Acute fatty liver during pregnancy and gestational diabetes insipidus: a case report

lap. Imaging findings, such as on abdominal ultrasound, computed tomography, and magnetic resonance imaging, may support the diagnosis, but such images are not required for the diagnosis [2]. A liver ultrasound may show non-specific changes, including fatty infiltration or brightness. Although a liver biopsy can make a definite diagnosis of AFLP, it is too invasive to be routinely performed [2, 5]. Early diagnosis and treatment decreased the risk of life-threatening consequences for the mother and fetus. Prompt delivery is thought to effectively improve prognosis [1, 5]. Another complication of pregnancy is GDI, which is characterized by polydipsia and hypotonic polyuria. GDI has an incidence of approximately four cases for every 100,000 pregnancies [6]. It is thought to be caused by decreased AVP levels secondary to excessive vasopressinase activity [7]. Vasopressinase is a placental enzyme that degrades both AVP and oxytocin [6] but not deamino-Cys 1,D-arg 8-vasopressin (dDAVP) [8], which is a synthetic form of endogenous AVP with a different N-terminal. Although AVP levels increase during pregnancy to maintain sufficient antidiuretic activity, vasopressinase levels from the placenta may increase as well, thereby resulting in a decreased renal effect; this increase is the main cause of subclinical diabetes insipidus [6]. However, in pregnant women with impaired liver function (such as AFLP, Acute fatty liver during pregnancy and gestational diabetes insipidus: a case report

[1]  J. Wolf,et al.  Acute Fatty Liver Disease of Pregnancy: Updates in Pathogenesis, Diagnosis, and Management , 2017, The American Journal of Gastroenterology.

[2]  Joseph C. Ahn,et al.  ACG Clinical Guideline: Liver Disease and Pregnancy , 2016, The American Journal of Gastroenterology.

[3]  Jinlai Meng,et al.  Prenatal predictors in postpartum recovery for acute fatty liver of pregnancy: experiences at a tertiary referral center , 2016, Archives of Gynecology and Obstetrics.

[4]  A. Goel,et al.  How accurate are the Swansea criteria to diagnose acute fatty liver of pregnancy in predicting hepatic microvesicular steatosis? , 2010, Gut.

[5]  P. Brocklehurst,et al.  A prospective national study of acute fatty liver of pregnancy in the UK , 2008, Gut.

[6]  F. Gungor,et al.  Transient gestational diabetes insipidus diagnosed in successive pregnancies: review of pathophysiology, diagnosis, treatment, and management of delivery , 2007, Pituitary.

[7]  J. Ray DDAVP use during pregnancy: an analysis of its safety for mother and child. , 1998, Obstetrical & gynecological survey.

[8]  M. Lindheimer,et al.  Diagnosis and management of diabetes insipidus during pregnancy. , 1996, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

[9]  A. Seymour,et al.  Transient diabetes insipidus and acute fatty liver of pregnancy , 1994, British journal of obstetrics and gynaecology.

[10]  Y. Oiso,et al.  Aggravation of subclinical diabetes insipidus during pregnancy , 1992, The New England journal of medicine.

[11]  J. Davison,et al.  Idiopathic acute fatty liver of pregnancy associated with transient diabetes insipidus. Case report , 1987, British journal of obstetrics and gynaecology.

[12]  B. Velkeniers,et al.  Idiopathic acute fatty liver of pregnancy associated with transient diabetes insipidus , 1987 .