Literature DB >> 22689598

Reversible steatohepatosis in a young boy with brittle type 1 diabetes mellitus: mauriac syndrome.

Makardhwaj Sarvadaman Shrivastava1, Atul Vijay Palkar, Namita J Padwal, Nivedita Moulick.   

Abstract

A 14-year-old male, diagnosed case of type 1 diabetes mellitus since 1 year, presented with uncontrolled blood glucose levels, non-compliance with insulin therapy and recurrent admissions with diabetic ketoacidosis. His blood glucose levels were difficult to control with wide fluctuations in insulin requirement. He had absent secondary sexual characteristics and hepatomegaly. Liver biopsy showed macrovesicularsteatosis without fibrosis or inflammation. Many glycogenated nuclei were present. He was started on intensive insulin therapy, whereby he showed subsequent regression of hepatomegaly and onset of pubertal spurt.

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Year:  2011        PMID: 22689598      PMCID: PMC3143339          DOI: 10.1136/bcr.03.2011.3975

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  3 in total

Review 1.  Mauriac syndrome: growth failure and type 1 diabetes mellitus.

Authors:  Mimi S Kim; J B Quintos
Journal:  Pediatr Endocrinol Rev       Date:  2008-08

2.  Bioptical liver changes in Mauriac syndrome.

Authors:  G Lorenz
Journal:  Zentralbl Allg Pathol       Date:  1981

3.  Mauriac syndrome in a 3-year-old boy.

Authors:  Shefali Mahesh; Robert J Karp; Salvador Castells; Jose Bernardo Q Quintos
Journal:  Endocr Pract       Date:  2007 Jan-Feb       Impact factor: 3.443

  3 in total
  2 in total

1.  Re-emergence of a rare syndrome: A case of mauriac syndrome.

Authors:  Manish Gutch; Rajeev Philip; Sanjay Saran; Rajiv Tyagi; Keshav Kumar Gupta
Journal:  Indian J Endocrinol Metab       Date:  2013-10

2.  Reversible severe glycogenic hepatopathy in type 1 diabetes.

Authors:  Jan de Laffolie; Clemens Kamrath; Diana Burchert; Claudia Böttcher; Stefan Alexander Wudy; Klaus-Peter Zimmer
Journal:  Wien Med Wochenschr       Date:  2021-01-20
  2 in total

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