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CASE REPORT
Bilateral adrenal haemorrhagic infarction in a patient with antiphospholipid syndrome
  1. Rebecca Louise Godfrey1,
  2. James Clark2,
  3. Benjamin Field2
  1. 1Frimley Health NHS Foundation Trust, Frimley, UK
  2. 2Surrey & Sussex Healthcare NHS Trust, Redhill, UK
  1. Correspondence to Dr Rebecca Louise Godfrey, r.godfrey1{at}uni.bsms.ac.uk

Summary

A 68-year-old woman with antiphospholipid syndrome presented with a 3-day history of bilateral loin pain, vomiting, fever and confusion. On examination she was febrile, hypotensive and tachycardic. Investigations revealed raised inflammatory markers, renal impairment and hyponatraemia. Abdominal ultrasound revealed two well-defined heterogeneous areas bilaterally in the region of the adrenal glands. This prompted serum cortisol measurement and a CT of the abdomen. Cortisol was low in the context of sepsis at 48 nmol/L, and CT confirmed bilateral heterogeneous adrenal pathology. The patient was managed for septic shock and adrenal insufficiency. She was recognised to have several risk factors for haemorrhagic infarction of the adrenals: antiphospholipid syndrome, sepsis, postoperative state and anticoagulant therapy. She was discharged well on glucocorticoid and mineralocorticoid therapy and a repeat CT at 4 weeks confirmed the diagnosis of bilateral adrenal infarct and haemorrhage.

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