Miloudi Nizar, Hefaiedh Rania, Marzouk Inès, Gharbi Lassad, Khalfallah Med Tahar
Tunis Med. 2015 Mar;93(3):184-6.
Solid pseudopapillary tumors of the pancreas are rare. The diagnosis is difficult because of its clinical and radiological polymorphism. It was described in the literature that this entity can be associated with congenital malformation. We report an exceptional case associating solid pseudopapillary tumor of the pancreas to Bochdalek's hernia.
A 31 year-old woman presented with abdominal pain. Radiological findings (ultrasound, CT scan, MRI) showed a heterogeneous mass evoking a stromal tumor of duodenal origin associated to a hernia through the foramen of Bochdalek. The patient underwent tumorectomy without lymphadenectomy with a hernia repair. Pathology report confirmed the diagnosis of solid pseudopapillary tumor of the pancreas. The 3-years follow- up was uneventful.
Solid pseudopapillary tumor of the pancreas is a rare benign tumor with a good prognosis after resection. Recognition of the association of congenital malformation with solid pseudopapillary tumor of the pancreas is useful as it could have implications on the diagnosis and treatment.
胰腺实性假乳头状瘤较为罕见。由于其临床和影像学表现具有多态性,诊断较为困难。文献报道该实体可与先天性畸形相关。我们报告一例胰腺实性假乳头状瘤合并博赫dalek疝的特殊病例。
一名31岁女性因腹痛就诊。影像学检查结果(超声、CT扫描、MRI)显示一个异质性肿块,提示十二指肠起源的间质瘤,并伴有通过博赫dalek孔的疝。患者接受了肿瘤切除术,未进行淋巴结清扫,并进行了疝修补术。病理报告证实为胰腺实性假乳头状瘤。3年随访无异常。
胰腺实性假乳头状瘤是一种罕见的良性肿瘤,切除后预后良好。认识到先天性畸形与胰腺实性假乳头状瘤的关联有助于诊断和治疗。