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Clinicopathological and immunohistochemical study of 29 cases of solid-pseudopapillary neoplasms of the pancreas in patients under 20?years of age along with detailed review of literature

机译:临床病理学和免疫组化研究20岁以下患者胰腺胰腺固体尾状肿瘤29例及文献详细综述

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Abstract Background Pancreatic Solid Pseudopapillary Neoplasms (SPNs) are rare low-grade malignant tumors with a marked preponderance for young females. Objective was to describe the morphology, differential diagnosis, and prognosis of SPNs in patients under 20?years of age and present a detailed review of literature. Methods A total of 29 cases in patients under 20?years of age reported as SPN during the period January 2014 to December 2019, were included in the study. These included 19 resection specimens, 4 incision biopsies and 6 cases received as blocks for second opinion. Hematoxylin and eosin (H&E) slides as well as immunohistochemistry (IHC) slides of all cases were retrieved and reviewed by the authors. TFE3 and Progesterone Receptor were performed retrospectively. Results Twenty-eight of the 29 patients were females. Ages of patients ranged from 12 to 19?years. Nineteen cases were resections. Tail was the commonest location. Mean tumor size was 9.5?cm. In 89.5% cases, tumor was confined to the pancreas. In 2 cases, distant metastasis was present. In 2 cases, extension beyond pancreas was seen. Solid and pseudopapillary areas were seen in all cases while other features were variable. Beta catenin and Cyclin D1 were positive in most cases while TFE3 was positive in 57% cases. Progesterone Receptor (PR) was positive in all 13 cases in which it was performed. Follow up was available in 14 patients. Follow up period ranged from 3 to 70?months. Twelve were alive and well without recurrence or metastasis while 2 were alive with recurrence and metastasis to liver and omentum respectively. Conclusions Although many studies on SPNs have been published, surgeons, oncologists and even pathologists in this part of the world are often not aware of these rare tumors leading to inaccuracies and delays in diagnosis. In addition, this paper focusses on the interesting observation that the majority of SPNs diagnosed in our department during study period occurred in patients under 20?years of age (29 versus 21 in patients over 20). However, clinico-epidemiological, morphologic and prognostic features were similar in both age groups. Possibility of SPNs should always be considered in case of pancreatic neoplasms occurring in patients under 20?years of age as well. We believe that this is a very interesting and helpful study for the clinicians as well as the pathologists.
机译:摘要背景胰腺固体假缺陷肿瘤(SPN)是罕见的低级恶性肿瘤,对于年轻女性而言,具有标记优势。目的是描述20岁以下患者的SPN的形态,鉴别诊断和预后,并对文献进行了详细审查。方法在2014年1月至2019年12月期间,20岁以下的患者共29例,截至2019年1月至2019年12月。这些包括19分切除试样,4个切口活检,6例作为第二意见的块收到。血杂志和曙红(H&E)载玻片以及免疫组化(IHC)所有病例的载玻片都被作者审查并审查。回顾性地进行TFE3和孕酮受体。结果29例患者中有28名是女性。年龄的患者从12到19岁到19年。多年。十九病例分解。尾巴是最常见的地方。平均肿瘤大小为9.5?cm。在89.5%的病例中,肿瘤被局限于胰腺。在2例中,存在远处转移。在2例中,看到胰腺超出胰腺。在所有情况下都可以看到固体和假缺陷区域,而其他特征是可变的。在大多数情况下,βCatenin和Cyclin D1是阳性的,而TFE3在57%的情况下为阳性。在其进行的所有13例中,孕酮受体(PR)是阳性的。随访14名患者。跟进时间为3到70?几个月。十二个活着,良好,没有复发或转移,而2分别对肝脏和全膜恢复和转移。结论虽然对SPN的许多研究已经出版,外科医生,肿瘤医学家甚至在世界上的病理学家往往不了解这些罕见的肿瘤,导致诊断不准确和延迟。此外,本文侧重于有趣的观察,即在20岁以下的患者患者中诊断的大多数SPNS发生在20岁以下的患者(29例,超过20岁的患者。然而,两岁群体中临床流行病学,形态学和预后特征相似。如果在20岁以下的患者中发生胰腺肿瘤的情况下,应始终考虑SPN的可能性。我们相信这对临床医生以及病理学家来说是一个非常有趣和有助于的研究。

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