Khan Samiha, Fayyaz Beenish, Patel Janki
Greater Baltimore Medical Center, Towson, MD, USA.
J Community Hosp Intern Med Perspect. 2020 Jun 14;10(3):250-254. doi: 10.1080/20009666.2020.1767272.
Neurofibromatosis-1 (NF-1) is a genetic neuro-cutaneous disorder that is associated with an increased prevalence of pheochromocytoma (PHEO). However, this association may not be commonly anticipated by physicians, as patients may be normotensive. In addition, NF-1 patients can be asymptomatic and/or normotensive. These factors can result in a delayed or missed diagnosis of pheochromocytoma leading to catastrophic complications. Currently, it is recommended to perform annual blood pressure monitoring in patients with NF-1 and to test for pheochromocytoma only if found to be hypertensive. However, recent studies show that this practice may lead to underdiagnosis of pheochromocytoma. Therefore, suggesting routine biochemical testing for pheochromocytoma in all patients with NF-1. In this case report, we discuss the factors which can lead to a delayed diagnosis of pheochromocytoma in a patient with known NF-1 and hypertension.
神经纤维瘤病1型(NF-1)是一种遗传性神经皮肤疾病,与嗜铬细胞瘤(PHEO)的患病率增加有关。然而,由于患者可能血压正常,医生可能通常不会预期到这种关联。此外,NF-1患者可能无症状和/或血压正常。这些因素可能导致嗜铬细胞瘤的诊断延迟或漏诊,从而引发灾难性并发症。目前,建议对NF-1患者进行年度血压监测,只有在发现高血压时才检测嗜铬细胞瘤。然而,最近的研究表明,这种做法可能导致嗜铬细胞瘤诊断不足。因此,建议对所有NF-1患者进行嗜铬细胞瘤的常规生化检测。在本病例报告中,我们讨论了在已知患有NF-1和高血压的患者中可能导致嗜铬细胞瘤诊断延迟的因素。