Congenital Cystic Tumors of the Atrio-Ventricular Node
Identifieur interne : 002535 ( Istex/Corpus ); précédent : 002534; suivant : 002536Congenital Cystic Tumors of the Atrio-Ventricular Node
Auteurs : Sally E. FordSource :
- Cardiovascular Pathology [ 1054-8807 ] ; 1999.
Abstract
Pathologists are dissuaded from the pathological study of the conduction system by the high cost and complexity of a traditional complete study. However, a simplified, low-cost approach can produce concrete information when performed in carefully selected cases of atrioventricular block, as demonstrated in the two cases of congenital cystic tumor of the atrioventricular node described in this report.
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DOI: 10.1016/S1054-8807(99)00013-7
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Ford</name><affiliation><mods:affiliation>Department of Pathology, Queen's University & Kingston General Hospital, Kingston, Ontario, Canada</mods:affiliation></affiliation><affiliation><mods:affiliation>Address for correspondence: Dr. Sally E. Ford, Department of Pathology, Richardson Laboratory, RM 201, Queen's University, Kingston, Ontario. 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B shows the excised block of tissue, which was then sliced vertically. The far right portion of the block was discarded as being too far into the membranous septum. C shows the block cut into pieces, with one side inked to prevent examination of contiguous sections</note><note type="content">Figure 2: The normal position of the node in Case 1 is occupied by clefts and nests of tumor in a connective tissue matrix. The tumor extends into one of the strands of a coronary sinus web (W)</note><note type="content">Figure 3: The clefts are lined with cuboidal epithelioid cells (A), which stained positive for cytokeratin in Case 2 (B). This stain was positive in both cases, as was carcino-embryonic antigen</note><note type="content">Table 1: Histochemical and Immunohistochemical Characteristics of the Tumors</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a">Congenital Cystic Tumors of the Atrio-Ventricular Node</title><title level="a" type="sub">Successful Demonstration by an Abbreviated Dissection of the Conduction System</title><author xml:id="author-0000"><persName><forename type="first">Sally E</forename><surname>Ford</surname></persName><roleName type="degree">MBBS, FRCPC</roleName><email>ford@cliff.path.queensu.ca</email><affiliation>Department of Pathology, Queen's University & Kingston General Hospital, Kingston, Ontario, Canada</affiliation><affiliation>Address for correspondence: Dr. Sally E. Ford, Department of Pathology, Richardson Laboratory, RM 201, Queen's University, Kingston, Ontario. 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However, a simplified, low-cost approach can produce concrete information when performed in carefully selected cases of atrioventricular block, as demonstrated in the two cases of congenital cystic tumor of the atrioventricular node described in this report.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>Congenital Cystic Tumors of the Atrio-Ventricular Node</title><subTitle>Successful Demonstration by an Abbreviated Dissection of the Conduction System</subTitle></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>Congenital Cystic Tumors of the Atrio-Ventricular Node</title><subTitle>Successful Demonstration by an Abbreviated Dissection of the Conduction System</subTitle></titleInfo><name type="personal"><namePart type="given">Sally E</namePart><namePart type="family">Ford</namePart><namePart type="termsOfAddress">MBBS, FRCPC</namePart><affiliation>Department of Pathology, Queen's University & Kingston General Hospital, Kingston, Ontario, Canada</affiliation><affiliation>Address for correspondence: Dr. Sally E. Ford, Department of Pathology, Richardson Laboratory, RM 201, Queen's University, Kingston, Ontario. K7L 3N6; Tel: 613-533-2819; Fax: 613-533-2907</affiliation><affiliation>E-mail: ford@cliff.path.queensu.ca</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="research-article" displayLabel="Full-length article"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1999</dateIssued><copyrightDate encoding="w3cdtf">1999</copyrightDate></originInfo><language><languageTerm type="code" authority="iso639-2b">eng</languageTerm><languageTerm type="code" authority="rfc3066">en</languageTerm></language><physicalDescription><internetMediaType>text/html</internetMediaType></physicalDescription><abstract lang="en">Pathologists are dissuaded from the pathological study of the conduction system by the high cost and complexity of a traditional complete study. However, a simplified, low-cost approach can produce concrete information when performed in carefully selected cases of atrioventricular block, as demonstrated in the two cases of congenital cystic tumor of the atrioventricular node described in this report.</abstract><note type="content">Section title: Articles</note><note type="content">Figure 1: (A) The heart is opened to show the right atrium: the rectangle superimposed on the photograph represents the block of tissue removed. B shows the excised block of tissue, which was then sliced vertically. The far right portion of the block was discarded as being too far into the membranous septum. C shows the block cut into pieces, with one side inked to prevent examination of contiguous sections</note><note type="content">Figure 2: The normal position of the node in Case 1 is occupied by clefts and nests of tumor in a connective tissue matrix. The tumor extends into one of the strands of a coronary sinus web (W)</note><note type="content">Figure 3: The clefts are lined with cuboidal epithelioid cells (A), which stained positive for cytokeratin in Case 2 (B). This stain was positive in both cases, as was carcino-embryonic antigen</note><note type="content">Table 1: Histochemical and Immunohistochemical Characteristics of the Tumors</note><relatedItem type="host"><titleInfo><title>Cardiovascular Pathology</title></titleInfo><titleInfo type="abbreviated"><title>CVP</title></titleInfo><genre type="journal">journal</genre><originInfo><dateIssued encoding="w3cdtf">199907</dateIssued></originInfo><identifier type="ISSN">1054-8807</identifier><identifier type="PII">S1054-8807(00)X0026-9</identifier><part><date>199907</date><detail type="volume"><number>8</number><caption>vol.</caption></detail><detail type="issue"><number>4</number><caption>no.</caption></detail><extent unit="issue pages"><start>185</start><end>244</end></extent><extent unit="pages"><start>233</start><end>237</end></extent></part></relatedItem><identifier type="istex">E982768180B70E5FDB5F4AF47CCFABB5F8CC80F4</identifier><identifier type="DOI">10.1016/S1054-8807(99)00013-7</identifier><identifier type="PII">S1054-8807(99)00013-7</identifier><accessCondition type="use and reproduction" contentType="copyright">©1999 Elsevier Science Inc.</accessCondition><recordInfo><recordContentSource>ELSEVIER</recordContentSource><recordOrigin>Elsevier Science Inc., ©1999</recordOrigin></recordInfo></mods></metadata><serie></serie></istex></record>Pour manipuler ce document sous Unix (Dilib)
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