AI Article Synopsis

  • Adrenal necrosis during pregnancy is a rare but serious condition that can cause severe abdominal pain due to blood clots, often leading to delayed diagnosis and treatment.
  • The study aimed to identify specific clinical and paraclinical signs of adrenal necrosis to improve diagnostic timing and establish a management protocol involving a multidisciplinary approach.
  • Eight case studies of pregnant women diagnosed with adrenal necrosis via CT scans were analyzed, revealing common symptoms, and treatment involving anticoagulation for three to six months is recommended, along with assessments for potential adrenal insufficiency.

Article Abstract

Adrenal necrosis is a rare but serious cause of abdominal pain of thrombotic origin during pregnancy. There is often a delay in diagnosis and treatment. The objective was to specify the clinical and paraclinical signs suggestive of adrenal necrosis, making it possible to improve the delay in diagnostic. The secondary objective was to establish a multidisciplinary protocol regarding management. This is a case report of pregnant women with a radiological diagnosis of adrenal gland necrosis. In parallel, we carried out a systematic review in the same period. We studied these patients' clinical, biological and radiological data. We included eight patients with a computed tomography scan diagnosis of adrenal necrosis and fifteen articles in the literature describing twenty-four cases. All the patients presented with the same symptoms. The treatment was based on curative anticoagulation. The diagnosis of adrenal gland necrosis is worth suggesting in view of the array of sudden morphine-resistant abdominal pain associated with a biological inflammatory syndrome. The diagnosis is based on the computed tomography scan. Three to six months of curative anticoagulation is recommended as well as a thrombophilia and endocrinological assessment to rule out adrenal insufficiency.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531684PMC
http://dx.doi.org/10.3390/jcm12186036DOI Listing

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