Whole-Body MRI Versus Whole-Body MDCT for Staging of Multiple Myeloma
The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess accuracy in staging. Forty-one patients with histologically confirmed myeloma were prospectively examined with a whole-body MDCT protocol and whole...
Saved in:
Published in | American journal of roentgenology (1976) Vol. 190; no. 4; pp. 1097 - 1104 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Leesburg, VA
Am Roentgen Ray Soc
01.04.2008
American Roentgen Ray Society |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess accuracy in staging.
Forty-one patients with histologically confirmed myeloma were prospectively examined with a whole-body MDCT protocol and whole-body MRI on a 1.5-T system. The MRI protocol consisted of T1-weighted spin-echo and STIR sequences. For data analysis, the entire skeleton was divided into 61 regions per patient. Image evaluation was performed in a consensus reading by two radiologists blinded to the patients' history, with separate evaluation of each technique. The patients were staged by MRI and MDCT data separately according to the Durie and Salmon PLUS staging system.
On MRI, 15 patients showed no involvement. In 26 patients, 975 regions were affected: 21 patients were stage I, two were stage II, and 18 were stage III. On MDCT, 19 patients showed no involvement. In 22 patients, 462 regions were affected. For the detection rate, MRI was statistically superior to MDCT (p < 0.001, Wilcoxon's signed rank test). According to MDCT, 25 patients were stage I, seven were stage II, and nine were stage III. In 21 patients with involvement detected on both methods, MRI showed more extensive disease than MDCT. Eleven patients were understaged with MDCT compared with MRI, which was statistically significant (p < 0.001, chi-square test).
Whole-body MDCT leads to a significantly lower detection rate and staging in patients with multiple myeloma. |
---|---|
AbstractList | OBJECTIVE. The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess accuracy in staging. SUBJECTS AND METHODS. Forty-one patients with histologically confirmed myeloma were prospectively examined with a whole-body MDCT protocol and whole-body MRI on a 1.5-T system. The MRI protocol consisted of T1-weighted spin-echo and STIR sequences. For data analysis, the entire skeleton was divided into 61 regions per patient. Image evaluation was performed in a consensus reading by two radiologists blinded to the patients' history, with separate evaluation of each technique. The patients were staged by MRI and MDCT data separately according to the Durie and Salmon PLUS staging system. RESULTS. On MRI, 15 patients showed no involvement. In 26 patients, 975 regions were affected: 21 patients were stage I, two were stage II, and 18 were stage III. On MDCT, 19 patients showed no involvement. In 22 patients, 462 regions were affected. For the detection rate, MRI was statistically superior to MDCT (p < 0.001, Wilcoxon's signed rank test). According to MDCT, 25 patients were stage I, seven were stage II, and nine were stage III. In 21 patients with involvement detected on both methods, MRI showed more extensive disease than MDCT. Eleven patients were understaged with MDCT compared with MRI, which was statistically significant (p < 0.001, chi-square test). CONCLUSION. Whole-body MDCT leads to a significantly