Oliveira Lima Sonia, Rocha Santana Vanessa, Correia Leao Sydney, Faro Santos Paulo Sérgio, De Alburquerque Ricardo Luis Cavalcanti
Department of Medicine, University Hospital, Federal University of Sergipe, Aracaju, SE, Brazil.
Rev Med Chil. 2012 Sep;140(9):1179-84. doi: 10.4067/S0034-98872012000900012.
Solid-pseudopapillary tumor of pancreas is a rare neoplasm which occurs pre-dominantely in young females. This tumor generally is asymptomatic or minimally symptomatic and some imaging tests are useful for its diagnosis. We report a 17 years-old woman with dyspeptic symptoms submitted to an abdominal ultrasound (US), that revealed a hypoechogenic mass between the liver, right kidney and pancreas. Computer tomography (CT) scan showed a hypodense and heterogeneous mass on pancreas head. The patient underwent elective resection of the mass and the histopathology was consistent with a solid-pseudopapillary tumor of pancreas. Immunohistochemical positivity for NSE (neuron-specific enolase), progesterone receptor, alfa-1-antitrypsin, vimentin, AE1/AE3, and negativity for synaptophysin and chromogranin A confirmed the diagnosis. After four years of clinical follow-up, the patient remains in a good general condition without signs of tumor recurrence.
胰腺实性假乳头状瘤是一种罕见的肿瘤,主要发生于年轻女性。该肿瘤通常无症状或症状轻微,一些影像学检查对其诊断有用。我们报告一名17岁有消化不良症状的女性,接受腹部超声检查,发现肝脏、右肾和胰腺之间有一个低回声肿块。计算机断层扫描(CT)显示胰头有一个低密度且不均匀的肿块。患者接受了肿块的择期切除,组织病理学结果与胰腺实性假乳头状瘤一致。神经元特异性烯醇化酶(NSE)、孕激素受体、α1-抗胰蛋白酶、波形蛋白、AE1/AE3免疫组化呈阳性,突触素和嗜铬粒蛋白A呈阴性,确诊了该诊断。经过四年的临床随访,患者总体状况良好,无肿瘤复发迹象。