Omental acinar cell carcinoma of pancreatic origin in a child: a clinicopathological rarity

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• 作者：Shilpa Sharma ; Shipra Agarwal ; Murali Krishna Nagendla…
• 关键词：Heterotopic pancreatic tumor ; Omentum ; Acinar cell carcinoma
• 刊名：Pediatric Surgery International
• 出版年：2016
• 出版时间：March 2016
• 年：2016
• 卷：32
• 期：3
• 页码：307-311
• 全文大小：1,218 KB
• 参考文献：1.Dolan RV, ReMine WH, Dockerty MB (1974) The fate of heterotopic pancreatic tissue. A study of 212 cases. Arch Surg 109:762–765CrossRef PubMed
  2.Papaziogas B, Koutelidakis I, Tsiaousis P, Panagiotopoulou K, Paraskevas G, Argiriadou H, Atmatzidis S, Atmatzidis K (2008) Carcinoma developing in ectopic pancreatic tissue in the stomach: a case report. Cases J 1:249PubMedCentral CrossRef PubMed
  3.Yang X, Wang X (2010) Imaging findings of pancreatoblastoma in 4 children including a case of ectopic pancreatoblastoma. Pediatr Radiol 40:1609–1614CrossRef PubMed
  4.Yang ZH, Gao JB, Yue SW, Yang XH, Guo H (2011) Synchronous ectopic pancreatoblastoma in a child: a case report. J Korean Med Sci 26:832–835PubMedCentral CrossRef PubMed
  5.Ogata H, Oshio T, Ishibashi H, Takano S, Yagi M (2008) Heterotopic pancreas in children: review of the literature and report of 12 cases. Pediatr Surg Int 24:271–275CrossRef PubMed
  6.Guillou L, Nordback P, Gerber C, Schneider RP (1994) Ductal adenocarcinoma arising in a heterotopic pancreas situated in a hiatal hernia. Arch Pathol Lab Med 118:568–571PubMed
  7.Tez M, Ozalp N, Zulfikaroglu B, Koc M (2010) A solid pseudopapillary tumour arising from mesocolon without ectopic pancreas. HPB Surg. doi:10.​1155/​2010/​206186 PubMedCentral PubMed
  8.Ishikawa O, Ishiguro S, Ohhigastii H, Sasaki Y, Yasuda T, Imaoka S, Iwanaga T, Nakaizumi A, Fujita M, Wada A (1990) Solid and papillary neoplasm arising from an ectopic pancreas in the mesocolon. Am J Gastroenterol 85:597–601PubMed
  9.Sirasanagandla SR, Nayak SB, Bhat Kumar MR, Manipal M (2013) A rare congenital anomaly of the pancreas: a cadaveric case report. JOP. J Pancreas 14:454–457
  10.La Rosa S, Sessa F, Capella C (2015) Acinar cell carcinoma of the pancreas: overview of clinicopathologic features and insights into the molecular pathology. Front Med 2:41
  11.Klimstra DS, Heffess CS, Oertel JE, Rosai J (1992) Acinar cell carcinoma of the pancreas. A clinicopathologic study of 28 cases. Am J Surg Pathol 16:815–837CrossRef PubMed
  12.Maragliano R, Vanoli A, Albarello L, Milione M, Basturk O, Klimstra DS et al (2015) ACTH-secreting pancreatic neoplasms associated with Cushing syndrome: clinicopathologic study of 11 cases and review of the literature. Am J Surg Pathol 39:374–382CrossRef PubMed
  13.Rosai J (2011) Pancreas and Ampullary region. In: Rosai J (ed) Rosai and Ackerman’s Surgical Pathology, vol 1, 10th edn. Elsevier, London, pp 1024-1026
  14.Abraham SC, Wu T-T, Hruban RH, Lee JH, Yeo CJ, Conlon K et al (2002) Genetic and immunohistochemical analysis of pancreatic acinar cell carcinoma: frequent allelic loss on chromosome 11p and alteration in the APC/beta-catenin pathway. Am J Pathol 160:953–962PubMedCentral CrossRef PubMed
  15.Ordóñez NG, Mackay B (2000) Acinar cell carcinoma of the pancreas. Ultrastruct Pathol 24:227–241CrossRef PubMed
  16.Chaudhary P (2015) Acinar cell carcinoma of the pancreas: a literature review and update. Indian J Surg 77:226–231CrossRef PubMed
  
• 作者单位：Shilpa Sharma (1)
  Shipra Agarwal (2)
  Murali Krishna Nagendla (1)
  Devendra K. Gupta (1)
  
  1. Department of Pediatric Surgery, All India Institute of Medical Sciences, Ansari Nagar, New Delhi, 110029, India
  2. Department of Pathology, All India Institute of Medical Sciences, New Delhi, India
  
• 刊物类别：Medicine
• 刊物主题：Medicine & Public Health
  Pediatrics
  Surgery
  Pediatric Surgery
  
• 出版者：Springer Berlin / Heidelberg
• ISSN：1437-9813

文摘

A 6-year-old boy presented with a large subhepatic mass associated with pain abdomen. Exploration revealed a tumor in lesser omentum, completely separate from the normal pancreas that was excised completely. Histopathology suggested acinar cell carcinoma of pancreatic origin in an ectopic location. The child is well at 5 months follow-up.