Rai Harpreet K, Reddy Kalpana
Internal Medicine, Northwell Health Long Island Jewish Forest Hills Hospital, Forest Hills, USA.
Endocrinology, Northwell Health Long Island Jewish Forest Hills Hospital, Forest Hills, USA.
Cureus. 2021 May 24;13(5):e15218. doi: 10.7759/cureus.15218.
Pheochromocytoma is a tumor arising from chromaffin cells of the medulla of adrenal gland and secretes excessive amounts of catecholamines: epinephrine and norepinephrine. It can also arise from sympathetic ganglia when it is referred to as catecholamine-secreting paragangliomas or extra-adrenal pheochromocytoma. Pheochromocytoma has been referred to as "the masquerader" for its numerous atypical presentations, which makes its diagnosis medically challenging. Here, we present a case of a 66-year-old female, presenting with high-grade fever for two weeks associated with generalized body aches. She had an extensive infectious, rheumatological and hematological workup. Ultimately, she was diagnosed with pheochromocytoma. After adrenalectomy, her fever and body ache resolved.
嗜铬细胞瘤是一种起源于肾上腺髓质嗜铬细胞的肿瘤,可分泌过量的儿茶酚胺:肾上腺素和去甲肾上腺素。当它起源于交感神经节时,被称为分泌儿茶酚胺的副神经节瘤或肾上腺外嗜铬细胞瘤。嗜铬细胞瘤因其众多非典型表现而被称为“伪装者”,这使其诊断在医学上具有挑战性。在此,我们报告一例66岁女性病例,该患者出现两周的高热并伴有全身疼痛。她接受了广泛的感染性、风湿性和血液学检查。最终,她被诊断为嗜铬细胞瘤。肾上腺切除术后,她的发热和身体疼痛症状消失。