A chronological study of the histopathology of filarial disease in cats and dogs caused by Brugia pahangi (Buckley and Edeson, 1956)
Identifieur interne : 004096 ( Istex/Corpus ); précédent : 004095; suivant : 004097A chronological study of the histopathology of filarial disease in cats and dogs caused by Brugia pahangi (Buckley and Edeson, 1956)
Auteurs : John F. Schacher ; Philip F. SahyounSource :
- Transactions of the Royal Society of Tropical Medicine and Hygiene [ 0035-9203 ] ; 1967.
Abstract
Brugia pahangi infections in the lymph nodes of cats have been studied in serial sections stained with H & E at intervals of from 3 days to 16 1 2 months; material from a few dogs was also examined. The pathological changes are described and discussed in relation to the life cycle of the agent. Reactions were found to: living and dead larvae (third and fourth stage); moulting fluids and moulted cuticles of the third and fourth moults; uterine secretions, infertile eggs and microfilariae; and finally to living and dead adult worms. Pathological changes in dogs are strikingly more rapid and extreme than in cats. Basic causal mechanisms underlying some features of filarial disease are discussed in relation to the filarial life cycle, the lesions produced by worms and their products, the pattern of lymphatic drainage, and the functional physiology of the lymphatic system.
Url:
DOI: 10.1016/0035-9203(67)90162-9
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The pathological changes are described and discussed in relation to the life cycle of the agent. Reactions were found to: living and dead larvae (third and fourth stage); moulting fluids and moulted cuticles of the third and fourth moults; uterine secretions, infertile eggs and microfilariae; and finally to living and dead adult worms. Pathological changes in dogs are strikingly more rapid and extreme than in cats. Basic causal mechanisms underlying some features of filarial disease are discussed in relation to the filarial life cycle, the lesions produced by worms and their products, the pattern of lymphatic drainage, and the functional physiology of the lymphatic system.</div></front></TEI><istex><corpusName>elsevier</corpusName><keywords><teeft><json:string>node</json:string><json:string>lymphatic</json:string><json:string>larva</json:string><json:string>lymphatics</json:string><json:string>moult</json:string><json:string>moulting</json:string><json:string>pahangi</json:string><json:string>filarial</json:string><json:string>peripheral sinus</json:string><json:string>afferent lymphatics</json:string><json:string>elephantiasis</json:string><json:string>schacher</json:string><json:string>thrombus</json:string><json:string>malayi</json:string><json:string>afferent</json:string><json:string>lymph nodes</json:string><json:string>cuticle</json:string><json:string>vascularization</json:string><json:string>lymphangiectasis</json:string><json:string>edeson</json:string><json:string>sinus</json:string><json:string>thrombolymphangitis</json:string><json:string>afferent lymphatic</json:string><json:string>microfilariae</json:string><json:string>lymphoid</json:string><json:string>lymph</json:string><json:string>histopathology</json:string><json:string>filariasis</json:string><json:string>lymphatic system</json:string><json:string>parasit</json:string><json:string>moulting fluids</json:string><json:string>polypoid</json:string><json:string>life cycle</json:string><json:string>filarial disease</json:string><json:string>lesion</json:string><json:string>present study</json:string><json:string>parasite</json:string><json:string>pathological changes</json:string><json:string>lymph node</json:string><json:string>lymph flow</json:string><json:string>sheath reaction</json:string><json:string>stage larvae</json:string><json:string>third moult</json:string><json:string>polypoid thrombolymphangitis</json:string><json:string>hyperplasia</json:string><json:string>sheath</json:string><json:string>hyalinization</json:string><json:string>mild lymphangiectasis</json:string><json:string>fourth stage</json:string><json:string>popliteal node</json:string><json:string>medullary oedema</json:string><json:string>diffuse fibrosis</json:string><json:string>blood vessels</json:string><json:string>final host</json:string><json:string>cast sheath</json:string><json:string>worm</json:string><json:string>dead parasites</json:string><json:string>moulting fluid</json:string><json:string>lymphoid elements</json:string><json:string>epithelioid pattern</json:string><json:string>queen hatshepsut</json:string><json:string>third stage</json:string><json:string>cortical sinus</json:string><json:string>moulting process</json:string><json:string>sheath material</json:string><json:string>brugia pahangi</json:string><json:string>adult worms</json:string><json:string>funerary temple</json:string><json:string>immature adult</json:string><json:string>plasma