lower detection rate and staging in patients with multiple myeloma. The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess accuracy in staging.OBJECTIVEThe purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess accuracy in staging.Forty-one patients with histologically confirmed myeloma were prospectively examined with a whole-body MDCT protocol and whole-body MRI on a 1.5-T system. The MRI protocol consisted of T1-weighted spin-echo and STIR sequences. For data analysis, the entire skeleton was divided into 61 regions per patient. Image evaluation was performed in a consensus reading by two radiologists blinded to the patients' history, with separate evaluation of each technique. The patients were staged by MRI and MDCT data separately according to the Durie and Salmon PLUS staging system.SUBJECTS AND METHODSForty-one patients with histologically confirmed myeloma were prospectively examined with a whole-body MDCT protocol and whole-body MRI on a 1.5-T system. The MRI protocol consisted of T1-weighted spin-echo and STIR sequences. For data analysis, the entire skeleton was divided into 61 regions per patient. Image evaluation was performed in a consensus reading by two radiologists blinded to the patients' history, with separate evaluation of each technique. The patients were staged by MRI and MDCT data separately according to the Durie and Salmon PLUS staging system.On MRI, 15 patients showed no involvement. In 26 patients, 975 regions were affected: 21 patients were stage I, two were stage II, and 18 were stage III. On MDCT, 19 patients showed no involvement. In 22 patients, 462 regions were affected. For the detection rate, MRI was statistically superior to MDCT (p < 0.001, Wilcoxon's signed rank test). According to MDCT, 25 patients were stage I, seven were stage II, and nine were stage III. In 21 patients with involvement detected on both methods, MRI showed more extensive disease than MDCT. Eleven patients were understaged with MDCT compared with MRI, which was statistically significant (p < 0.001, chi-square test).RESULTSOn MRI, 15 patients showed no involvement. In 26 patients, 975 regions were affected: 21 patients were stage I, two were stage II, and 18 were stage III. On MDCT, 19 patients showed no involvement. In 22 patients, 462 regions were affected. For the detection rate, MRI was statistically superior to MDCT (p < 0.001, Wilcoxon's signed rank test). According to MDCT, 25 patients were stage I, seven were stage II, and nine were stage III. In 21 patients with involvement detected on both methods, MRI showed more extensive disease than MDCT. Eleven patients were understaged with MDCT compared with MRI, which was statistically significant (p < 0.001, chi-square test).Whole-body MDCT leads to a significantly lower detection rate and staging in patients with multiple myeloma.CONCLUSIONWhole-body MDCT leads to a significantly lower detection rate and staging in patients with multiple myeloma. The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess accuracy in staging. Forty-one patients with histologically confirmed myeloma were prospectively examined with a whole-body MDCT protocol and whole-body MRI on a 1.5-T system. The MRI protocol consisted of T1-weighted spin-echo and STIR sequences. For data analysis, the entire skeleton was divided into 61 regions per patient. Image