or [[levetiracetam]]
   
=== Acute ===
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===Chronic===
   
 
*Avoid triggers, including [http://porphyriadrugs.com/ drugs]
* Stop offending medication, start high carb diet
 
 
*High-carbohydrate diet
* Sometimes hematin
 
 
*Screen for [[cirrhosis]] and [[hepatocellular carcinoma]]
* If seizures: gabapentin or levitiracetam
 
 
=== Chronic ===
 
 
* Avoid triggers, including drugs
 
* High-carb diet
 
* Screen for cirrhosis and hepatocellular carcinoma
 
   
 
[[Category:Hematology]]
 
[[Category:Hematology]]

Latest revision as of 08:27, 2 August 2020

Background

Definition

  • Autosomal dominant mutation in HMB synthase with variable penetrance causing intermittent attacks characterized by neurovisceral symptoms

Etiology

  • Defect in heme synthesis; specifically, in HMB synthase (hydroxymethylbilane synthase; porphobilinogen deaminase), which causes build-up of porphobilinogen

Clinical Manifestations

  • Prodromal symptoms, including restlessness
  • Neurovisceral symptoms, including abdominal pain, tachycardia, constipation, psychosis, seizures, paralysis
  • Red-brown urine

Investigations

  • Electrolytes: may show hyponatremia or other abnormalities
  • Urine porphyrins (PBG)

Management

Acute

Chronic