A Rare Case of Persistent Lactic Acidosis in the ICU: Glycogenic Hepatopathy and Mauriac Syndrome

المؤلفون المشاركون

Deemer, Kirsten S.
Alvarez, George F.

المصدر

Case Reports in Critical Care

العدد

المجلد 2016، العدد 2016 (31 ديسمبر/كانون الأول 2016)، ص ص. 1-4، 4ص.

الناشر

Hindawi Publishing Corporation

تاريخ النشر

2016-07-25

دولة النشر

مصر

عدد الصفحات

4

التخصصات الرئيسية

الأمراض

الملخص EN

Mauriac syndrome is a rare disorder that can present with the single feature of glycogenic hepatopathy in children and adults with poorly controlled diabetes mellitus.

An often underrecognized finding of glycogenic hepatopathy is lactic acidosis and hyperlactatemia.

Primary treatment of glycogenic hepatopathy is improved long-term blood glucose control.

Resolution of symptoms and hepatomegaly will occur with improvement in hemoglobin A1C.

We present here a case of a young adult female presenting to the intensive care unit with Mauriac syndrome.

This case demonstrates exacerbation of lactic acidosis in a patient with glycogenic hepatopathy treated for diabetic ketoacidosis with high dose insulin and dextrose.

نمط استشهاد جمعية علماء النفس الأمريكية (APA)

Deemer, Kirsten S.& Alvarez, George F.. 2016. A Rare Case of Persistent Lactic Acidosis in the ICU: Glycogenic Hepatopathy and Mauriac Syndrome. Case Reports in Critical Care،Vol. 2016, no. 2016, pp.1-4.
https://search.emarefa.net/detail/BIM-1100443

نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)

Deemer, Kirsten S.& Alvarez, George F.. A Rare Case of Persistent Lactic Acidosis in the ICU: Glycogenic Hepatopathy and Mauriac Syndrome. Case Reports in Critical Care No. 2016 (2016), pp.1-4.
https://search.emarefa.net/detail/BIM-1100443

نمط استشهاد الجمعية الطبية الأمريكية (AMA)

Deemer, Kirsten S.& Alvarez, George F.. A Rare Case of Persistent Lactic Acidosis in the ICU: Glycogenic Hepatopathy and Mauriac Syndrome. Case Reports in Critical Care. 2016. Vol. 2016, no. 2016, pp.1-4.
https://search.emarefa.net/detail/BIM-1100443

نوع البيانات

مقالات

لغة النص

الإنجليزية

الملاحظات

Includes bibliographical references

رقم السجل

BIM-1100443