Allogeneic Bone Marrow Transplantation in a Patient with Chemotherapy-Resistant Progressive Histiocytosis X
HISTIOCYTOSIS X is the name for a spectrum of rare disorders — Letterer–Siwe disease, Hand–Schüller–Christian disease, and eosinophilic granuloma 1 2 3 — that have a wide range of clinical manifestations but are all characterized by granuloma formation, with infiltration and proliferation of histioc...
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| Veröffentlicht in: | The New England journal of medicine 1987-03, Vol.316 (12), p.733-735 |
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| container_title | The New England journal of medicine |
| container_volume | 316 |
| creator | Ringdén, Olle Åhström, Lars Lönnqvist, Berit Båryd, Ingvar Svedmyr, Erik Gahrton, Gösta |
| description | HISTIOCYTOSIS X is the name for a spectrum of rare disorders — Letterer–Siwe disease, Hand–Schüller–Christian disease, and eosinophilic granuloma
1
2
3
— that have a wide range of clinical manifestations but are all characterized by granuloma formation, with infiltration and proliferation of histiocytes.
In many cases, the symptoms include pain caused by one or more bone lesions. Lymph-node involvement occurs frequently in younger patients. The benign forms of histiocytosis X are characterized by spontaneous remissions and exacerbations. Disseminated fulminant disease progresses rapidly and has an unfavorable outcome. The diagnosis is based on histologie criteria, which can be used as guidelines for prognosis . . . |
| doi_str_mv | 10.1056/NEJM198703193161207 |
| format | Article |
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1
2
3
— that have a wide range of clinical manifestations but are all characterized by granuloma formation, with infiltration and proliferation of histiocytes.
In many cases, the symptoms include pain caused by one or more bone lesions. Lymph-node involvement occurs frequently in younger patients. The benign forms of histiocytosis X are characterized by spontaneous remissions and exacerbations. Disseminated fulminant disease progresses rapidly and has an unfavorable outcome. The diagnosis is based on histologie criteria, which can be used as guidelines for prognosis . . .</description><identifier>ISSN: 0028-4793</identifier><identifier>EISSN: 1533-4406</identifier><identifier>DOI: 10.1056/NEJM198703193161207</identifier><identifier>PMID: 3547128</identifier><identifier>CODEN: NEJMAG</identifier><language>eng</language><publisher>Boston, MA: Massachusetts Medical Society</publisher><subject>Adult ; Biological and medical sciences ; Bone Marrow Transplantation ; DNA - biosynthesis ; Drug Resistance ; Eosinophilic Granuloma - therapy ; Graft vs Host Disease - prevention & control ; Hematologic and hematopoietic diseases ; Histiocytosis, Langerhans-Cell - therapy ; Humans ; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis ; Lymphocytes - metabolism ; Male ; Medical sciences ; Transplantation, Homologous</subject><ispartof>The New England journal of medicine, 1987-03, Vol.316 (12), p.733-735</ispartof><rights>1987 INIST-CNRS</rights><rights>Copyright Massachusetts Medical Society Mar 19, 1987</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c393t-d653c0a29bb2df5e416bd44bcf60d68e4da1f4fc143b12bc1df1e3b5688e1f173</citedby><cites>FETCH-LOGICAL-c393t-d653c0a29bb2df5e416bd44bcf60d68e4da1f4fc143b12bc1df1e3b5688e1f173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.proquest.com/docview/1884194243?pq-origsite=primo$$EHTML$$P50$$Gproquest$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,64385,64387,64389,72469</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8272308$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3547128$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ringdén, Olle</creatorcontrib><creatorcontrib>Åhström, Lars</creatorcontrib><creatorcontrib>Lönnqvist, Berit</creatorcontrib><creatorcontrib>Båryd, Ingvar</creatorcontrib><creatorcontrib>Svedmyr, Erik</creatorcontrib><creatorcontrib>Gahrton, Gösta</creatorcontrib><title>Allogeneic Bone Marrow Transplantation in a Patient with Chemotherapy-Resistant Progressive Histiocytosis X</title><title>The New England journal of medicine</title><addtitle>N Engl J Med</addtitle><description>HISTIOCYTOSIS X is the name for a spectrum of rare disorders — Letterer–Siwe disease, Hand–Schüller–Christian disease, and eosinophilic granuloma
1
2
3
— that have a wide range of clinical manifestations but are all characterized by granuloma formation, with infiltration and proliferation of histiocytes.
