Freeman S R M, Mitra S, Malik T H, Flanagan P, Selby P
Department of Otolaryngology, Manchester Royal Infirmary, Manchester, UK.
Rhinology. 2005 Mar;43(1):61-5.
Arginine vasopressin hormone-secreting olfactory neuroblastomas are extremely rare, with fewer than twenty cases reported in the literature. Two of these cases, both initially presenting with the syndrome of inappropriate antidiuretic hormone, are presented. The second tumour was successfully identified using somatostatin receptor (octreotide) radiographic scintography.
The pathological specimens from both cases were examined immunohistochemically for somatostatin receptors.
Samples from both cases demonstrated positivity for somatostatin receptors.
This report demonstrates the potential use of somatastatin analogues in the investigation, follow-up and treatment of patients with olfactory neuroblastoma.
分泌精氨酸加压素激素的嗅神经母细胞瘤极为罕见,文献报道不足20例。本文报告其中2例,均最初表现为抗利尿激素分泌异常综合征。第二例肿瘤通过生长抑素受体(奥曲肽)放射性闪烁扫描得以成功识别。
对两例病例的病理标本进行生长抑素受体免疫组化检查。
两例病例的标本均显示生长抑素受体呈阳性。
本报告证明生长抑素类似物在嗅神经母细胞瘤患者的检查、随访和治疗中具有潜在用途。