Loading…
Immunotactoid glomerulopathy with fingerprint immune deposits: a variant of lupus nephritis?
Immunotactoid glomerulopathy is a distinct clinico-pathological entity which has recently been defined. The term immunotactoid refers to highly organized immune depositions appearing as rod-like microtubular structures in ultrastructural examination. We describe a patient with mixed connective tissu...
Saved in:
| Published in: | Virchows Archiv A Pathological Anatomy and Histopathology 1989, Vol.415 (2), p.181-186 |
|---|---|
| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Subjects: | |
| Citations: | Items that this one cites |
| Online Access: | Get full text |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| cited_by | |
|---|---|
| cites | cdi_FETCH-LOGICAL-c299t-367e4ad3ce594535f12d5b8a4055d60cf02aa0e705a65e023900b6c51389b93a3 |
| container_end_page | 186 |
| container_issue | 2 |
| container_start_page | 181 |
| container_title | Virchows Archiv A Pathological Anatomy and Histopathology |
| container_volume | 415 |
| creator | MAC-MOUNE LAI, F KAR NENG LAI LI, E. K JAO YIU SUNG TAM, J. S. L |
| description | Immunotactoid glomerulopathy is a distinct clinico-pathological entity which has recently been defined. The term immunotactoid refers to highly organized immune depositions appearing as rod-like microtubular structures in ultrastructural examination. We describe a patient with mixed connective tissue disease who demonstrates characteristic features of immunotactoid glomerulopathy. The diagnosis was made after excluding amyloidosis, cryoglobulinaemia and lupus nephritis. In addition to immunotactoid microtubules, ultrastructural examination also demonstrated presence of fingerprint depositions which were intimately mixed with immunotactoid structures. Fingerprint deposits have been described in lupus nephritis and cryoglobulin-related nephropathy, but rarely in other glomerulonephritis. These unique findings in our patient may suggest a previously unsuspected relationship between the syndrome of immunotactoid glomerulopathy and systemic lupus erythematosus. |
| doi_str_mv | 10.1007/bf00784357 |
| format | article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1007_BF00784357</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>79059643</sourcerecordid><originalsourceid>FETCH-LOGICAL-c299t-367e4ad3ce594535f12d5b8a4055d60cf02aa0e705a65e023900b6c51389b93a3</originalsourceid><addsrcrecordid>eNo9kM1LxDAQxYMo6_px8S7kIB6E6jRpmsaLqPgFghe9CWWapruRtqlJqvjf28V1LzOH95vHvEfIUQrnKYC8qJppFhkXcovM04yzhHGQ22QOqcwSyVWxS_ZC-AAQIi3EjMyYmC4kn5P3p64bexdRR2drumhdZ_zYugHj8od-27ikje0Xxg_e9pHaFW1obQYXbAyXFOkXeouT5BrajsMYaG-GpbfRhqsDstNgG8zheu-Tt_u719vH5Pnl4en2-jnRTKmY8FyaDGuujVCZ4KJJWS2qArPp3ToH3QBDBCNBYC4MMK4AqlyLlBeqUhz5Pjn98x28-xxNiGVngzZti71xYyilAqHyjE_g2R-ovQvBm6acYnXof8oUylWV5c39f5UTfLx2HavO1Bt03d2kn6x1DBrbxmOvbdhgkhUMWMZ_AdxDe7k</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>79059643</pqid></control><display><type>article</type><title>Immunotactoid glomerulopathy with fingerprint immune deposits: a variant of lupus nephritis?