{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,18]],"date-time":"2026-05-18T04:39:46Z","timestamp":1779079186819,"version":"3.51.4"},"reference-count":8,"publisher":"SAGE Publications","issue":"2","license":[{"start":{"date-parts":[[2009,12,1]],"date-time":"2009-12-01T00:00:00Z","timestamp":1259625600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Rare Tumors"],"published-print":{"date-parts":[[2009,12,28]]},"abstract":"<jats:p>\n                    Lymphangiomas are congenital malformations of the lymphatic system that account for about 5% of all benign tumors in infants and children.\n                    <jats:sup>1<\/jats:sup>\n                    The most common sites are the neck and axilla, which account for 95% of cases.\n                    <jats:sup>2<\/jats:sup>\n                    Abdominal cystic lymphangiomas are quite rare, and can arise from either the retroperitoneum, gastrointestinal tract, or the mesentery of the abdominal viscera.\n                    <jats:sup>3<\/jats:sup>\n                    The presenting symptoms are painless abdominal distension, a palpable mass, or secondary complications in the abdomen such as intestinal obstruction, volvulus, intestinal infarction, or bleeding.\n                    <jats:sup>4<\/jats:sup>\n                    Typically diagnosed during childhood, these tumors prompt surgical intervention. We describe an atypical case of an abdominal cystic lymphangioma, which did not manifest until adulthood, with atypical symptoms of a rapidly expanding and symptomatic mass.\n                  <\/jats:p>","DOI":"10.4081\/rt.2009.e48","type":"journal-article","created":{"date-parts":[[2021,12,24]],"date-time":"2021-12-24T10:47:28Z","timestamp":1640342848000},"page":"148-149","source":"Crossref","is-referenced-by-count":9,"title":["Giant mesenteric cystic lymphangioma presenting with abdominal pain and masquerading as a gynecologic malignancy"],"prefix":"10.1177","volume":"1","author":[{"given":"John","family":"Maa","sequence":"first","affiliation":[{"name":"Department of Surgery, University of California, San Francisco, CA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christianne","family":"Wa","sequence":"additional","affiliation":[{"name":"University of Southern California, San Francisco, CA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Adnan","family":"Jaigirdir","sequence":"additional","affiliation":[{"name":"Department of Surgery, University of California, San Francisco, CA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Soo-Jin","family":"Cho","sequence":"additional","affiliation":[{"name":"Department of Anatomic Pathology, University of California, San Francisco, CA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carlos U","family":"Corvera","sequence":"additional","affiliation":[{"name":"Department of Surgery, University of California, San Francisco, CA, USA"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"179","published-online":{"date-parts":[[2009,12,1]]},"reference":[{"key":"bibr1-rt.2009.e48","first-page":"E42","volume":"5","author":"M\u00e9ndez-Gallart R","year":"2009","journal-title":"J Can Chir"},{"key":"bibr2-rt.2009.e48","doi-asserted-by":"publisher","DOI":"10.3348\/kjr.2009.10.3.319"},{"key":"bibr3-rt.2009.e48","first-page":"E265","volume":"48","author":"Prabhakaran K","year":"2007","journal-title":"Singapore Med J"},{"key":"bibr4-rt.2009.e48","doi-asserted-by":"publisher","DOI":"10.1007\/s10620-008-0674-3"},{"key":"bibr5-rt.2009.e48","doi-asserted-by":"crossref","first-page":"395","DOI":"10.1046\/j.1365-2168.1998.00628.x","volume":"85","author":"de Perrot M","year":"1998","journal-title":"Br J Surg"},{"key":"bibr6-rt.2009.e48","doi-asserted-by":"publisher","DOI":"10.1016\/j.jpedsurg.2008.01.075"},{"key":"bibr7-rt.2009.e48","doi-asserted-by":"publisher","DOI":"10.1089\/lap.2007.0145"},{"key":"bibr8-rt.2009.e48","doi-asserted-by":"publisher","DOI":"10.1159\/000102896"}],"container-title":["Rare Tumors"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/journals.sagepub.com\/doi\/pdf\/10.4081\/rt.2009.e48","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/journals.sagepub.com\/doi\/full-xml\/10.4081\/rt.2009.e48","content-type":"application\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/journals.sagepub.com\/doi\/pdf\/10.4081\/rt.2009.e48","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T05:33:27Z","timestamp":1777613607000},"score":1,"resource":{"primary":{"URL":"http:\/\/journals.sagepub.com\/doi\/10.4081\/rt.2009.e48"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,12,1]]},"references-count":8,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2009,12,28]]}},"alternative-id":["10.4081\/rt.2009.e48"],"URL":"https:\/\/doi.org\/10.4081\/rt.2009.e48","relation":{},"ISSN":["2036-3613","2036-3613"],"issn-type":[{"value":"2036-3613","type":"print"},{"value":"2036-3613","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,12,1]]}}}