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Giant Mucinous Cystadenoma Of The Pancreas: A Rare Aetiology Of An Abdominal Tumor, A Case Report

机译:胰腺巨大粘液性囊腺瘤:腹部肿瘤的罕见病因,一例报告

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Cystic tumors of the pancreas represent less than 10 % of all the cystic hurts of this organ. Among them, mucinous cystadenomas constitute a very particular anatomo-pathological entity with malignant potential. The purpose of this work is to report a particular case by its clinical presentation display, its size, and the surgical treatment which ensued. We discuss the diagnostic and therapeutic aspects of this condition. Introduction Cystic tumors of the pancreas represent less than 10 % of all the cystic conditions of this organ. Among them, mucinous cystadenomas constitute a very particular anatomo-pathological entity. This pathology defines itself as being a cystic tumor with malignant potential. Its preoperative diagnosis is increasingly refined by the advances of the imaging combined in the draining cystic intra under echo-endoscopy. The purpose of this case report is to describe a particular case by its clinical presentation, its size, and its surgical treatment. We discuss the diagnostic and therapeutic aspects of this condition. Observation A 30-year-old patient, without particular pathological histories was admitted for an abdominal tumefaction evolving during the past 8 months associated with epigastric abdominal pain and occasional vomiting which calmed the pain. On examination, we found a patient in good general condition with normal constants, an enormous abdominal mass measuring 15cm on 20cm, firm, painless, mobile compared with the superficial plan. Laboratory investigations showed an anaemia with a rate of haemoglobin in 9,9g / dl.The tomodensitometry showed (figure 1) a voluminous cystic mass with fine walls contrast enhancing and developed at the pancreas tail. There were no partitions either of vegetations or calcifications. The neighboring pancreatic parenchyma was of normal aspect and Wirsung duct was not dilated.The dosage of plasmatic C19-9 had returned normal for 15,7 KU / L.During median laparotomy we found a voluminous cystic mass of the pancreas tail (figure 2) which contracted multiple adhesions with the transverse colon, small bowel, left kidney and its vein, and the splenic pedicle.After careful dissection, a left splenopancreatectomy taking the tumor was realized associated with an resection-anastomosis of the adjacent transverse colon. The post-operative care consisted of a triple vaccination (anti meningococcus, anti pneumococcus and anti Haemophilus influenzae) and an antibioprophylaxy with Oracilline. Surgical pathology showed a cystic formation which weighed 4kg with thick and fibrous wall lined on its internal face by a cylindrical epithelial cover secreting mucus. We found some islands of endocrine atrophic cells in periphery or in the shell. There were no suspicious signs of wickedness. The pancreatic section was healthy. The examination ended in a diagnosis of pancreatic mucinous cystadenoma without formal histological signs of wickedness. Discussion Cystic tumors of the pancreas represent 10 to 15 % of all the pancreatic cysts and approximately 1 % of the pancreatic cancers [1]. The mucinous cystadenoma is a tumor slow in devolvement and does not tend to regression. It is a macrocystic tumor united or oligo cystic (less than 6 cysts) limited by a cylindrical mucinous secreting epithelium basing on a pseudo-ovarian stroma with richl cellular content.The ascendancy is feminine with an average age of 60 years as described by Hardacre [1,2]. However, this pathology was also found in patients much younger as in our case [1,4].The clinical signs are not specific. The discovery is increasingly fortuitous with the progress of imaging. Our patient was symptomatic and presented with epigastric pains and abdominal mass.The morphological diagnosis calls on to the combination of several examinations in particular the ultrasound, the Scanner, the MRI, the echo-endoscopy. All these examinations complement each other and their association allows to increase the efficiency of the diagnosis. Lewin [5] co
机译:胰腺的囊性肿瘤占该器官所有囊性损伤的不到10%。其中,粘液性囊腺瘤构成非常特殊的具有恶性潜能的解剖病理学实体。这项工作的目的是通过临床表现展示,大小和随后的手术治疗来报告特定病例。我们讨论了这种情况的诊断和治疗方面。简介胰腺囊性肿瘤占该器官所有囊性疾病的不到10%。其中,粘液性囊腺瘤构成非常特殊的解剖病理学实体。这种病理学将自身定义为具有恶性潜能的囊性肿瘤。通过超声内镜在引流性胆囊内成像的结合,其术前诊断日益完善。本病例报告的目的是通过临床表现,大小和手术治疗来描述特定病例。我们讨论了这种情况的诊断和治疗方面。观察一名30岁,无特殊病史的患者因过去8个月内发生上腹部肿胀,伴上腹部腹痛并偶尔呕吐使疼痛平息而入院。在检查中,我们发现患者的身体状况良好,常数恒定,与腹部计划相比,腹部巨大的腹部肿块在20cm处长15cm,结实,无痛,活动自如。实验室检查显示贫血的血红蛋白比率为9.9 g / dl。通透光度法显示(图1)巨大的囊性肿块,其细小壁对比度增强并在胰腺尾部发育。没有植被或钙化的分区。邻近的胰腺实质状态正常,Wirsung导管未扩张。血浆C19-9剂量已恢复正常1,57 KU / L.在剖腹正中切开术中,我们发现胰腺尾部有一个巨大的囊性肿块(图2)并与横结肠,小肠,左肾及其静脉,脾蒂发生多处粘连。仔细解剖后,发现左脾胰脏切除术伴有肿瘤,并与邻近横结肠切除吻合。术后护理包括三重疫苗接种(抗脑膜炎球菌,抗肺炎球菌和抗流感嗜血杆菌)和使用Oracilline进行生物预防。手术病理显示为一个囊性结构,重4kg,内壁上有一层厚厚的纤维壁,壁上有一层分泌粘液的圆柱形上皮覆盖物。我们在外围或外壳中发现了一些内分泌萎缩细胞岛。没有可疑的邪恶迹象。胰腺部分健康。这项检查最终诊断出胰腺粘液性囊腺瘤,没有正式的组织学上的邪恶迹象。讨论胰腺囊性肿瘤占所有胰腺囊肿的10%至15%,约占胰腺癌的1%[1]。粘液性囊腺瘤是肿瘤进展缓慢且不倾向于消退的肿瘤。它是一种大囊性肿瘤,由一个圆柱形的粘液状分泌上皮细胞或一个多囊性的少见的囊性肿瘤(少于6个囊肿)所组成,其上皮细胞的细胞含量较高,是假卵巢基质。其优势是女性,平均年龄为60岁,如Hardacre [ 1,2]。然而,这种病理也被发现在与我们的病例相比年轻的患者中[1,4]。临床体征不是特异性的。这一发现随着成像技术的发展越来越偶然。我们的患者有症状,表现为上腹部疼痛和腹部肿块。形态学诊断要求结合多种检查,尤其是超声,扫描仪,MRI,回声内窥镜检查。所有这些检查是相辅相成的,它们的关联可以提高诊断的效率。列文[5]

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