evaluation was performed in a consensus reading by two radiologists blinded to the patients' history, with separate evaluation of each technique. The patients were staged by MRI and MDCT data separately according to the Durie and Salmon PLUS staging system. On MRI, 15 patients showed no involvement. In 26 patients, 975 regions were affected: 21 patients were stage I, two were stage II, and 18 were stage III. On MDCT, 19 patients showed no involvement. In 22 patients, 462 regions were affected. For the detection rate, MRI was statistically superior to MDCT (p < 0.001, Wilcoxon's signed rank test). According to MDCT, 25 patients were stage I, seven were stage II, and nine were stage III. In 21 patients with involvement detected on both methods, MRI showed more extensive disease than MDCT. Eleven patients were understaged with MDCT compared with MRI, which was statistically significant (p < 0.001, chi-square test). Whole-body MDCT leads to a significantly lower detection rate and staging in patients with multiple myeloma. |
Author | Baur-Melnyk, Andrea Schoenberg, Stefan Oswald Buhmann, Sonja Reiser, Maximilian Ferdinand Lang, Nicola Bartl, Reiner Becker, Christoph |
Author_xml | – sequence: 1 fullname: Baur-Melnyk, Andrea – sequence: 2 fullname: Buhmann, Sonja – sequence: 3 fullname: Becker, Christoph – sequence: 4 fullname: Schoenberg, Stefan Oswald – sequence: 5 fullname: Lang, Nicola – sequence: 6 fullname: Bartl, Reiner – sequence: 7 fullname: Reiser, Maximilian Ferdinand |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20194194$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/18356461$$D View this record in MEDLINE/PubMed |
BookMark | eNqF0c9rFDEUB_AgLXZbPXmXuagHmfW9JJNkjnWttqWLUOuPW8jMZHYjmcmazLDsf--UXbUIIgQC4fN9hPc9JUd96C0hzxDmlCJ_c359Owc5p4IVj8gMCy5yhhyPyAyYwFwB-3ZCTlP6DgBSlfIxOUHFCsEFzsjF13XwNn8bml22vL3KvtiYxpQ9fH23uMvaELNPg1m5fpWFNluOfnAbb7PlzvrQmSfkuDU-2aeH-4x8fn9xt7jMbz5-uFqc3-Q1UzDkyhYCLMeGG4ZYVJQ2jMq6aoWoKDPIm0YyWhhOmeWVFFaYtgLblKAa2QpkZ-Tlfu4mhh-jTYPuXKqt96a3YUxaKCh5iey_kIJQrFRigs8PcKw62-hNdJ2JO_1rQxN4cQAm1ca30fS1S78dBSz5dCb3eu_qGFKKtv0zCvR9T3rqSYPU9z1NGv_StRvM4EI_ROP8PzKv9pm1W623LlqdOuP99HHU2-0WS9B8CpaS_QTqMJ8N |
CODEN | AAJRDX |
CitedBy_id | crossref_primary_10_1007_s00108_018_0530_2 crossref_primary_10_1016_j_ejrad_2014_02_008 crossref_primary_10_1016_j_ejrad_2013_04_012 crossref_primary_10_1007_s00330_015_3733_0 crossref_primary_10_1556_OH_2014_29881 crossref_primary_10_1038_s41408_018_0124_1 crossref_primary_10_1016_j_diii_2018_12_005 crossref_primary_10_1007_s00234_020_02417_9 crossref_primary_10_1148_radiol_09090629 crossref_primary_10_1016_j_ejrad_2013_08_036 crossref_primary_10_1016_j_rcl_2015_12_008 crossref_primary_10_1007_s00259_017_3730_4 crossref_primary_10_1200_JCO_2010_32_5449 crossref_primary_10_4081_hr_2021_9037 crossref_primary_10_1016_j_ejrad_2015_11_040 crossref_primary_10_1016_j_ncl_2008_09_015 crossref_primary_10_2174_1573405617666210126155129 crossref_primary_10_1155_2011_583439 crossref_primary_10_1016_j_radcr_2020_11_030 crossref_primary_10_1007_s00117_011_2257_0 crossref_primary_10_1016_j_ejrad_2009_03_047 crossref_primary_10_1016_j_ejrad_2009_03_045 crossref_primary_10_3892_mco_2020_2039 crossref_primary_10_1053_j_ro_2024_08_002 crossref_primary_10_1053_j_semnuclmed_2014_08_002 crossref_primary_10_1016_j_cpet_2019_03_004 crossref_primary_10_1007_s00259_024_06858_9 