</title><source>SpringerLink Online Journals Archive Complete</source><creator>MAC-MOUNE LAI, F ; KAR NENG LAI ; LI, E. K ; JAO YIU SUNG ; TAM, J. S. L</creator><creatorcontrib>MAC-MOUNE LAI, F ; KAR NENG LAI ; LI, E. K ; JAO YIU SUNG ; TAM, J. S. L</creatorcontrib><description>Immunotactoid glomerulopathy is a distinct clinico-pathological entity which has recently been defined. The term immunotactoid refers to highly organized immune depositions appearing as rod-like microtubular structures in ultrastructural examination. We describe a patient with mixed connective tissue disease who demonstrates characteristic features of immunotactoid glomerulopathy. The diagnosis was made after excluding amyloidosis, cryoglobulinaemia and lupus nephritis. In addition to immunotactoid microtubules, ultrastructural examination also demonstrated presence of fingerprint depositions which were intimately mixed with immunotactoid structures. Fingerprint deposits have been described in lupus nephritis and cryoglobulin-related nephropathy, but rarely in other glomerulonephritis. These unique findings in our patient may suggest a previously unsuspected relationship between the syndrome of immunotactoid glomerulopathy and systemic lupus erythematosus.</description><identifier>ISSN: 0174-7398</identifier><identifier>EISSN: 1432-2307</identifier><identifier>DOI: 10.1007/bf00784357</identifier><identifier>PMID: 2500773</identifier><identifier>CODEN: VAAHDJ</identifier><language>eng</language><publisher>Heidelberg: Springer</publisher><subject>Adult ; Biological and medical sciences ; Crystallization ; Female ; Fluorescent Antibody Technique ; Glomerulonephritis ; Humans ; Kidney Glomerulus - immunology ; Kidney Glomerulus - ultrastructure ; Lupus Erythematosus, Systemic - immunology ; Lupus Erythematosus, Systemic - pathology ; Lupus Nephritis - immunology ; Lupus Nephritis - pathology ; Medical sciences ; Microscopy, Electron ; Microscopy, Fluorescence ; Microtubules - ultrastructure ; Mixed Connective Tissue Disease - immunology ; Mixed Connective Tissue Disease - pathology ; Nephrology. Urinary tract diseases ; Nephropathies. Renovascular diseases. Renal failure ; Nephrotic Syndrome - classification ; Nephrotic Syndrome - immunology ; Nephrotic Syndrome - pathology</subject><ispartof>Virchows Archiv A Pathological Anatomy and Histopathology, 1989, Vol.415 (2), p.181-186</ispartof><rights>1989 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c299t-367e4ad3ce594535f12d5b8a4055d60cf02aa0e705a65e023900b6c51389b93a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7282024$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2500773$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>MAC-MOUNE LAI, F</creatorcontrib><creatorcontrib>KAR NENG LAI</creatorcontrib><creatorcontrib>LI, E. K</creatorcontrib><creatorcontrib>JAO YIU SUNG</creatorcontrib><creatorcontrib>TAM, J. S. L</creatorcontrib><title>Immunotactoid glomerulopathy with fingerprint immune deposits: a variant of lupus nephritis?</title><title>Virchows Archiv A Pathological Anatomy and Histopathology</title><addtitle>Virchows Arch A Pathol Anat Histopathol</addtitle><description>Immunotactoid glomerulopathy is a distinct clinico-pathological entity which has recently been defined. The term immunotactoid refers to highly organized immune depositions appearing as rod-like microtubular structures in ultrastructural examination. We describe a patient with mixed connective tissue disease who demonstrates characteristic features of immunotactoid glomerulopathy. The diagnosis was made after excluding amyloidosis, cryoglobulinaemia and lupus nephritis. In addition to immunotactoid microtubules, ultrastructural examination also demonstrated presence of fingerprint depositions which were intimately mixed with immunotactoid structures. Fingerprint deposits have been described in lupus nephritis and cryoglobulin-related nephropathy, but rarely in other glomerulonephritis. These unique findings in our patient may suggest a previously unsuspected relationship between the syndrome of immunotactoid glomerulopathy and systemic lupus erythematosus.