Antosz-Popiołek Katarzyna, Koga-Batko Joanna, Suchecki Wojciech, Stopa Małgorzata, Zawadzka Katarzyna, Hajac Łukasz, Bolanowski Marek, Jawiarczyk-Przybyłowska Aleksandra
Student Scientific Group of Endocrinology, Wroclaw Medical University, Wybrzeże Pasteura 4, 50-367 Wroclaw, Poland.
Department and Clinic of Endocrinology and Internal Medicine, Wroclaw Medical University, Wybrzeże Pasteura 4, 50-367 Wroclaw, Poland.
J Clin Med. 2025 Jun 6;14(12):4028. doi: 10.3390/jcm14124028.
In this article, we present a case of a 49-year-old woman presenting with a recurrent metastatic neuroendocrine tumor. : Insulinomas are neuroendocrine tumors derived from beta cells of the pancreas that secrete insulin. Usually, they are benign tumors; however, metastatic insulinomas are an extremely rare malignant form of these tumors, carrying a significantly worse prognosis. : A 49-year-old woman, a patient in the University Hospital in Wroclaw in the Department of Endocrinology, Diabetes and Isotope Therapy, first presented with abdominal pain in 2009, when ultrasound and further examination led to the diagnosis of a tumor in the pancreas (a solid pseudopapillary tumor of the pancreas-meta NET G2), and the patient underwent distal pancreatectomy with splenectomy. For ten years, she was under observation, and her symptoms, such as abdominal pain, nausea, weight loss, and general weakness, reappeared in 2019. Then, magnetic resonance imaging (MRI) showed a lesion in the liver, and further histopathology revealed neuroendocrine tumor (NET) metastasis to the liver. In 2022, the patient presented with loss of consciousness and convulsion, loss of weight, and hypoglycemia after meals. In April 2022, the daily glycemic profile was recorded and a 72 h fasting test was performed; however, their results excluded insulinoma. Positron emission tomography-computed tomography (PET-CT) with 18F-fluorodeoxyglucose (18F-FDG) and PET with gallium-68-DOTA-(Tyr3)-octreotate (68Ga-DOTA-TATE) showed a metastatic proliferative process in the liver. Persistent hypoglycemia led to another hospitalization in May 2022, and repeated tests allowed for the diagnosis of insulinoma. Treatment with somatostatin analogs and diazoxide was started. A CT scan in November 2022 and a PET scan in January 2023 showed new metastases to the liver, bones, and cervical lymph nodes, and it was decided to intensify the treatment. In May 2023, the patient was qualified for Lutathera treatment for insulinoma at the University Clinical Hospital in Poznań. In June 2023, another disturbing symptom was reported by the patient, a painful lump in the breast. During diagnostics, metastases with high proliferation markers were found in both breasts. Two months later, in August 2023, the patient received another dose of Lutathera. In October 2023, significant progression of liver lesions, metastases to bones of the spine, ribs, and pelvis, and periaortic and pelvic lymphadenopathy were found as well as elevated values of neuron-specific enolase and calcitonin. The patient was also referred to the Palliative Medicine Home Hospice. In consultation with the Lower Silesian Cancer Center, the decision was made to forgo further treatment with PRRT and initiate systemic chemotherapy. Despite the chosen treatment, the patient died on 27/DEC/2023. : This case report can serve clinicians, as it presents a case of an extremely rare and insidious tumor, metastatic insulinoma.
在本文中,我们报告了一例49岁女性复发性转移性神经内分泌肿瘤的病例。胰岛素瘤是起源于胰腺β细胞并分泌胰岛素的神经内分泌肿瘤。通常,它们是良性肿瘤;然而,转移性胰岛素瘤是这些肿瘤中极其罕见的恶性形式,预后明显更差。一名49岁女性,是弗罗茨瓦夫大学医院内分泌、糖尿病和同位素治疗科的患者,2009年首次出现腹痛,当时超声检查及进一步检查诊断为胰腺肿瘤(胰腺实性假乳头状肿瘤-转移性腺神经内分泌肿瘤G2),患者接受了胰体尾切除术加脾切除术。十年来,她一直处于观察中,2019年,她的腹痛、恶心、体重减轻和全身乏力等症状再次出现。随后,磁共振成像(MRI)显示肝脏有病变,进一步的组织病理学检查显示神经内分泌肿瘤(NET)转移至肝脏。2022年,患者出现意识丧失、抽搐、体重减轻和餐后低血糖。2022年4月,记录了每日血糖谱并进行了72小时禁食试验;然而,结果排除了胰岛素瘤。18F-氟脱氧葡萄糖(18F-FDG)正电子发射断层扫描-计算机断层扫描(PET-CT)和镓-68-DOTA-(Tyr3)-奥曲肽(68Ga-DOTA-TATE)PET显示肝脏有转移性增殖过程。持续性低血糖导致患者于2022年5月再次住院,重复检查后诊断为胰岛素瘤。开始使用生长抑素类似物和二氮嗪进行治疗。2022年11月的CT扫描和2023年1月的PET扫描显示肝脏、骨骼和颈部淋巴结出现新的转移灶,决定加强治疗。2023年5月,患者在波兹南大学临床医院符合接受镥-177奥曲肽治疗胰岛素瘤的条件。2023年6月,患者报告了另一个令人不安的症状,乳房出现疼痛性肿块。在诊断过程中,发现双侧乳房有高增殖标志物的转移灶。两个月后,即2023年8月,患者接受了另一剂镥-177奥曲肽。2023年10月,发现肝脏病变显著进展,脊柱、肋骨和骨盆骨转移,腹主动脉旁和盆腔淋巴结肿大,以及神经元特异性烯醇化酶和降钙素值升高。患者还被转诊至姑息医学家庭临终关怀机构。经与下西里西亚癌症中心协商,决定放弃进一步的肽受体放射性核素治疗(PRRT)并开始全身化疗。尽管采取了所选的治疗方法,患者仍于2023年12月27日死亡。本病例报告可为临床医生提供参考,因为它呈现了一例极其罕见且隐匿的肿瘤——转移性胰岛素瘤的病例。