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Identification and treatment of late onset Fanconi's anemia
Cytogenetic Unit, Elena d'Aosta Hospital, Naples, Italy. We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a small Southern Italian town. The patient was pancytopenic when she was 31, and was found to be aplastic at the age of 34. Spontaneou...
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Published in: | Haematologica (Roma) 1995-11, Vol.80 (6), p.535-538 |
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creator | Zatterale, A Calzone, R Renda, S Catalano, L Selleri, C Notaro, R Rotoli, B |
description | Cytogenetic Unit, Elena d'Aosta Hospital, Naples, Italy.
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a small Southern Italian town. The patient was pancytopenic when she was 31, and was found to be aplastic at the age of 34. Spontaneous chromosomal breakages were not evident in peripheral blood lymphocyte cultures but the diepoxybutane (DEB) test, carried out during the aplastic phase, was clearly positive. Danazol treatment significantly improved her hematological condition, yielding a Hb peak value of 13.4 g/dL. Four years later moderate pancytopenia has recurred. This case demonstrates that even adult pancytopenic patients may have FA and that a test detecting chromosomal hypersensitivity to cross-linking agents is the only key to a correct diagnosis, which in turn is essential to avoid improper treatment. |
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We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a small Southern Italian town. The patient was pancytopenic when she was 31, and was found to be aplastic at the age of 34. Spontaneous chromosomal breakages were not evident in peripheral blood lymphocyte cultures but the diepoxybutane (DEB) test, carried out during the aplastic phase, was clearly positive. Danazol treatment significantly improved her hematological condition, yielding a Hb peak value of 13.4 g/dL. Four years later moderate pancytopenia has recurred. This case demonstrates that even adult pancytopenic patients may have FA and that a test detecting chromosomal hypersensitivity to cross-linking agents is the only key to a correct diagnosis, which in turn is essential to avoid improper treatment.</description><identifier>ISSN: 0390-6078</identifier><identifier>EISSN: 1592-8721</identifier><identifier>PMID: 8647521</identifier><language>eng</language><publisher>Pavia: Haematologica</publisher><subject>Adult ; Age of Onset ; Biological and medical sciences ; Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) ; Danazol - therapeutic use ; Fanconi Anemia - diagnosis ; Fanconi Anemia - drug therapy ; Female ; Humans ; Medical genetics ; Medical sciences</subject><ispartof>Haematologica (Roma), 1995-11, Vol.80 (6), p.535-538</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2946018$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8647521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zatterale, A</creatorcontrib><creatorcontrib>Calzone, R</creatorcontrib><creatorcontrib>Renda, S</creatorcontrib><creatorcontrib>Catalano, L</creatorcontrib><creatorcontrib>Selleri, C</creatorcontrib><creatorcontrib>Notaro, R</creatorcontrib><creatorcontrib>Rotoli, B</creatorcontrib><title>Identification and treatment of late onset Fanconi's anemia</title><title>Haematologica (Roma)</title><addtitle>Haematologica</addtitle><description>Cytogenetic Unit, Elena d'Aosta Hospital, Naples, Italy.