In many cases, the symptoms include pain caused by one or more bone lesions. Lymph-node involvement occurs frequently in younger patients. The benign forms of histiocytosis X are characterized by spontaneous remissions and exacerbations. Disseminated fulminant disease progresses rapidly and has an unfavorable outcome. The diagnosis is based on histologie criteria, which can be used as guidelines for prognosis . . .</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation</subject><subject>DNA - biosynthesis</subject><subject>Drug Resistance</subject><subject>Eosinophilic Granuloma - therapy</subject><subject>Graft vs Host Disease - prevention & control</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Histiocytosis, Langerhans-Cell - therapy</subject><subject>Humans</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Lymphocytes - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Transplantation, Homologous</subject><issn>0028-4793</issn><issn>1533-4406</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kVFrFDEQx4Mo9Vr9BCIEFF9kNZNkN9nHelSrtFqkgm9LNjvby7mbnEmu5b69KXf0QcR5yZD_b_6TzBDyAtg7YHXz_uvZl0totWICWgENcKYekQXUQlRSsuYxWTDGdSVVK56S45TWrATI9ogciVoq4HpBfp1OU7hBj87SD8EjvTQxhjt6HY1Pm8n4bLILnjpPDb0qOfpM71xe0eUK55BXGM1mV33H5FIuNL2K4SZiSu4W6Xm5c8Hucigq_fmMPBnNlPD54TwhPz6eXS_Pq4tvnz4vTy8qK1qRq6GphWWGt33Ph7FGCU0_SNnbsWFDo1EOBkY5WpCiB95bGEZA0deN1ggjKHFC3ux9NzH83mLK3eySxan8BsM2dUpJqFXLCvjqL3AdttGXt3WgtYRWcikKJfaUjSGliGO3iW42cdcB6-4X0f1jEaXq5cF72884PNQcJl_01wfdJGumsczbuvSAaa64YPfY2z02z6nzuJ7_2_QPs6Cdsg</recordid><startdate>19870319</startdate><enddate>19870319</enddate><creator>Ringdén, Olle</creator><creator>Åhström, Lars</creator><creator>Lönnqvist, Berit</creator><creator>Båryd, Ingvar</creator><creator>Svedmyr, Erik</creator><creator>Gahrton, Gösta</creator><general>Massachusetts Medical Society</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>0TZ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K0Y</scope><scope>LK8</scope><scope>M0R</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>19870319</creationdate><title>Allogeneic Bone Marrow Transplantation in a Patient with Chemotherapy-Resistant Progressive Histiocytosis X</title><author>Ringdén, Olle ; Åhström, Lars ; Lönnqvist, Berit ; Båryd, Ingvar ; Svedmyr, Erik ; Gahrton, Gösta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-d653c0a29bb2df5e416bd44bcf60d68e4da1f4fc143b12bc1df1e3b5688e1f173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation</topic><topic>DNA - biosynthesis</topic><topic>Drug Resistance</topic><topic>Eosinophilic Granuloma - therapy</topic><topic>Graft vs Host Disease - prevention & control</topic><topic>Hematologic and hematopoietic diseases</topic><topic>Histiocytosis, Langerhans-Cell - therapy</topic><topic>Humans</topic><topic>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Lymphocytes - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Transplantation, Homologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ringdén, Olle</creatorcontrib><creatorcontrib>Åhström, Lars</creatorcontrib><creatorcontrib>Lönnqvist, Berit</creatorcontrib><creatorcontrib>Båryd, Ingvar</creatorcontrib><creatorcontrib>Svedmyr, Erik</creatorcontrib><creatorcontrib>Gahrton, Gösta</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>Pharma and Biotech Premium PRO</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>New England Journal of Medicine</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>Psychology Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>The New England journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ringdén, Olle</au><au>Åhström, Lars</au><au>Lönnqvist, Berit</au><au>Båryd, Ingvar</au><au>Svedmyr, Erik</au><au>Gahrton, Gösta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Allogeneic Bone Marrow Transplantation in a Patient with Chemotherapy-Resistant Progressive Histiocytosis X</atitle><jtitle>The New England journal of medicine</jtitle><addtitle>N Engl J Med</addtitle><date>1987-03-19</date><risdate>1987</risdate><volume>316</volume><issue>12</issue><spage>733</spage><epage>735</epage><pages>733-735</pages><issn>0028-4793</issn><eissn>1533-4406</eissn><coden>NEJMAG</coden><abstract>HISTIOCYTOSIS X is the name for a spectrum of rare disorders — Letterer–Siwe disease, Hand–Schüller–Christian disease, and eosinophilic granuloma
1
2
3
— that have a wide range of clinical manifestations but are all characterized by granuloma formation, with infiltration and proliferation of histiocytes.
In many cases, the symptoms include pain caused by one or more bone lesions. Lymph-node involvement occurs frequently in younger patients. The benign forms of histiocytosis X are characterized by spontaneous remissions and exacerbations. Disseminated fulminant disease progresses rapidly and has an unfavorable outcome. The diagnosis is based on histologie criteria, which can be used as guidelines for prognosis . . .</abstract><cop>Boston, MA</cop><pub>Massachusetts Medical Society</pub><pmid>3547128</pmid><doi>10.1056/NEJM198703193161207</doi><tpages>3</tpages></addata></record> |
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| ispartof | The New England journal of medicine, 1987-03, Vol.316 (12), p.733-735 |
| issn | 0028-4793 1533-4406 |
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| subjects | Adult Biological and medical sciences Bone Marrow Transplantation DNA - biosynthesis Drug Resistance Eosinophilic Granuloma - therapy Graft vs Host Disease - prevention & control Hematologic and hematopoietic diseases Histiocytosis, Langerhans-Cell - therapy Humans Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Lymphocytes - metabolism Male Medical sciences Transplantation, Homologous |
| title | Allogeneic Bone Marrow Transplantation in a Patient with Chemotherapy-Resistant Progressive Histiocytosis X |
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