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Vanishing Of Ruptured Adrenal Mass With Takotsubo Cardiomyopathy

Takeshita, Y. 2018Adrenal tumor

Takeshita, Y., Teramura, C., & Takamura, T. (2018). Vanishing of ruptured adrenal mass with takotsubo cardiomyopathy. Endocrine journal, 65(12), 1155–1159. https://doi.org/10.1507/endocrj.EJ18-0119

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Abstract

A 45-year-old male suddenly experienced left-flank abdominal pain. Echocardiography revealed akinesis of the 'takotsubo cardiomyopathy' type. He experienced a sudden haemodynamic collapse (blood pressure, 324/154 mmHg; pulse rate, 180 beats/min) during emergency cardiac catheterisation. An abdominal computed tomography (CT) revealed expansion of a soft tissue mass 64 × 33 mm in dimension in the left adrenal region, with accumulation of fluid surrounding the left pararenal space. Three days after the attack, his urinary catecholamine concentrations were slightly elevated. We suspected the patient as having a pheochromocytoma followed by acute haemorrhagic rupture, based on signatures of adrenal mass, 'takotsubo cardiomyopathy', and the hypertensive crisis. Over the next few weeks, he recovered well as an outpatient, and his blood pressure remained around 110/60 mmHg without medication. Three weeks after the attack, an abdominal CT showed shrinkage of the ruptured adrenal mass (to a diameter of 30 mm) and absorption of the retroperitoneal hematoma. On day 190 after the attack, abdominal CT did not detect any left adrenal mass. This is the first report of the case showing a complete vanishing of ruptured adrenal mass with takotsubo cardiomyopathy. Although surgical approaches for ruptured adrenal mass involve either emergency or elective surgery, the patients did not need even the elective surgery. Accumulation of the similar cases may unravel clinical factors predicting self-limiting of the ruptured adrenal mass to avoid unnecessary risky surgery.

Case Details

Disease Location

Adrenal gland

Personal Characteristics

45-year-old japanese male

Clinical Characteristics

Left-flank abdominal pain. Ecg demonstrated a 2-mm st-segment depression in the precordial leads, chest x-ray findings indicated a cardiothoracic ratio of 50%. Laboratory findings showed mild leukocytosis and elevated levels of myocardial enzymes (creatinine-kinase, troponin t, aspartate aminotransferase, lactate dehydrogenase), echocardiography revealed the apical areas with akinesis of the ‘takotsubo cardiomyopathy’ type. He was tentatively diagnosed with acute coronary syndrome and admitted to icu. During emergency cardiac catheterization, he experienced a sudden hemodynamic collapse (bp 324/154 mmhg and pr 180 beats/min). Treatment with antihypertension agents and nitroglycerin was initiated with non-invasive positive pressure ventilation. Abdominal CT revealed expansion of a soft tissue mass 64 × 33 mm in dimension in the left adrenal region, with accumulation of fluid surrounding the left pararenal space. Suspected a pheochromocytoma followed by acute haemorrhagic rupture, based on signatures of adrenal mass, ‘takotsubo cardiomyopathy’, and the hypertensive crisis

Remission Characteristics

Three weeks after the attack, an abdominal CT showed shrinkage of the ruptured adrenal mass and absorption of the retroperitoneal hematoma. MRI showed 30 mm- diameter left adrenal mass highly intense in t1- and moderately intense in t2-weighted images, which seems compatible findings with post-hemorrhagic state. PET did not reveal label accumulation, suggestive of coagulation necrosis of the mass. On day 190 after the attack, abdominal CT did not detect any left adrenal mass

Treatment & Mechanisms

Clinical Treatment

Cardiac catheterization