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- Publisher Website: 10.1159/000190301
- Scopus: eid_2-s2.0-0030660461
- PMID: 9375832
- WOS: WOS:A1997YD27700017
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Article: A characteristic dissection microscopy appearance of a renal biopsy of a Fabry heterozygote
Title | A characteristic dissection microscopy appearance of a renal biopsy of a Fabry heterozygote |
---|---|
Authors | |
Keywords | Dissection microscopy Fabry disease Renal biopsy |
Issue Date | 1997 |
Publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/NEF |
Citation | Nephron, 1997, v. 77 n. 3, p. 354-356 How to Cite? |
Abstract | We report a 15-year-old Fabry heterozygote presenting to us with asymptomatic proteinuria. During the dissection-microscopic examination, the glomeruli exhibited a characteristic swollen, glistening and white appearance. They were swollen and bulged out from the surface of the renal core. The glomerular tufts appeared to be filled with opaque and whitish material giving them a pale white discoloration. This appearance is due to the accumulation of glycosphingolipids in visceral epithelial cells of the kidney. This feature is important for the investigation of female patients with asymptomatic proteinuria, as in two thirds of Fabry heterozygotes the characteristic skin lesions are absent, and thus heterozygous Fabry disease may not be considered. We suggest that this easily demonstrable appearance can be the first evidence for the disease and pathologists should be aware of it in future. |
Persistent Identifier | http://hdl.handle.net/10722/148066 |
ISSN | 2023 SCImago Journal Rankings: 0.774 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yuen, NWF | en_US |
dc.contributor.author | Lam, CW | en_US |
dc.contributor.author | Chow, TC | en_US |
dc.contributor.author | Chiu, MC | en_US |
dc.date.accessioned | 2012-05-29T06:10:40Z | - |
dc.date.available | 2012-05-29T06:10:40Z | - |
dc.date.issued | 1997 | en_US |
dc.identifier.citation | Nephron, 1997, v. 77 n. 3, p. 354-356 | en_US |
dc.identifier.issn | 0028-2766 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/148066 | - |
dc.description.abstract | We report a 15-year-old Fabry heterozygote presenting to us with asymptomatic proteinuria. During the dissection-microscopic examination, the glomeruli exhibited a characteristic swollen, glistening and white appearance. They were swollen and bulged out from the surface of the renal core. The glomerular tufts appeared to be filled with opaque and whitish material giving them a pale white discoloration. This appearance is due to the accumulation of glycosphingolipids in visceral epithelial cells of the kidney. This feature is important for the investigation of female patients with asymptomatic proteinuria, as in two thirds of Fabry heterozygotes the characteristic skin lesions are absent, and thus heterozygous Fabry disease may not be considered. We suggest that this easily demonstrable appearance can be the first evidence for the disease and pathologists should be aware of it in future. | en_US |
dc.language | eng | en_US |
dc.publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/NEF | en_US |
dc.relation.ispartof | Nephron | en_US |
dc.subject | Dissection microscopy | - |
dc.subject | Fabry disease | - |
dc.subject | Renal biopsy | - |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Biopsy | en_US |
dc.subject.mesh | Epithelial Cells - Ultrastructure | en_US |
dc.subject.mesh | Fabry Disease - Complications - Genetics - Pathology | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Heterozygote | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Kidney Glomerulus - Pathology - Ultrastructure | en_US |
dc.subject.mesh | Microscopy, Electron, Scanning | en_US |
dc.subject.mesh | Proteinuria - Etiology | en_US |
dc.subject.mesh | Urine - Cytology | en_US |
dc.title | A characteristic dissection microscopy appearance of a renal biopsy of a Fabry heterozygote | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lam, CW:ching-wanlam@pathology.hku.hk | en_US |
dc.identifier.authority | Lam, CW=rp00260 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1159/000190301 | - |
dc.identifier.pmid | 9375832 | - |
dc.identifier.scopus | eid_2-s2.0-0030660461 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0030660461&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 77 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.spage | 354 | en_US |
dc.identifier.epage | 356 | en_US |
dc.identifier.isi | WOS:A1997YD27700017 | - |
dc.publisher.place | Switzerland | en_US |
dc.identifier.issnl | 0028-2766 | - |