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Crystallization</subject><subject>Female</subject><subject>Fluorescent Antibody Technique</subject><subject>Glomerulonephritis</subject><subject>Humans</subject><subject>Kidney Glomerulus - immunology</subject><subject>Kidney Glomerulus - ultrastructure</subject><subject>Lupus Erythematosus, Systemic - immunology</subject><subject>Lupus Erythematosus, Systemic - pathology</subject><subject>Lupus Nephritis - immunology</subject><subject>Lupus Nephritis - pathology</subject><subject>Medical sciences</subject><subject>Microscopy, Electron</subject><subject>Microscopy, Fluorescence</subject><subject>Microtubules - ultrastructure</subject><subject>Mixed Connective Tissue Disease - immunology</subject><subject>Mixed Connective Tissue Disease - pathology</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Nephropathies. Renovascular diseases. Renal failure</subject><subject>Nephrotic Syndrome - classification</subject><subject>Nephrotic Syndrome - immunology</subject><subject>Nephrotic Syndrome - pathology</subject><issn>0174-7398</issn><issn>1432-2307</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNo9kM1LxDAQxYMo6_px8S7kIB6E6jRpmsaLqPgFghe9CWWapruRtqlJqvjf28V1LzOH95vHvEfIUQrnKYC8qJppFhkXcovM04yzhHGQ22QOqcwSyVWxS_ZC-AAQIi3EjMyYmC4kn5P3p64bexdRR2drumhdZ_zYugHj8od-27ikje0Xxg_e9pHaFW1obQYXbAyXFOkXeouT5BrajsMYaG-GpbfRhqsDstNgG8zheu-Tt_u719vH5Pnl4en2-jnRTKmY8FyaDGuujVCZ4KJJWS2qArPp3ToH3QBDBCNBYC4MMK4AqlyLlBeqUhz5Pjn98x28-xxNiGVngzZti71xYyilAqHyjE_g2R-ovQvBm6acYnXof8oUylWV5c39f5UTfLx2HavO1Bt03d2kn6x1DBrbxmOvbdhgkhUMWMZ_AdxDe7k</recordid><startdate>1989</startdate><enddate>1989</enddate><creator>MAC-MOUNE LAI, F</creator><creator>KAR NENG LAI</creator><creator>LI, E. K</creator><creator>JAO YIU SUNG</creator><creator>TAM, J. S. L</creator><general>Springer</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>1989</creationdate><title>Immunotactoid glomerulopathy with fingerprint immune deposits: a variant of lupus nephritis?</title><author>MAC-MOUNE LAI, F ; KAR NENG LAI ; LI, E. K ; JAO YIU SUNG ; TAM, J. S. L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c299t-367e4ad3ce594535f12d5b8a4055d60cf02aa0e705a65e023900b6c51389b93a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Crystallization</topic><topic>Female</topic><topic>Fluorescent Antibody Technique</topic><topic>Glomerulonephritis</topic><topic>Humans</topic><topic>Kidney Glomerulus - immunology</topic><topic>Kidney Glomerulus - ultrastructure</topic><topic>Lupus Erythematosus, Systemic - immunology</topic><topic>Lupus Erythematosus, Systemic - pathology</topic><topic>Lupus Nephritis - immunology</topic><topic>Lupus Nephritis - pathology</topic><topic>Medical sciences</topic><topic>Microscopy, Electron</topic><topic>Microscopy, Fluorescence</topic><topic>Microtubules - ultrastructure</topic><topic>Mixed Connective Tissue Disease - immunology</topic><topic>Mixed Connective Tissue Disease - pathology</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Nephropathies. Renovascular diseases. Renal failure</topic><topic>Nephrotic Syndrome - classification</topic><topic>Nephrotic Syndrome - immunology</topic><topic>Nephrotic Syndrome - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>MAC-MOUNE LAI, F</creatorcontrib><creatorcontrib>KAR NENG LAI</creatorcontrib><creatorcontrib>LI, E. K</creatorcontrib><creatorcontrib>JAO YIU SUNG</creatorcontrib><creatorcontrib>TAM, J. S. L</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Virchows Archiv A Pathological Anatomy and Histopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>MAC-MOUNE LAI, F</au><au>KAR NENG LAI</au><au>LI, E. K</au><au>JAO YIU SUNG</au><au>TAM, J. S. L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunotactoid glomerulopathy with fingerprint immune deposits: a variant of lupus nephritis?