Thavaraputta Subhanudh, Graham Suzanne, Rivas Mejia Ana M, Lado-Abeal Joaquin
Department of Internal Medicine, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.
Department of Pathology, Texas Tech Univeristy Health Sciences Center, Lubbock, Texas, USA.
BMJ Case Rep. 2019 Jan 10;12(1):bcr-2018-226702. doi: 10.1136/bcr-2018-226702.
Somatostatinomas are rare neuroendocrine tumours, mostly located in the pancreas or duodenum, with an estimated incidence of 1 in 40 million. Duodenal somatostatinomas (DSs) are usually found in association with neurofibromatosis type 1 (NF1), tuberous sclerosis and Von Hippel-Lindau syndrome. Gastrointestinal stromal tumours (GIST) have also been described in NF1, but the association with somatostatinoma is very uncommon. We report the case of a patient with NF1 who presented with obstructive jaundice due to multiple firm nodules around the ampulla of Vater. A pancreaticoduodenectomy was performed and revealed a 1 cm duodenal/ampullary mass which stained positive for somatostatin, together with a GIST also found on the duodenal wall. Despite its rarity, ampullary somatostatinomas should be considered in the differential diagnosis of biliary tract dilation in patients with NF1.
生长抑素瘤是一种罕见的神经内分泌肿瘤,大多位于胰腺或十二指肠,估计发病率为四千分之一。十二指肠生长抑素瘤(DSs)通常与1型神经纤维瘤病(NF1)、结节性硬化症和冯·希佩尔-林道综合征相关。胃肠道间质瘤(GIST)也在NF1中有所描述,但与生长抑素瘤的关联非常罕见。我们报告了一例NF1患者,该患者因 Vater壶腹周围多个实性结节出现梗阻性黄疸。行胰十二指肠切除术,发现一个1厘米的十二指肠/壶腹肿块,生长抑素染色呈阳性,同时在十二指肠壁上也发现了一个GIST。尽管罕见,但在NF1患者胆道扩张的鉴别诊断中应考虑壶腹生长抑素瘤。