Doyle James J, Hashimie Yasmeen, Metting Austin
Department of Internal Medicine, Baylor Scott & White Medical Center - Temple, Temple, Texas.
Department of Hematology-Oncology, Baylor Scott & White Medical Center - Temple, Temple, Texas.
Proc (Bayl Univ Med Cent). 2021 Jul 21;34(6):724-725. doi: 10.1080/08998280.2021.1953878. eCollection 2021.
Olfactory neuroblastomas are rare malignancies of the nasal and sinus cavities. They have been associated with paraneoplastic syndromes due to secretion of adrenocorticotropin hormone (ACTH) or antidiuretic hormone. These associated paraneoplastic syndromes can present with a wide variety of symptoms that can make diagnosis of the underlying tumor difficult. Here we present the case of a 23-year-old woman who had a seizure due to the development of posterior reversible leukoencephalopathy syndrome because of secondary hypertension due to Cushing's syndrome, which was in turn found to be due to ectopic ACTH production from a metastatic olfactory neuroblastoma.
嗅神经母细胞瘤是鼻腔和鼻窦罕见的恶性肿瘤。它们因分泌促肾上腺皮质激素(ACTH)或抗利尿激素而与副肿瘤综合征相关。这些相关的副肿瘤综合征可表现出各种各样的症状,这可能使潜在肿瘤的诊断变得困难。在此,我们报告一例23岁女性病例,该患者因库欣综合征继发高血压导致后部可逆性白质脑病综合征而发生癫痫发作,而库欣综合征又是由转移性嗅神经母细胞瘤异位分泌ACTH所致。