Background: An acute abdomen can have a variety of causes. A commonly missed cause of abdominal pain is direct substance abuse and its sequelae. The use of methamphetamine is rising in the United States resulting in significant morbidity and mortality. There has been no reported case of methamphetamine-induced adrenal infarction based on an extensive review of available literature.
Case Presentation: We present a case of a 34-year-old Hispanic man who presented with acute abdominal pain secondary to adrenal infarction in the setting of methamphetamine use. Left paraumbilical tenderness was present on abdominal examination. Contrast-enhanced CT of the abdomen and pelvis revealed internal hypoenhancement of the left adrenal gland, consistent with acute left adrenal infarction. The patient was managed with enoxaparin and apixaban.
Conclusion: Substance abuse, especially among young patients, can at times present with acute abdomen. This mandates physicians to be vigilant and take into consideration the history of substance abuse and relevant investigations. Timely diagnosis and management can prevent life-threatening complications.
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http://dx.doi.org/10.1186/s13256-022-03573-7 | DOI Listing |
J Cardiothorac Surg
December 2024
Zhejiang Taizhou Hospital, Taizhou, China.
Pheochromocytoma is rare in clinical practice, with patients typically presenting with headache, high blood pressure and sweating. Patients who develop a pheochromocytoma crisis are particularly rare. This report describes the case of a patient in a pheochromocytoma crisis who presented with severe cardiogenic shock, acute respiratory failure, and acute coronary syndrome.
View Article and Find Full Text PDFCureus
December 2024
Diabetes and Endocrinology, Peterborough City Hospital, Peterborough, GBR.
Pheochromocytoma is a rare neuroendocrine tumor that secretes excess catecholamines. Patients present with a classical triad of headache, palpitations, and sweating. If untreated, pheochromocytoma can result in life-threatening cardiovascular complications.
View Article and Find Full Text PDFBMJ Case Rep
December 2024
General Surgery, Gold Coast University Hospital, Southport, Queensland, Australia.
BMJ Case Rep
December 2024
Cardiology, Université de Fribourg Faculté de médecine, Fribourg, Switzerland
Phaeochromocytomas are rare catecholamine-secreting tumours, usually benign, originating from chromaffin cells of the adrenal glands. Their typical presentation includes the triad of headaches, sweating and tachycardia due to excessive catecholamine release. However, many patients do not exhibit all three symptoms, making diagnosis challenging.
View Article and Find Full Text PDFJ Endocr Soc
October 2024
Department of Cardiovascular Medicine, Baystate Medical Center, Springfield, MA 01199, USA.
Context: Patients with adrenal insufficiency (AI) have both increased risk of cardiovascular disease and adverse outcomes with many medical emergencies. However, limited data exist specifically regarding ST-segment elevation myocardial infarction (STEMI) in the context of AI.
Objective: To evaluate associations between AI and in-hospital outcomes of patients with STEMI.
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