crossref_primary_10_1016_j_jot_2015_07_004 crossref_primary_10_1007_s11654_009_0134_3 crossref_primary_10_1148_radiol_2016142084 crossref_primary_10_2217_ijh_13_61 crossref_primary_10_1007_s00277_009_0829_0 crossref_primary_10_1007_s00330_019_06281_x crossref_primary_10_1067_j_cpradiol_2014_01_003 crossref_primary_10_1097_RCT_0000000000001298 crossref_primary_10_3390_life11121320 crossref_primary_10_1016_j_ejrad_2014_09_012 crossref_primary_10_7314_APJCP_2014_15_22_9879 crossref_primary_10_1016_j_cpet_2018_05_006 crossref_primary_10_1259_bjrcr_20190008 crossref_primary_10_1007_s00256_008_0607_4 crossref_primary_10_1007_s00277_020_04265_2 crossref_primary_10_1007_s00256_023_04277_9 crossref_primary_10_1038_s41598_017_13255_w crossref_primary_10_2214_AJR_17_17984 crossref_primary_10_1016_S0246_0521_11_57251_1 crossref_primary_10_1007_s00330_014_3458_5 crossref_primary_10_1038_bmt_2015_164 crossref_primary_10_1016_j_ejca_2017_03_001 crossref_primary_10_1111_bjh_14545 crossref_primary_10_1259_bjr_20180462 crossref_primary_10_1148_radiol_10091809 crossref_primary_10_1111_bjh_12007 crossref_primary_10_1016_j_ejrad_2016_10_015 crossref_primary_10_1007_s11899_019_00499_8 crossref_primary_10_1016_j_lpm_2024_104263 crossref_primary_10_1016_j_critrevonc_2019_07_002 crossref_primary_10_1016_j_wneu_2023_05_118 crossref_primary_10_1007_s00256_021_03799_4 crossref_primary_10_1007_s00256_024_04723_2 crossref_primary_10_1007_s00330_016_4642_6 crossref_primary_10_1016_j_mric_2018_06_003 crossref_primary_10_1148_radiol_11101746 crossref_primary_10_1016_j_mric_2018_06_005 crossref_primary_10_1038_s41408_020_00360_9 crossref_primary_10_1007_s00117_011_2143_9 crossref_primary_10_1007_s00330_013_2812_3 crossref_primary_10_1016_j_rcl_2008_05_002 crossref_primary_10_1097_MNM_0000000000001470 crossref_primary_10_1007_s00330_010_1950_0 crossref_primary_10_1016_j_mednuc_2017_02_213 crossref_primary_10_1111_ejh_13356 crossref_primary_10_1038_leu_2009_89 crossref_primary_10_1007_s00108_009_2452_5 crossref_primary_10_1007_s11899_016_0314_5 crossref_primary_10_1016_j_mri_2020_08_011 crossref_primary_10_1111_bjh_14827 crossref_primary_10_1007_s00256_018_3066_6 crossref_primary_10_1097_RCT_0000000000001195 crossref_primary_10_1182_blood_2018_08_825356 crossref_primary_10_1016_j_ejrad_2020_109502 crossref_primary_10_2214_AJR_19_21725 crossref_primary_10_1007_s00761_010_1788_8 crossref_primary_10_1007_s00117_009_1971_3 crossref_primary_10_1148_radiol_2522081756 crossref_primary_10_1002_hon_2303 crossref_primary_10_5312_wjo_v5_i3_272 crossref_primary_10_3390_cancers12082113 crossref_primary_10_1186_s13045_017_0549_1 crossref_primary_10_3109_10428194_2012_740559 crossref_primary_10_1007_s00330_013_2792_3 crossref_primary_10_1053_j_sult_2020_08_019 crossref_primary_10_2214_AJR_13_10724 crossref_primary_10_1038_leu_2013_244 crossref_primary_10_1007_s00117_024_01344_7 crossref_primary_10_1093_bjr_tqae183 crossref_primary_10_14412_1996_7012_2024_1_7_14 crossref_primary_10_2214_AJR_21_25878 crossref_primary_10_1002_jmri_26183 crossref_primary_10_2967_jnumed_111_098830 crossref_primary_10_1111_bjh_12346 crossref_primary_10_2214_AJR_16_17219 crossref_primary_10_1111_ejh_12205 crossref_primary_10_1158_1078_0432_CCR_14_1692 crossref_primary_10_12677_ACM_2022_1291270 crossref_primary_10_1007_s40134_018_0298_0 crossref_primary_10_3389_fendo_2018_00436 