Unilateral nonhaemorrhagic adrenal infarction as a cause of abdominal pain during pregnancy

Abstract Adrenal infarction is usually associated with bilateral adrenal hemorrhage in the setting of antiphospholipid syndrome or hemodynamic variation. Few cases of unilateral nonhemorrhagic adrenal infarction (NHAI) have been described in the literature. Here, we report a case occurring during pregnancy. A 30-year-old woman presented at 32 weeks of gestation with sudden-onset right abdominal pain and contractions. Unilateral adrenal infarction was diagnosed following computed tomography (CT). It showed an enlarged right adrenal, without hyperenhancement. Because of persisting contractions, despite medical care, she delivered a healthy, albeit premature, girl. Abdominal pain decreased right after delivery. Three month later, CT imaging showed atrophy of the right adrenal and a normal left adrenal. The patient’s adrenal hormonal function was normal. Accurate diagnosis of NHAI remains difficult as its clinical presentation is not specific. It can only be performed with adrenal imaging. Magnetic resonance imaging shows diffuse enlargement of one or both adrenals and an edema on T2-weighted images. Anticoagulation therapy may be discussed. Patients should be evaluated between 3 and 6 months after the event to assess adrenal size and function. In summary, NHAI during pregnancy is probably underdiagnosed and obstetricians should be aware of this or diagnostic difficulty.

[1]  S. Tatli,et al.  Acute Nonhemorrhagic Adrenal Infarction in Pregnancy: 10-Year MRI Incidence and Patient Outcomes at a Single Institution. , 2018, AJR. American journal of roentgenology.

[2]  K. Aljenaee,et al.  Unilateral adrenal infarction in pregnancy secondary to elevated factor VIII , 2017, Saudi medical journal.

[3]  Dean Malik,et al.  Non-haemorrhagic, bilateral adrenal infarction in a patient with antiphospholipid syndrome along with lupus myocarditis , 2016, BMJ Case Reports.

[4]  N. Matikainen,et al.  Adrenal infarction in a healthy pregnant woman , 2016, Obstetric medicine.

[5]  A. Samueloff,et al.  Non-hemorrhagic adrenal infarct in pregnancy - a rare clinical condition diagnosed by non-contrast magnetic resonance image. , 2016, European Journal of Obstetrics, Gynecology, and Reproductive Biology.

[6]  S. Tatli,et al.  Nonhemorrhagic Adrenal Infarction With Magnetic Resonance Imaging Features During Pregnancy , 2015, Obstetrics and gynecology.

[7]  G. Angelelli,et al.  Value of the CT “capsular sign” as a potential indicator of acute adrenal ischemia , 2015, Emergency Radiology.

[8]  Tony T Lee,et al.  Unilateral adrenal infarction in pregnancy , 2013, BMJ Case Reports.

[9]  O. Rawley,et al.  Elevated factor VIII levels and risk of venous thrombosis , 2012, British journal of haematology.

[10]  O. Dupuis,et al.  Ischémie aiguë unilatérale de la glande surrénale en cours du 3e trimestre de grossesse : à propos de deux cas , 2011 .

[11]  O. Dupuis,et al.  [Unilateral adrenal ischemia during third trimester of pregnancy: about two cases]. , 2011, Gynécologie Obstétrique & Fertilité.

[12]  O. Dupuis,et al.  Thrombose veineuse surrénalienne en cours de grossesse , 2010 .

[13]  A. James Pregnancy-associated thrombosis. , 2009, Hematology. American Society of Hematology. Education Program.

[14]  M. Dommergues,et al.  Nécrose des surrénales maternelles au troisième trimestre de la grossesse dans le cadre d’un syndrome des antiphospholipides : à propos d’un cas , 2008 .

[15]  M. Dommergues,et al.  [Maternal adrenal necrosis in the third trimester of pregnancy: a rare complication of antiphospholipid syndrome]. , 2008, Gynécologie Obstétrique & Fertilité.

[16]  A. Riddell,et al.  Sequential adrenal infarction without MRI-detectable hemorrhage in primary antiphospholipid-antibody syndrome. , 2004, AJR. American journal of roentgenology.

[17]  K. Bremme Haemostatic changes in pregnancy. , 2003, Best practice & research. Clinical haematology.

[18]  J. Piette,et al.  Adrenal Involvement in the Antiphospholipid Syndrome: Clinical and Immunologic Characteristics of 86 Patients , 2003, Medicine.

[19]  M. Sanak,et al.  Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease , 2002, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

[20]  J. Morris,et al.  Adrenal hemorrhage: a 25-year experience at the Mayo Clinic. , 2001, Mayo Clinic proceedings.

[21]  F. Gabreëls,et al.  A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? , 1998, American journal of human genetics.

[22]  T. Okai,et al.  Influence of compression of the inferior vena cava in the late second trimester on uterine and umbilical artery blood flow , 1996, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

[23]  R. Rao,et al.  Bilateral massive adrenal hemorrhage. , 1995, The Medical clinics of North America.

[24]  B. Fox,et al.  Venous infarction of the adrenal glands , 1976, The Journal of pathology.