Milanetto Anna Caterina, Fassan Matteo, David Alina, Pasquali Claudio
Pancreatic and Endocrine Digestive Surgical Unit, Department of Surgery, Oncology and Gastroenterology, University of Padua, via Giustiniani, 2-35128 Padua, Italy.
Surgical Pathology Unit, Department of Medicine, University of Padua, via Giustiniani, 2-35128 Padua, Italy.
J Clin Med. 2020 May 6;9(5):1363. doi: 10.3390/jcm9051363.
Serotonin-secreting pancreatic neuroendocrine tumours (5-HT-secreting pNETs) are very rare, and characterised by high urinary 5-hydroxyindole-acetic acid (5-HIAA) levels (or high serum 5-HT levels).
Patients with 5-HT-secreting pancreatic neoplasms observed in our unit (1986-2015) were included. Diagnosis was based on urinary 5-HIAA or serum 5-HT levels.
Seven patients were enrolled (4 M/3 F), with a median age of 64 (range 38-69) years. Two patients had a carcinoid syndrome. Serum 5-HT was elevated in four patients. Urinary 5-HIAA levels were positive in six patients. The median tumour size was 4.0 (range 2.5-10) cm. All patients showed liver metastases at diagnosis. None underwent resective surgery; lymph node/liver biopsies were taken. Six lesions were well-differentiated tumours and one a poorly differentiated carcinoma (Ki67 range 3.4-70%). All but one patient received chemotherapy. Four patients received somatostatin analogues; three patients underwent ablation of liver metastases. One patient is alive with disease 117 months after observation. All the others died from disease progression after a follow-up within 158 months.
Primary 5-HT-secreting pNETs are mostly metastatic to the liver; patients are not amenable to resective surgery. Despite high 5-HIAA urinary levels, few patients present with carcinoid syndrome. A five-year survival rate of 42.9% may be achieved with multimodal treatment.
分泌5-羟色胺的胰腺神经内分泌肿瘤(5-HT分泌性pNETs)非常罕见,其特征为尿5-羟吲哚乙酸(5-HIAA)水平升高(或血清5-HT水平升高)。
纳入我院(1986 - 2015年)观察到的分泌5-HT的胰腺肿瘤患者。诊断基于尿5-HIAA或血清5-HT水平。
共纳入7例患者(4例男性/3例女性),中位年龄64岁(范围38 - 69岁)。2例患者出现类癌综合征。4例患者血清5-HT升高。6例患者尿5-HIAA水平呈阳性。肿瘤中位大小为4.0 cm(范围2.5 - 10 cm)。所有患者诊断时均有肝转移。无一例接受根治性手术;均进行了淋巴结/肝脏活检。6个病灶为高分化肿瘤,1个为低分化癌(Ki67范围3.4 - 70%)。除1例患者外,所有患者均接受了化疗。4例患者接受了生长抑素类似物治疗;3例患者进行了肝转移灶消融。1例患者在观察117个月后仍带瘤生存。其他所有患者在158个月内的随访中均因疾病进展死亡。
原发性5-HT分泌性pNETs大多转移至肝脏;患者不适合进行根治性手术。尽管尿5-HIAA水平较高,但很少有患者出现类癌综合征。多模式治疗可能实现42.9%的五年生存率。