crossref_primary_10_1200_JCO_2009_25_5356 crossref_primary_10_1007_s00117_013_2628_9 crossref_primary_10_1053_j_sult_2013_05_006 crossref_primary_10_1136_bcr_2015_210896 crossref_primary_10_1016_S1470_2045_09_70088_9 crossref_primary_10_1148_rg_301095066 crossref_primary_10_2217_iim_10_28 crossref_primary_10_1007_s00259_015_3200_9 crossref_primary_10_1016_j_mednuc_2012_02_177 crossref_primary_10_1016_j_crad_2021_05_019 crossref_primary_10_1007_s00256_017_2609_6 crossref_primary_10_1016_j_critrevonc_2011_04_006 crossref_primary_10_1016_j_mri_2020_10_005 crossref_primary_10_1016_j_rcl_2018_09_008 crossref_primary_10_1259_bjr_30649204 crossref_primary_10_2214_AJR_18_20001 crossref_primary_10_3727_036012912X13831831256096 crossref_primary_10_1002_hon_2564 crossref_primary_10_1016_j_urology_2019_04_009 crossref_primary_10_1148_radiol_2017170281 crossref_primary_10_1200_JCO_2014_57_9961 crossref_primary_10_1007_s00330_010_1862_z crossref_primary_10_1016_S1286_935X_12_60820_X crossref_primary_10_1007_s11547_012_0880_0 crossref_primary_10_3238_arztebl_2010_0383 crossref_primary_10_1016_j_ejrad_2009_04_051 crossref_primary_10_3390_cancers12113155 crossref_primary_10_1007_s00330_010_1865_9 crossref_primary_10_1097_CCO_0000000000000230 crossref_primary_10_4143_crt_2014_010 crossref_primary_10_1007_s00256_017_2827_y crossref_primary_10_1007_s00259_013_2520_x crossref_primary_10_1007_s00330_009_1504_5 crossref_primary_10_1007_s00330_017_4907_8 crossref_primary_10_1259_bjr_20180768 crossref_primary_10_1016_j_ejrad_2009_02_005 crossref_primary_10_1007_s12094_010_0565_x crossref_primary_10_1177_02841851211008383 crossref_primary_10_1007_s00117_014_2694_7 crossref_primary_10_1200_JCO_2017_72_2975 crossref_primary_10_1148_radiol_2503081017 crossref_primary_10_1177_2058460117738809 crossref_primary_10_5507_bp_2015_064 crossref_primary_10_1136_bmjopen_2012_002025 crossref_primary_10_4236_ijcm_2012_37115 crossref_primary_10_1007_s00330_009_1443_1 crossref_primary_10_1038_bcj_2017_78 crossref_primary_10_1259_imaging_20110082 crossref_primary_10_17650_1818_8346_2022_17_1_87_94 crossref_primary_10_1016_j_critrevonc_2016_03_006 crossref_primary_10_1038_bcj_2015_57 crossref_primary_10_1016_S0001_4079_19_30259_6 crossref_primary_10_1007_s11547_018_0955_7 crossref_primary_10_1016_j_trsl_2018_05_003 crossref_primary_10_1016_S1879_8551_12_60684_8 crossref_primary_10_1053_j_seminhematol_2010_11_006 crossref_primary_10_1179_1607845414Y_0000000163 crossref_primary_10_1002_ajh_25846 crossref_primary_10_1200_EDBK_159074 crossref_primary_10_1016_j_critrevonc_2018_02_012 |
Cites_doi | 10.1046/j.1365-2141.1997.4213236.x 10.1038/sj.thj.6200312 10.1046/j.1365-2141.1997.1122939.x 10.1148/radiology.201.1.8816551 10.1111/j.1365-2141.1995.tb05363.x 10.4065/80.10.1371 10.1055/s-2001-12920 10.1097/00004424-198803000-00007 10.1016/S0140-6736(87)92383-X 10.2214/ajr.178.6.1781429 10.1046/j.1365-2141.1999.01244.x 10.1200/JCO.1995.13.1.251 10.1046/j.1365-2141.1999.01529.x 10.1148/radiology.154.2.3966137 10.1002/cncr.10818 10.1002/cncr.20697 10.1016/S0308-2261(21)00319-2 10.2214/ajr.167.4.8819407 10.1097/01.rli.0000185878.61270.b0 10.1016/0002-9343(93)90120-E |
ContentType | Journal Article |
Copyright | 2008 INIST-CNRS |
Copyright_xml | – notice: 2008 INIST-CNRS |
DBID | AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM 7T5 H94 7X8 |
