{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T23:36:09Z","timestamp":1768433769740,"version":"3.49.0"},"reference-count":8,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","license":[{"start":{"date-parts":[[2013,1,1]],"date-time":"2013-01-01T00:00:00Z","timestamp":1356998400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2013,7,16]],"date-time":"2013-07-16T00:00:00Z","timestamp":1373932800000},"content-version":"vor","delay-in-days":196,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/3.0\/"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2013,1]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>INTRODUCTION:<\/jats:title>\n                    <jats:p>Pancreatic tumor is a rare condition in children, but reasonably common in adults. Histopathology in children also differs from that in adults, with most cases being pancreatoblastoma, solid pseudopapillary tumor, or pancreatic endocrine tumors.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>PRESENTATION OF CASE:<\/jats:title>\n                    <jats:p>A 14-month-old boy was noticed abdominal distension and referred to our hospital. Laboratory findings revealed leukocytosis and elevation of serum level of C-reactive protein and pancreatic enzymes. Radiological findings at admission were the huge abdominal cyst in abdominal computed tomography. As the levels of pancreatic enzyme elevated synchronous to oral feeding, total parenteral nutrition was needed. Besides radiographically the abdominal lesion changed from multiple large cystic type to multiple microcystic lesion including solid component over time. It was considered different diagnosis was pancreatic blastoma, pancreatic pseudo cyst, and lymphangioma and he was performed operation. The huge multicystic and partially solid tumor arising from the tail of pancreas existed from posterior of stomach to pelvic cavity. The tumor was completely resected without pancreatectomy and residual pancreas can be kept without tumor invasion. Histopathological finding was pancreatic hamartoma.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>DISCUSSION:<\/jats:title>\n                    <jats:p>Pancreatic hamartoma was extremely rare, and only 17 cases were previously reported in the literature. This is the first case that the change of radiographic findings overtime was shown. We reviewed 17 cases (4 cases in children) of pancreatic hamartoma including our case.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>CONCLUSION:<\/jats:title>\n                    <jats:p>Although extremely rare, pancreatic hamartoma should be considered in the differential diagnosis of cystic abdominal mass in children.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1016\/j.ijscr.2012.10.001","type":"journal-article","created":{"date-parts":[[2012,10,8]],"date-time":"2012-10-08T17:39:38Z","timestamp":1349717978000},"page":"98-100","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":24,"title":["Multicystic adenomatoid pancreatic hamartoma in a child"],"prefix":"10.1097","volume":"4","author":[{"given":"Ryo","family":"Sueyoshi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tadaharu","family":"Okazaki","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Geoffrey J.","family":"Lane","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Atsushi","family":"Arakawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takashi","family":"Yao","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Atsuyuki","family":"Yamataka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-28-20260114","doi-asserted-by":"crossref","first-page":"314","DOI":"10.2350\/07-04-0260.1","article-title":"Multicystic adenomatoid hamartoma of the pancreas: a hitherto undescribed pancreatic tumor occurring in a 3-year-old boy","volume":"11","author":"Thrall","year":"2008","journal-title":"Pediatric and Developmental Pathology"},{"key":"R2-28-20260114","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1097\/00000478-198306000-00003","article-title":"Tumors of the exocrine pancreas in children and adolescents. A clinical and pathologic study of eight cases","volume":"7","author":"Lack","year":"1983","journal-title":"American Journal of Surgical Pathology"},{"key":"R3-28-20260114","first-page":"154","article-title":"Uber hamartoma","volume":"7","author":"Albrecht","year":"1904","journal-title":"Verhandlungen der Deutschen Gesellschaft fur Pathologie"},{"key":"R4-28-20260114","doi-asserted-by":"crossref","first-page":"276","DOI":"10.1111\/j.1440-1827.2007.02090.x","article-title":"Solid pancreatic hamartoma","volume":"57","author":"Nagata","year":"2007","journal-title":"Pathology International"},{"key":"R5-28-20260114","doi-asserted-by":"crossref","first-page":"797","DOI":"10.1097\/01.pas.0000157748.18591.d7","article-title":"Pancreatic solid and cystic hamartoma in adults: characterization of a new tumorous lesion","volume":"29","author":"Pauser","year":"2005","journal-title":"American Journal of Surgical Pathology"},{"key":"R6-28-20260114","doi-asserted-by":"crossref","first-page":"1211","DOI":"10.1038\/modpathol.3800406","article-title":"Cellular hamartoma resembling gastrointestinal stromal tumor: a solid tumor of the pancreas expressing c-kit (CD117)","volume":"18","author":"Pauser","year":"2005","journal-title":"Modern Pathology"},{"key":"R7-28-20260114","doi-asserted-by":"crossref","first-page":"1309","DOI":"10.1016\/0046-8177(92)90301-I","article-title":"Multicystic pancreatic hamartoma: a distinctive lesion with immunohistochemical and ultrastructural study","volume":"23","author":"Flaherty","year":"1992","journal-title":"Human Pathology"},{"key":"R8-28-20260114","first-page":"483","article-title":"Pancreatic hamartoma and SAPHO syndrome: a case report","volume":"18","author":"Sampelean","year":"2009","journal-title":"Journal of Gastrointestinal and Liver Diseases: JGLD"}],"container-title":["International Journal of Surgery Case Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261212001769?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S2210261212001769?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/journals.lww.com\/01612930-201304010-00028","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,1,14]],"date-time":"2026-01-14T13:20:56Z","timestamp":1768396856000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/01612930-201304010-00028"}},"subtitle":["Case report and literature review"],"short-title":[],"issued":{"date-parts":[[2013,1]]},"references-count":8,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2013]]}},"URL":"https:\/\/doi.org\/10.1016\/j.ijscr.2012.10.001","relation":{},"ISSN":["2210-2612"],"issn-type":[{"value":"2210-2612","type":"print"}],"subject":[],"published":{"date-parts":[[2013,1]]}}}