</atitle><jtitle>Virchows Archiv A Pathological Anatomy and Histopathology</jtitle><addtitle>Virchows Arch A Pathol Anat Histopathol</addtitle><date>1989</date><risdate>1989</risdate><volume>415</volume><issue>2</issue><spage>181</spage><epage>186</epage><pages>181-186</pages><issn>0174-7398</issn><eissn>1432-2307</eissn><coden>VAAHDJ</coden><abstract>Immunotactoid glomerulopathy is a distinct clinico-pathological entity which has recently been defined. The term immunotactoid refers to highly organized immune depositions appearing as rod-like microtubular structures in ultrastructural examination. We describe a patient with mixed connective tissue disease who demonstrates characteristic features of immunotactoid glomerulopathy. The diagnosis was made after excluding amyloidosis, cryoglobulinaemia and lupus nephritis. In addition to immunotactoid microtubules, ultrastructural examination also demonstrated presence of fingerprint depositions which were intimately mixed with immunotactoid structures. Fingerprint deposits have been described in lupus nephritis and cryoglobulin-related nephropathy, but rarely in other glomerulonephritis. These unique findings in our patient may suggest a previously unsuspected relationship between the syndrome of immunotactoid glomerulopathy and systemic lupus erythematosus.</abstract><cop>Heidelberg</cop><cop>Berlin</cop><pub>Springer</pub><pmid>2500773</pmid><doi>10.1007/bf00784357</doi><tpages>6</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0174-7398 |
| ispartof | Virchows Archiv A Pathological Anatomy and Histopathology, 1989, Vol.415 (2), p.181-186 |
| issn | 0174-7398 1432-2307 |
| language | eng |
| recordid | cdi_crossref_primary_10_1007_BF00784357 |
| source | SpringerLink Online Journals Archive Complete |
| subjects | Adult Biological and medical sciences Crystallization Female Fluorescent Antibody Technique Glomerulonephritis Humans Kidney Glomerulus - immunology Kidney Glomerulus - ultrastructure Lupus Erythematosus, Systemic - immunology Lupus Erythematosus, Systemic - pathology Lupus Nephritis - immunology Lupus Nephritis - pathology Medical sciences Microscopy, Electron Microscopy, Fluorescence Microtubules - ultrastructure Mixed Connective Tissue Disease - immunology Mixed Connective Tissue Disease - pathology Nephrology. Urinary tract diseases Nephropathies. Renovascular diseases. Renal failure Nephrotic Syndrome - classification Nephrotic Syndrome - immunology Nephrotic Syndrome - pathology |
| title | Immunotactoid glomerulopathy with fingerprint immune deposits: a variant of lupus nephritis? |
| url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T08%3A20%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Immunotactoid%20glomerulopathy%20with%20fingerprint%20immune%20deposits:%20a%20variant%20of%20lupus%20nephritis?&rft.jtitle=Virchows%20Archiv%20A%20Pathological%20Anatomy%20and%20Histopathology&rft.au=MAC-MOUNE%20LAI,%20F&rft.date=1989&rft.volume=415&rft.issue=2&rft.spage=181&rft.epage=186&rft.pages=181-186&rft.issn=0174-7398&rft.eissn=1432-2307&rft.coden=VAAHDJ&rft_id=info:doi/10.1007/bf00784357&rft_dat=%3Cproquest_cross%3E79059643%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c299t-367e4ad3ce594535f12d5b8a4055d60cf02aa0e705a65e023900b6c51389b93a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=79059643&rft_id=info:pmid/2500773&rfr_iscdi=true |