Wang Amber R, Dean Stephanie A, Grebe Stefan K, Hood Ian C
Hospital of the University of Pennsylvania - Department of Pathology.
Sparrow Forensic Pathology.
Acad Forensic Pathol. 2016 Jun;6(2):315-324. doi: 10.23907/2016.032. Epub 2016 Jun 1.
Pheochromocytomas and paragangliomas are catecholamine-secreting tumors characterized by excessive adrenergic stimulation. Common manifestations include hypertension, headache, sweating, and palpitations; however, rare life-threatening conditions have also been reported and include cardiovascular shock, myocardial infarction, arrhythmias, and cardiomyopathy. We report a case of a previously healthy 31-year-old postpartum female presenting with headache who died suddenly in an emergency room. Autopsy revealed a pheochromocytoma of the right adrenal with significantly elevated metanephrine concentrations and acute "myocarditis." Sudden excessive catecholamine release can cause cardiovascular complications and be rapidly fatal without significant elevation of blood pressure. Awareness of this association by the medical examiner/coroner is vital in order to properly classify the death and apprise relatives of the potential utility of genetic screening.
嗜铬细胞瘤和副神经节瘤是分泌儿茶酚胺的肿瘤,其特征为肾上腺素能刺激过度。常见表现包括高血压、头痛、出汗和心悸;然而,也有罕见的危及生命的情况被报道,包括心血管休克、心肌梗死、心律失常和心肌病。我们报告一例既往健康的31岁产后女性,因头痛就诊,在急诊室突然死亡。尸检发现右肾上腺嗜铬细胞瘤,甲氧基肾上腺素浓度显著升高,并有急性“心肌炎”。儿茶酚胺突然过度释放可导致心血管并发症,在血压无显著升高的情况下可迅速致命。法医/验尸官认识到这种关联对于正确分类死因并告知亲属基因筛查的潜在作用至关重要。