DOI | 10.2214/AJR.07.2635 |
DatabaseName | CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Immunology Abstracts AIDS and Cancer Research Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) AIDS and Cancer Research Abstracts Immunology Abstracts MEDLINE - Academic |
DatabaseTitleList | AIDS and Cancer Research Abstracts MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1546-3141 |
EndPage | 1104 |
ExternalDocumentID | 18356461 20194194 10_2214_AJR_07_2635 www190_4_1097 |
Genre | Journal Article |
GroupedDBID | - 1KJ 23M 2WC 34G 39C 53G 55 5GY 5RE AAWTL ABFLS ABOCM ADACO ADBBV AENEX AFFNX AJYGW ALMA_UNASSIGNED_HOLDINGS BAWUL C1A CS3 DIK E3Z EBS EJD F5P GX1 H13 L7B LSO O0- P2P SJN TRR VH1 W2D WH7 WOQ X7M ZA5 --- -DD .55 .GJ 1CY 3O- AAEJM AAYXX AI. AJJEV CITATION J5H MJL TR2 TWZ UDS W8F YJK YQI YQJ ZGI ZVN ZXP IQODW CGR CUY CVF ECM EIF NPM 7T5 H94 7X8 |
ID | FETCH-LOGICAL-c380t-8e560e41d4a3115b22d327cbf66b23a14dd7325a423e4b76e6afb0ed908d7f613 |
ISSN | 0361-803X 1546-3141 |
IngestDate | Thu Jul 10 19:29:57 EDT 2025 Fri Jul 11 07:54:56 EDT 2025 Mon Jul 21 06:05:28 EDT 2025 Mon Jul 21 09:16:41 EDT 2025 Tue Jul 01 00:40:33 EDT 2025 Thu Apr 24 23:03:17 EDT 2025 Tue Nov 10 19:20:18 EST 2020 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 4 |
Keywords | Immunopathology Nuclear medicine Staging Malignant hemopathy Myeloma Nuclear magnetic resonance imaging Multidetector scanner Immunoglobulinopathy Lymphoproliferative syndrome Radiology Medical imagery Whole body Comparative study Cancer |
Language | English |
License | CC BY 4.0 |
LinkModel | OpenURL |
MergedId | FETCHMERGED-LOGICAL-c380t-8e560e41d4a3115b22d327cbf66b23a14dd7325a423e4b76e6afb0ed908d7f613 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PMID | 18356461 |
PQID | 20683986 |
PQPubID | 23462 |
PageCount | 8 |
ParticipantIDs | proquest_miscellaneous_68094913 proquest_miscellaneous_20683986 pubmed_primary_18356461 pascalfrancis_primary_20194194 crossref_primary_10_2214_AJR_07_2635 crossref_citationtrail_10_2214_AJR_07_2635 highwire_smallpub1_www190_4_1097 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2008-04-01 |
PublicationDateYYYYMMDD | 2008-04-01 |
PublicationDate_xml | – month: 04 year: 2008 text: 2008-04-01 day: 01 |
PublicationDecade | 2000 |
PublicationPlace | Leesburg, VA |
PublicationPlace_xml | – name: Leesburg, VA – name: United States |
PublicationTitle | American journal of roentgenology (1976) |
PublicationTitleAlternate | AJR Am J Roentgenol |
PublicationYear | 2008 |
Publisher | Am Roentgen Ray Soc American Roentgen Ray Society |
Publisher_xml | – name: Am Roentgen Ray Soc – name: American Roentgen Ray Society |
References | REF9 REF7 REF8 REF3 REF4 REF11 REF10 REF20 REF15 REF14 REF13 REF12 REF1 atypb1 REF19 REF2 REF18 REF17 atypb2 REF16 |
References_xml | – ident: REF16 doi: 10.1046/j.1365-2141.1997.4213236.x – ident: REF11 doi: 10.1038/sj.thj.6200312 – ident: REF17 doi: 10.1046/j.1365-2141.1997.1122939.x – ident: atypb2 doi: 10.1148/radiology.201.1.8816551 – ident: REF15 doi: 10.1111/j.1365-2141.1995.tb05363.x – ident: REF2 doi: 10.4065/80.10.1371 – ident: REF12 doi: 10.1055/s-2001-12920 – ident: REF8 doi: 10.1097/00004424-198803000-00007 – ident: REF9 doi: 10.1016/S0140-6736(87)92383-X – ident: REF19 doi: 10.2214/ajr.178.6.1781429 – ident: atypb1 doi: 10.1046/j.1365-2141.1999.01244.x – ident: REF7 doi: 10.1200/JCO.1995.13.1.251 – ident: REF10 doi: 10.1046/j.1365-2141.1999.01529.x – ident: REF18 doi: 10.1148/radiology.154.2.3966137 – ident: REF4 doi: 10.1002/cncr.10818 – ident: REF14 doi: 10.1002/cncr.20697 – ident: REF1 doi: 10.1016/S0308-2261(21)00319-2 – ident: REF13 doi: 10.2214/ajr.167.4.8819407 – ident: REF20 doi: 10.1097/01.rli.0000185878.61270.b0 – ident: REF3 doi: 10.1016/0002-9343(93)90120-E |
