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Síndrome de Mauriac: reporte de un caso.

Authors :
Eduardo Pérez-Laínez, Sergio
Rueda-Ochoa, Hugo
Deraz-Cabral, Sergio
Simental-Mendía, Luis E.
Source :
Acta Pediatrica de Mexico. nov/dec2018, Vol. 39 Issue 6, p349-354. 6p. 1 Color Photograph, 2 Black and White Photographs, 1 Diagram, 1 Chart.
Publication Year :
2018

Abstract

INTRODUCTION: Mauriac syndrome is an uncommon condition characterized by growth retardation, hepatomegaly and obesity in children with type 1 diabetes. CASE REPORT: We describe an 11 years old female patient with type 1 diabetes of 8 years duration treated with glargine and rapid-acting insulin. She presented gradually increased abdominal volume of approximately 3 months duration and poor glycemic control over 6 months. In addition, she exhibited polydipsia and polyuria. Physical examination revealed growth retardation, pubertal delay and hepatomegaly. Markers of viral or autoimmune hepatitis were negatives. Finally, liver biopsy reported abundant glycogen deposition. CONCLUSION: Although the Mauriac syndrome is an unusual condition, it should be suspected in patients with uncontrolled type 1 diabetes in order to establish a timely diagnosis and treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
Spanish
ISSN :
01862391
Volume :
39
Issue :
6
Database :
Academic Search Index
Journal :
Acta Pediatrica de Mexico
Publication Type :
Academic Journal
Accession number :
133730486
Full Text :
https://doi.org/10.18233/APM39No6pp349-3541732