cells</json:string><json:string>secondary lymph follicles</json:string><json:string>pahangi infections</json:string><json:string>final moult</json:string><json:string>littoral cells</json:string><json:string>lymphatic obstruction</json:string><json:string>malayi infections</json:string><json:string>cryptic filariasis</json:string><json:string>parietal lymphangitis</json:string><json:string>dead larvae</json:string><json:string>foreign body giant cells</json:string><json:string>exsheathing fluids</json:string><json:string>lymph stasis</json:string><json:string>lymphatic trunks</json:string><json:string>benninghoffand herman</json:string><json:string>serial sections</json:string><json:string>mucoid material</json:string><json:string>lower uterus</json:string><json:string>infertile eggs</json:string><json:string>uterine mucus</json:string><json:string>acute damage</json:string><json:string>stage cuticle</json:string><json:string>dead adult worms</json:string><json:string>lymph drainage</json:string><json:string>lymphatic drainage</json:string><json:string>tropical diseases</json:string><json:string>lymphoid tissue</json:string><json:string>harvard univ</json:string><json:string>adipose tissue</json:string></teeft></keywords><author><json:item><name>John F. 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It was initiated under the sponsorship of a grant from the Commission on Parasitic Diseases, Armed Forces Epidemiological Board to Dr. Paul C. Beaver, supported in part by the Office of the Surgeon General, Department of the Army.</note><note type="content">Section title: Communication</note></notesStmt><sourceDesc><biblStruct type="inbook"><analytic><title level="a">A chronological study of the histopathology of filarial disease in cats and dogs caused by Brugia pahangi (Buckley and Edeson, 1956)</title><author xml:id="author-0000"><persName><forename type="first">John F.</forename><surname>Schacher</surname></persName><affiliation>Departments of Tropical Health and Pathology, Faculty of Medical Sciences, American University of Beirut, Beirut, Lebanon</affiliation></author><author xml:id="author-0001"><persName><forename type="first">Philip F.</forename><surname>Sahyoun</surname></persName><affiliation>Departments of Tropical Health and Pathology, Faculty of Medical Sciences, American University of Beirut, Beirut, Lebanon</affiliation></author><idno type="istex">89A81C57D04A20BD90C6EC1D99682D946F596CF2</idno><idno type="DOI">10.1016/0035-9203(67)90162-9</idno><idno type="PII">0035-9203(67)90162-9</idno></analytic><monogr><title level="j">Transactions of the Royal Society of Tropical Medicine and Hygiene</title><title level="j" type="abbrev">TRSTMH</title><idno type="pISSN">0035-9203</idno><idno type="PII">S0035-9203(00)X0288-X</idno><imprint><publisher>ELSEVIER</publisher><date type="published" when="1967"></date><biblScope unit="volume">61</biblScope><biblScope unit="issue">2</biblScope><biblScope unit="page" from="234">234</biblScope><biblScope unit="page" to="236">236</biblScope></imprint></monogr></biblStruct></sourceDesc></fileDesc><profileDesc><creation><date>1967</date></creation><langUsage><language ident="en">en</language></langUsage><abstract xml:lang="en"><p>Brugia pahangi infections in the lymph nodes of cats have been studied in serial sections stained with H & E at intervals of from 3 days to 16 1 2 months; material from a few dogs was also examined. The pathological changes are described and discussed in relation to the life cycle of the agent. Reactions were found to: living and dead larvae (third and fourth stage); moulting fluids and moulted cuticles of the third and fourth moults; uterine secretions, infertile eggs and microfilariae; and finally to living and dead adult worms. Pathological changes in dogs are strikingly more rapid and extreme than in cats. Basic causal mechanisms underlying some features of filarial disease are discussed in relation to the filarial life cycle, the lesions produced by worms and their products, the pattern of lymphatic drainage, and the functional physiology of the lymphatic system.</p></abstract></profileDesc><revisionDesc><change when="1967">Published</change></revisionDesc></teiHeader></istex:fulltextTEI><json:item><extension>txt</extension><original>false</original><mimetype>text/plain</mimetype><uri>https://api.istex.fr/document/89A81C57D04A20BD90C6EC1D99682D946F596CF2/fulltext/txt</uri></json:item></fulltext><metadata><istex:metadataXml wicri:clean="Elsevier, elements deleted: tail"><istex:xmlDeclaration>version="1.0" encoding="utf-8"</istex:xmlDeclaration><istex:docType PUBLIC="-//ES//DTD journal article DTD version 4.5.2//EN//XML" URI="art452.dtd" name="istex:docType"></istex:docType><istex:document><converted-article version="4.5.2" docsubtype="sco"><item-info><jid>TRSTMH</jid><aid>67901629</aid><ce:pii>0035-9203(67)90162-9</ce:pii><ce:doi>10.1016/0035-9203(67)90162-9</ce:doi><ce:copyright type="unknown" year="1967"></ce:copyright></item-info><head><ce:article-footnote><ce:label>☆</ce:label><ce:note-para>This investigation was supported in part by Public Health Service Research Grant AI-05195 from the Institutes of Allergy and Infectious Diseases, U.S. Department of Health, Education and Welfare. It was initiated under the sponsorship of a grant from the Commission on Parasitic Diseases, Armed Forces Epidemiological Board to Dr. Paul C. Beaver, supported in part by the Office of the Surgeon General, Department of the Army.