SSID | ssj0007897 |
Score | 2.3437395 |
Snippet | The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to assess... OBJECTIVE. The purpose of our study was to compare the detection rate of bone manifestations of multiple myeloma in whole-body MRI compared with MDCT and to... |
SourceID | proquest pubmed pascalfrancis crossref highwire |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1097 |
SubjectTerms | Adult Aged Aged, 80 and over Biological and medical sciences Biopsy Female Hematologic and hematopoietic diseases Humans Immunodeficiencies. Immunoglobulinopathies Immunoglobulinopathies Immunopathology Investigative techniques, diagnostic techniques (general aspects) Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis Magnetic Resonance Imaging - methods Male Medical sciences Middle Aged Multiple Myeloma - diagnostic imaging Multiple Myeloma - pathology Neoplasm Staging Salmonidae Statistics, Nonparametric Tomography, X-Ray Computed - methods Whole Body Imaging |
Title | Whole-Body MRI Versus Whole-Body MDCT for Staging of Multiple Myeloma |
URI | http://www.ajronline.org/cgi/content/abstract/190/4/1097 https://www.ncbi.nlm.nih.gov/pubmed/18356461 https://www.proquest.com/docview/20683986 https://www.proquest.com/docview/68094913 |
Volume | 190 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELfKkBAviG_Cx-aHPTEF6sSx3Uc2xsakgLR1om-REztMkCWobVSVP4S_l3NiJ9nUSYOqiirLThPf2Xdn__w7hHZ5ygWJwHOLJJ_4VBLhCypTn6Y5jA-p4WNOI8df2PE5PZlFs9HozwC1VC_Td9nvjedK_keqUAZyNadk_0Gy3U2hAH6DfOEKEobrrWT8zSS39fcrtd6LTz_vmbUvA2gdlH48mDZAQvApv1t8c-wghPFaF5Wdlh0Prdu_GRBKzCuwS4bKtSFrMrxO4FsMFhD2ZT33Y12U658dQrKP8uuLS5uG-awqf_Tl2sE5OnaDfkvoouphZ2dLncPzfF2sZMvs2i1RiAGyxR3NImAKm8S_YHTsTEsZGICW9aqbitvUoVbn6GBiNRvlAyNNbNLi6wYgCAg1RBQnp4aS1RDt9HbO7e1fM38dKBHCIdM8gcbJmCem8R10N4Dww2TGOJr10CEumqQ93Wu15z5N4_eDf77q6Tj2aQO-lQsYf3mbOOXmyKbxcKYP0QMbmuAPrZ49QiNdPkb3Ygu-eIIOe8XCoG64VTc8LAV1w6Bu2KobrnLs1A1bdXuKzj8dTg-OfZuFw89CMV76QoNTrClRVBpmpjQIVBjwLM0ZS4NQEqoUD4NIgl-uacqZZjJPx1pNxkLxHLzFZ2irrEr9AmEuJVMqixTJQkoZuMqK0khzSZXZLRYeeut6LMksRb3JlFIkG2Tjod2u8q-WmWVzNey6PllcyqKALibJarUCXUtoA8Dw0PYVkXS3A-d4QuHroR0nowRmX7OlJktd1QuowSDCEOzmGkyMJ3RCQg89b4XbPywEP4wy8vJ2L_IK3e_H1mu0tZzX-g04xMt0u9HOv2vCsPU |
linkProvider | Geneva Foundation for Medical Education and Research |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Whole-Body+MRI+Versus+Whole-Body+MDCT+for+Staging+of+Multiple+Myeloma&rft.jtitle=American+journal+of+roentgenology+%281976%29&rft.au=Baur-Melnyk%2C+Andrea&rft.au=Buhmann%2C+Sonja&rft.au=Becker%2C+Christoph&rft.au=Schoenberg%2C+Stefan+Oswald&rft.date=2008-04-01&rft.issn=0361-803X&rft.eissn=1546-3141&rft.volume=190&rft.issue=4&rft.spage=1097&rft.epage=1104&rft_id=info:doi/10.2214%2FAJR.07.2635&rft.externalDBID=n%2Fa&rft.externalDocID=10_2214_AJR_07_2635 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0361-803X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0361-803X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0361-803X&client=summon |