Undiagnosed Pheochromocytoma Simulating Malignant Hyperthermia.
Nisha S Ramani1, Robert Stoppacher, Ajaykumar C Morani
1From the *SUNY Upstate Medical University, Syracuse, NY; and †The University of Texas MD Anderson Cancer Center, Houston, TX.
Summary
Pheochromocytoma, a rare tumor, can mimic malignant hyperthermia, leading to fatal outcomes if undiagnosed. Autopsy revealed a catecholamine-producing tumor as the cause of death, highlighting the need for vigilance.
Area of Science:
- Endocrinology
- Pathology
- Anesthesiology
Background:
- Pheochromocytomas are rare neuroendocrine tumors producing catecholamines.
- Early diagnosis is crucial as they are surgically curable but potentially lethal.
- This case highlights a patient misdiagnosed with malignant hyperthermia before autopsy confirmed pheochromocytoma.
Observation:
- A 53-year-old man developed severe hypertension, followed by a precipitous drop in blood pressure post-surgery.
- He exhibited high fever (42.2°C), rapid breathing, and ultimately died despite stabilization attempts.
- Autopsy revealed a large (10 cm) adrenal pheochromocytoma with high catecholamine levels (metanephrines/normetanephrine).
Findings:
- The patient's presentation mimicked malignant hyperthermia.
- The adrenal tumor was confirmed as the cause of death, complicated by general anesthesia.
- Elevated urinary catecholamine metabolites confirmed active pheochromocytoma.
Implications:
- Pheochromocytoma should be considered in the differential diagnosis of patients presenting with symptoms suggestive of malignant hyperthermia.
- Awareness among pathologists is essential when reviewing cases with a prior malignant hyperthermia diagnosis.
- Appropriate management of pheochromocytoma is critical to prevent fatal complications, especially during surgery.
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