Lymphangioma of the pancreas with "ovarian-like" mesenchymal stroma: a case report with emphasis on histogenesis
Pancreatic lymphangiomas, which occur predominantly in women, are rare and account for only 1% of all lymphangiomas. The characteristic histologic features include multiple cysts lined by endothelial cells, irregularly distributed smooth muscle cells, and lymphoid aggregates in the wall of the cyst....
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2003-11, Vol.127 (11), p.1513-1516 |
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container_title | Archives of pathology & laboratory medicine (1976) |
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creator | Gui, Lizhen Bigler, Steven A Subramony, Charu |
description | Pancreatic lymphangiomas, which occur predominantly in women, are rare and account for only 1% of all lymphangiomas. The characteristic histologic features include multiple cysts lined by endothelial cells, irregularly distributed smooth muscle cells, and lymphoid aggregates in the wall of the cyst. We describe a 36-year-old woman with lymphangioma of the pancreas with "ovarian-like" mesenchymal stroma in the wall. This stroma, composed of uncommitted mesenchymal cells, has not been described previously in the wall of pancreatic lymphangiomas. Multiple small lymphatic channels that are found in this stroma recapitulate the development of lymphatic channels in the embryo. Lymphangioma of the pancreas may arise from distension of these lymphatic channels. Pancreatic lymphangioma may, therefore, be a developmental anomaly rather than a true neoplasm. |
doi_str_mv | 10.5858/2003-127-1513-LOTPWO |
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The characteristic histologic features include multiple cysts lined by endothelial cells, irregularly distributed smooth muscle cells, and lymphoid aggregates in the wall of the cyst. We describe a 36-year-old woman with lymphangioma of the pancreas with "ovarian-like" mesenchymal stroma in the wall. This stroma, composed of uncommitted mesenchymal cells, has not been described previously in the wall of pancreatic lymphangiomas. Multiple small lymphatic channels that are found in this stroma recapitulate the development of lymphatic channels in the embryo. Lymphangioma of the pancreas may arise from distension of these lymphatic channels. Pancreatic lymphangioma may, therefore, be a developmental anomaly rather than a true neoplasm.</description><identifier>ISSN: 0003-9985</identifier><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.5858/2003-127-1513-LOTPWO</identifier><identifier>PMID: 14567749</identifier><identifier>CODEN: APLMAS</identifier><language>eng</language><publisher>United States: College of American Pathologists</publisher><subject>Adult ; Female ; Humans ; Lymphangioma - diagnosis ; Mesoderm - pathology ; Multipotent Stem Cells - pathology ; Ovary - pathology ; Pancreatic Neoplasms - diagnosis ; Stromal Cells - pathology</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2003-11, Vol.127 (11), p.1513-1516</ispartof><rights>Copyright College of American Pathologists Nov 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c262t-d1f543042cd6466629ef20e6936bb81ee0a3fb9789cb8398ce5d0183c5556eb53</citedby><cites>FETCH-LOGICAL-c262t-d1f543042cd6466629ef20e6936bb81ee0a3fb9789cb8398ce5d0183c5556eb53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14567749$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gui, Lizhen</creatorcontrib><creatorcontrib>Bigler, Steven A</creatorcontrib><creatorcontrib>Subramony, Charu</creatorcontrib><title>Lymphangioma of the pancreas with "ovarian-like" mesenchymal stroma: a case report with emphasis on histogenesis</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Pancreatic lymphangiomas, which occur predominantly in women, are rare and account for only 1% of all lymphangiomas. 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Pancreatic lymphangioma may, therefore, be a developmental anomaly rather than a true neoplasm.</description><subject>Adult</subject><subject>Female</subject><subject>Humans</subject><subject>Lymphangioma - diagnosis</subject><subject>Mesoderm - pathology</subject><subject>Multipotent Stem Cells - pathology</subject><subject>Ovary - pathology</subject><subject>Pancreatic Neoplasms - diagnosis</subject><subject>Stromal Cells - pathology</subject><issn>0003-9985</issn><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkUtLxDAUhYMoOj7-gUiYhbtqHk2auBPxBQO6UFyGNHNrq21Tk44y_96UGRBcXQ6cc7j3fgidUnIhlFCXjBCeUVZkVFCeLZ5ent-edtCMipxnjEqxi2ZksmitxAE6jPEjSc0Y3UcHNBeyKHI9Q8Ni3Q217d8b31nsKzzWgAfbuwA24p9mrPHcf9vQ2D5rm0-Y4w4i9K5ed7bFcQwpdoUtdjYCDjD4MG5SMNXGJmLf47qJo3-HHpI-RnuVbSOcbOcRer27fbl5SBfcP95cLzLHJBuzJa3SISRnbilzKSXTUDECUnNZlooCEMurUhdKu1JxrRyIJaGKOyGEhFLwI3S-6R2C_1pBHE3XRAdta3vwq2gKyhQRBUnG-T_jh1-FPu1mGGVEFlRMbfnG5IKPMUBlhtB0NqwNJWbCYSYcJuEwEw6zwZFiZ9vuVdnB8i-0_T__BTDChxY</recordid><startdate>200311</startdate><enddate>200311</enddate><creator>Gui, Lizhen</creator><creator>Bigler, Steven A</creator><creator>Subramony, Charu</creator><general>College of American Pathologists</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQGLB</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>200311</creationdate><title>Lymphangioma of the pancreas with "ovarian-like" mesenchymal stroma: a case report with emphasis on histogenesis</title><author>Gui, Lizhen ; 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source | MEDLINE; Allen Press Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
subjects | Adult Female Humans Lymphangioma - diagnosis Mesoderm - pathology Multipotent Stem Cells - pathology Ovary - pathology Pancreatic Neoplasms - diagnosis Stromal Cells - pathology |
title | Lymphangioma of the pancreas with "ovarian-like" mesenchymal stroma: a case report with emphasis on histogenesis |
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