Porphyria and pseudo-porphyria in hemodialyzed patients
A case of “bullous dermatosis of hemodialysis” which turns out to be a true hereditary PCT, is presented. The particularly serious and fast course of the cutaneous lesions might be due to the extremely high level of plasmatic porphyrins, which neither the residual renal function nor the hemodialysis...
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| Veröffentlicht in: | International journal of biochemistry 1980, Vol.12 (5), p.963-967 |
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| container_end_page | 967 |
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| container_issue | 5 |
| container_start_page | 963 |
| container_title | International journal of biochemistry |
| container_volume | 12 |
| creator | Topi, G.C. Gandolfo, L.D'alessandro De Costanza, F. Cancarini, G.C. |
| description | A case of “bullous dermatosis of hemodialysis” which turns out to be a true hereditary PCT, is presented. The particularly serious and fast course of the cutaneous lesions might be due to the extremely high level of plasmatic porphyrins, which neither the residual renal function nor the hemodialysis are able to reduce. |
| doi_str_mv | 10.1016/0020-711X(80)90193-7 |
| format | Article |
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The particularly serious and fast course of the cutaneous lesions might be due to the extremely high level of plasmatic porphyrins, which neither the residual renal function nor the hemodialysis are able to reduce.</description><subject>Female</subject><subject>Humans</subject><subject>Kidney Failure, Chronic - complications</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Pedigree</subject><subject>Porphyrias - complications</subject><subject>Porphyrias - etiology</subject><subject>Porphyrias - genetics</subject><subject>Porphyrins - metabolism</subject><subject>Renal Dialysis - adverse effects</subject><subject>Skin Diseases - complications</subject><subject>Skin Diseases - etiology</subject><subject>Skin Diseases - genetics</subject><issn>0020-711X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1980</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LxDAQhnNQ1rX6DxT2JHqoTtpk01wEWfyCBT0oeAtpMmUjbVOTVlh_vV132aOngfdjhnkIOaNwTYHObwAySAWlH5cFXEmgMk_FAZnu5SNyHOMnjEbB6IRMBONAuZgS8epDt1oHp2e6tbMu4mB92u1F185W2HjrdL3-wTGge4dtH0_IYaXriKe7mZD3h_u3xVO6fHl8XtwtU5Nz0adGaiskY5nllENZybwUIpOcZhUaRksrgXM7F0JAzi1oVpZ8numcVhYZK4s8IRfbvV3wXwPGXjUuGqxr3aIfohI8lyDHfxPCtkETfIwBK9UF1-iwVhTUhpHawFAbGKoA9cdIibF2vts_lA3afWkHaPRvtz6OT347DCqaEYBB6wKaXlnv_j_wCzGQd5Q</recordid><startdate>1980</startdate><enddate>1980</enddate><creator>Topi, G.C.</creator><creator>Gandolfo, L.D'alessandro</creator><creator>De Costanza, F.</creator><creator>Cancarini, G.C.</creator><general>Elsevier B.V</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>7X8</scope></search><sort><creationdate>1980</creationdate><title>Porphyria and pseudo-porphyria in hemodialyzed patients</title><author>Topi, G.C. ; Gandolfo, L.D'alessandro ; De Costanza, F. ; Cancarini, G.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-c9ad79442d5150bf93b7729512fec41bd9055d6777035d0a4bb562a31fde44b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1980</creationdate><topic>Female</topic><topic>Humans</topic><topic>Kidney Failure, Chronic - complications</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Pedigree</topic><topic>Porphyrias - complications</topic><topic>Porphyrias - etiology</topic><topic>Porphyrias - genetics</topic><topic>Porphyrins - metabolism</topic><topic>Renal Dialysis - adverse effects</topic><topic>Skin Diseases - complications</topic><topic>Skin Diseases - etiology</topic><topic>Skin Diseases - genetics</topic><toplevel>online_resources</toplevel><creatorcontrib>Topi, G.C.</creatorcontrib><creatorcontrib>Gandolfo, L.D'alessandro</creatorcontrib><creatorcontrib>De Costanza, F.</creatorcontrib><creatorcontrib>Cancarini, G.C.</creatorcontrib><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>International journal of biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Topi, G.C.</au><au>Gandolfo, L.D'alessandro</au><au>De Costanza, F.</au><au>Cancarini, G.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Porphyria and pseudo-porphyria in hemodialyzed patients</atitle><jtitle>International journal of biochemistry</jtitle><addtitle>Int J Biochem</addtitle><date>1980</date><risdate>1980</risdate><volume>12</volume><issue>5</issue><spage>963</spage><epage>967</epage><pages>963-967</pages><issn>0020-711X</issn><abstract>A case of “bullous dermatosis of hemodialysis” which turns out to be a true hereditary PCT, is presented. 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| ispartof | International journal of biochemistry, 1980, Vol.12 (5), p.963-967 |
| issn | 0020-711X |
| language | eng |
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| source | MEDLINE; Alma/SFX Local Collection |
| subjects | Female Humans Kidney Failure, Chronic - complications Kidney Failure, Chronic - therapy Male Middle Aged Pedigree Porphyrias - complications Porphyrias - etiology Porphyrias - genetics Porphyrins - metabolism Renal Dialysis - adverse effects Skin Diseases - complications Skin Diseases - etiology Skin Diseases - genetics |
| title | Porphyria and pseudo-porphyria in hemodialyzed patients |
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