</ce:note-para></ce:article-footnote><ce:dochead><ce:textfn>Communication</ce:textfn></ce:dochead><ce:title>A chronological study of the histopathology of filarial disease in cats and dogs caused by <ce:italic>Brugia pahangi</ce:italic> (Buckley and Edeson, 1956)</ce:title><ce:author-group><ce:author><ce:given-name>John F.</ce:given-name><ce:surname>Schacher</ce:surname></ce:author><ce:author><ce:given-name>Philip F.</ce:given-name><ce:surname>Sahyoun</ce:surname></ce:author><ce:affiliation><ce:textfn>Departments of Tropical Health and Pathology, Faculty of Medical Sciences, American University of Beirut, Beirut, Lebanon</ce:textfn></ce:affiliation></ce:author-group><ce:abstract><ce:section-title>Abstract</ce:section-title><ce:abstract-sec><ce:simple-para><ce:italic>Brugia pahangi</ce:italic> infections in the lymph nodes of cats have been studied in serial sections stained with H & E at intervals of from 3 days to 16<math altimg="si1.gif"><fr shape="case"><nu>1</nu><de>2</de></fr></math> months; material from a few dogs was also examined.</ce:simple-para><ce:simple-para>The pathological changes are described and discussed in relation to the life cycle of the agent. Reactions were found to: living and dead larvae (third and fourth stage); moulting fluids and moulted cuticles of the third and fourth moults; uterine secretions, infertile eggs and microfilariae; and finally to living and dead adult worms. Pathological changes in dogs are strikingly more rapid and extreme than in cats.</ce:simple-para><ce:simple-para>Basic causal mechanisms underlying some features of filarial disease are discussed in relation to the filarial life cycle, the lesions produced by worms and their products, the pattern of lymphatic drainage, and the functional physiology of the lymphatic system.</ce:simple-para></ce:abstract-sec></ce:abstract></head></converted-article></istex:document></istex:metadataXml><mods version="3.6"><titleInfo><title>A chronological study of the histopathology of filarial disease in cats and dogs caused by Brugia pahangi (Buckley and Edeson, 1956)</title></titleInfo><titleInfo type="alternative" contentType="CDATA"><title>A chronological study of the histopathology of filarial disease in cats and dogs caused by</title></titleInfo><name type="personal"><namePart type="given">John F.</namePart><namePart type="family">Schacher</namePart><affiliation>Departments of Tropical Health and Pathology, Faculty of Medical Sciences, American University of Beirut, Beirut, Lebanon</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Philip F.</namePart><namePart type="family">Sahyoun</namePart><affiliation>Departments of Tropical Health and Pathology, Faculty of Medical Sciences, American University of Beirut, Beirut, Lebanon</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="brief-communication" displayLabel="Short communication"></genre><originInfo><publisher>ELSEVIER</publisher><dateIssued encoding="w3cdtf">1967</dateIssued><copyrightDate encoding="w3cdtf">1967</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">Brugia pahangi infections in the lymph nodes of cats have been studied in serial sections stained with H & E at intervals of from 3 days to 16 1 2 months; material from a few dogs was also examined. The pathological changes are described and discussed in relation to the life cycle of the agent. Reactions were found to: living and dead larvae (third and fourth stage); moulting fluids and moulted cuticles of the third and fourth moults; uterine secretions, infertile eggs and microfilariae; and finally to living and dead adult worms. Pathological changes in dogs are strikingly more rapid and extreme than in cats. Basic causal mechanisms underlying some features of filarial disease are discussed in relation to the filarial life cycle, the lesions produced by worms and their products, the pattern of lymphatic drainage, and the functional physiology of the lymphatic system.</abstract><note>This investigation was supported in part by Public Health Service Research Grant AI-05195 from the Institutes of Allergy and Infectious Diseases, U.S. Department of Health, Education and Welfare. It was initiated under the sponsorship of a grant from the Commission on Parasitic Diseases, Armed Forces Epidemiological Board to Dr. Paul C. 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