Zavras Nikolaos, Schizas Demetrios, Machairas Nikolaos, Damaskou Vasileia, Economopoulos Nikolaos, Machairas Anastasios
Third Department of Surgery, University Hospital 'ATTIKON', 12462 Athens, Greece.
Second Department of Surgery, University Hospital 'Laiko', 11527 Athens, Greece.
Oncol Lett. 2017 Apr;13(4):2373-2376. doi: 10.3892/ol.2017.5678. Epub 2017 Feb 6.
A carcinoid tumor of the pancreas (CTP) is a rare pancreatic neoplasm, and usually presents with carcinoid syndrome (CS). CS consists of the classic symptom triad of cutaneous flushing, diarrhea and valvular disease, and occurs in the majority of patients with liver metastases. In the present study, the patient presented with symptoms of CS. A diagnosis of CTP with CS was suspected due to high levels of urine 5-hydroxyindolacetic acid, and this was confirmed by a fine-needle aspiration biopsy. Computed tomography showed extended lymphadenopathy, but no liver metastases. The patient was managed conservatively with octreotide long acting repeatable. To the best of our knowledge, this is the second literature case of CS associated with CTP without liver metastases.
胰腺类癌肿瘤(CTP)是一种罕见的胰腺肿瘤,通常表现为类癌综合征(CS)。CS由皮肤潮红、腹泻和瓣膜病这一典型症状三联征组成,多数有肝转移的患者会出现该症状。在本研究中,该患者出现了CS症状。由于尿5-羟吲哚乙酸水平升高,怀疑患有伴有CS的CTP,细针穿刺活检证实了这一诊断。计算机断层扫描显示有广泛的淋巴结病,但无肝转移。该患者采用长效可重复使用的奥曲肽进行保守治疗。据我们所知,这是第二例文献报道的伴有CTP且无肝转移的CS病例。