Abdlkadir A S, Ruzzeh S, Al-Ibraheem A
"King Hussein" Cancer Center (KHCC) - Nuclear Medicine and PET/CT, Amman, Jordan.
The University of Jordan - School of Medicine, Amman, Jordan.
Acta Endocrinol (Buchar). 2024 Jul-Sep;20(3):388-392. doi: 10.4183/aeb.2024.388. Epub 2025 May 23.
We aim to describe a patient diagnosed with a rare and aggressive metastatic pattern of an ileal neuroendocrine tumor (NET). A 53-year-old male patient was referred to our cancer care center following the diagnosis of an ileal NET for further evaluation. As part of the initial diagnostic workup, 68Ga-DOTATOC positron emission tomography/computed tomography was conducted. The scan revealed a fulminant metastatic pattern of somatostatin-positive lesions affecting the axial and peripheral skeleton, liver, and a few lesions involving the brain leptomeninges and right extra-orbital eye muscle. Despite the prompt diagnosis and systematic therapeutic approach offered according to institutional guidelines, the patient did not achieve an optimal clinical response, resulting in his demise 18 months after his initial diagnosis. This case is shared with the primary aim of raising awareness of such an unreported aggressive metastatic pattern and encouraging further clinical investigations for patients with similar aggressive metastatic patterns to achieve optimal therapy and care.
我们旨在描述一名被诊断为具有罕见且侵袭性转移模式的回肠神经内分泌肿瘤(NET)患者。一名53岁男性患者在被诊断为回肠NET后被转诊至我们的癌症护理中心进行进一步评估。作为初始诊断检查的一部分,进行了68Ga-DOTATOC正电子发射断层扫描/计算机断层扫描。扫描显示生长抑素阳性病变呈暴发性转移模式,累及中轴和外周骨骼、肝脏,还有一些病变累及脑软脑膜和右眶外眼肌。尽管根据机构指南进行了及时诊断和系统治疗,但患者并未获得最佳临床反应,在初次诊断18个月后死亡。分享此病例的主要目的是提高对这种未报道的侵袭性转移模式的认识,并鼓励对具有类似侵袭性转移模式的患者进行进一步临床研究,以实现最佳治疗和护理。