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a small Southern Italian town. The patient was pancytopenic when she was 31, and was found to be aplastic at the age of 34. Spontaneous chromosomal breakages were not evident in peripheral blood lymphocyte cultures but the diepoxybutane (DEB) test, carried out during the aplastic phase, was clearly positive. Danazol treatment significantly improved her hematological condition, yielding a Hb peak value of 13.4 g/dL. Four years later moderate pancytopenia has recurred. This case demonstrates that even adult pancytopenic patients may have FA and that a test detecting chromosomal hypersensitivity to cross-linking agents is the only key to a correct diagnosis, which in turn is essential to avoid improper treatment.</description><subject>Adult</subject><subject>Age of Onset</subject><subject>Biological and medical sciences</subject><subject>Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)</subject><subject>Danazol - therapeutic use</subject><subject>Fanconi Anemia - diagnosis</subject><subject>Fanconi Anemia - drug therapy</subject><subject>Female</subject><subject>Humans</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><issn>0390-6078</issn><issn>1592-8721</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1995</creationdate><recordtype>article</recordtype><recordid>eNo9z01LAzEQBuAgSq3VnyDswY_TQpLdTBI8SbFaKHjRc0iyiY3sR92kLP57A108Dcw8vMx7hpaESVoKTsk5WuJK4hIwF5foKsZvjCmWki_QQkDNGSVL9LRtXJ-CD1anMPSF7psijU6nLq-LwRetTq4Y-uhSsdG9HfrwGLNyXdDX6MLrNrqbea7Q5-blY_1W7t5ft-vnXbmnwFIpQTJjZAXSmgaE5sxjbCQHSyj3EkxtmAcmCa1BNlYI76gFMKIylABvqhV6OOUexuHn6GJSXYjWtW1-YzhGxbkAzgTO8HaGR9O5Rh3G0OnxV81t8_1uvutodevHXCjEf0ZlDZiIzO5PbB--9lMYnYqdbtscStU0TQIrUKxi1R-4d2oX</recordid><startdate>19951101</startdate><enddate>19951101</enddate><creator>Zatterale, A</creator><creator>Calzone, R</creator><creator>Renda, S</creator><creator>Catalano, L</creator><creator>Selleri, C</creator><creator>Notaro, R</creator><creator>Rotoli, B</creator><general>Haematologica</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19951101</creationdate><title>Identification and treatment of late onset Fanconi's anemia</title><author>Zatterale, A ; Calzone, R ; Renda, S ; Catalano, L ; Selleri, C ; Notaro, R ; Rotoli, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h265t-9695bb9369cbd68a75f00b976c127f96b4b5f65912469dc88fe2c66b83b2167d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1995</creationdate><topic>Adult</topic><topic>Age of Onset</topic><topic>Biological and medical sciences</topic><topic>Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)</topic><topic>Danazol - therapeutic use</topic><topic>Fanconi Anemia - diagnosis</topic><topic>Fanconi Anemia - drug therapy</topic><topic>Female</topic><topic>Humans</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zatterale, A</creatorcontrib><creatorcontrib>Calzone, R</creatorcontrib><creatorcontrib>Renda, S</creatorcontrib><creatorcontrib>Catalano, L</creatorcontrib><creatorcontrib>Selleri, C</creatorcontrib><creatorcontrib>Notaro, R</creatorcontrib><creatorcontrib>Rotoli, B</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>MEDLINE - Academic</collection><jtitle>Haematologica (Roma)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zatterale, A</au><au>Calzone, R</au><au>Renda, S</au><au>Catalano, L</au><au>Selleri, C</au><au>Notaro, R</au><au>Rotoli, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and treatment of late onset Fanconi's anemia</atitle><jtitle>Haematologica (Roma)</jtitle><addtitle>Haematologica</addtitle><date>1995-11-01</date><risdate>1995</risdate><volume>80</volume><issue>6</issue><spage>535</spage><epage>538</epage><pages>535-538</pages><issn>0390-6078</issn><eissn>1592-8721</eissn><abstract>Cytogenetic Unit, Elena d'Aosta Hospital, Naples, Italy.
We diagnosed Fanconi's anemia (FA) in a 34-year-old lady, daughter of consanguineous parents, from a small Southern Italian town. The patient was pancytopenic when she was 31, and was found to be aplastic at the age of 34. Spontaneous chromosomal breakages were not evident in peripheral blood lymphocyte cultures but the diepoxybutane (DEB) test, carried out during the aplastic phase, was clearly positive. Danazol treatment significantly improved her hematological condition, yielding a Hb peak value of 13.4 g/dL. Four years later moderate pancytopenia has recurred. This case demonstrates that even adult pancytopenic patients may have FA and that a test detecting chromosomal hypersensitivity to cross-linking agents is the only key to a correct diagnosis, which in turn is essential to avoid improper treatment.</abstract><cop>Pavia</cop><pub>Haematologica</pub><pmid>8647521</pmid><tpages>4</tpages></addata></record> |
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subjects | Adult Age of Onset Biological and medical sciences Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) Danazol - therapeutic use Fanconi Anemia - diagnosis Fanconi Anemia - drug therapy Female Humans Medical genetics Medical sciences |
title | Identification and treatment of late onset Fanconi's anemia |
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