Universidad Autónoma de Nuevo Leon, Hospital Universitario "Dr. Jose Eleuterio Gonzalez" y Facultad de Medicina, Endocrinology Service, Monterrey Nuevo Leon, Mexico,
Universidad Autónoma de Nuevo Leon, Hospital Universitario "Dr. Jose Eleuterio Gonzalez" y Facultad de Medicina, Endocrinology Service, Monterrey Nuevo Leon, Mexico.
Arch Endocrinol Metab. 2021 Nov 24;65(6):852-857. doi: 10.20945/2359-3997000000342. Epub 2021 Mar 19.
Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors that result in the uncontrolled release of catecholamines and secondary hypertension. They usually manifest with episodic blood pressure fluctuations, headaches and palpitations. In some cases PPGLs may be asymptomatic until they are detected as a diagnostic approach to other diseases. There have been reports that have associated PPGLs with arterial thrombosis, some with the additional finding of intracardiac thrombi. We present the case of a 21-year-old male Hispanic patient with a recurrent para-aortic paraganglioma detected by persistent hypertension, bilateral lower limb artery thrombosis and an intracardiac thrombus.
嗜铬细胞瘤和副神经节瘤(PPGL)是罕见的神经内分泌肿瘤,导致儿茶酚胺的失控释放和继发性高血压。它们通常表现为间歇性血压波动、头痛和心悸。在某些情况下,PPGL 可能没有症状,直到它们作为其他疾病的诊断方法被发现。有报道称,PPGL 与动脉血栓形成有关,其中一些还伴有心内血栓形成。我们报告了一例 21 岁的西班牙裔男性患者,因持续性高血压、双侧下肢动脉血栓形成和心内血栓形成而反复出现腹主动脉旁副神经节瘤。