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1.
Radiology ; 238(3): 1004-12, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16424239

RESUMO

A prospective study approved by the local ethics committee was performed to establish the normal range and reproducibility of myocardial T1 values as assessed with single-breath-hold T1 mapping with high spatial resolution. With a 1.5-T magnetic resonance (MR) imaging system, baseline and contrast material-enhanced modified Look-Locker inversion recovery, or MOLLI, imaging was performed in 15 healthy volunteers who had given written informed consent. Image quality scores and myocardial T1 values were derived for standard short-axis segments and sections. Results were compared with those from a second MR imaging study performed on the same day (baseline only) and those from a third study performed on a different day (baseline and contrast enhanced; eight volunteers). Intra- and interobserver agreement were determined. Myocardial T1 maps were obtained rapidly in a reproducible fashion. A normal range for baseline and postcontrast myocardial T1 was established (baseline mean T1 in short-axis sections, 980 msec +/- 53 [standard deviation]; 95% confidence interval: 964, 997; number of sections, 43). This technique could enable direct quantification of changes in tissue characteristics in ischemic and inflammatory myocardial diseases.


Assuntos
Coração/anatomia & histologia , Imageamento por Ressonância Magnética , Adulto , Meios de Contraste , Feminino , Humanos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Estudos Prospectivos , Valores de Referência , Reprodutibilidade dos Testes
2.
J Hand Surg Am ; 27(1): 154-9, 2002 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11810631

RESUMO

Pleomorphic rhabdomyosarcoma (RMS) is a rare malignancy, and treatment protocols for this tumor are not established. Although Intergroup Rhabdomyosarcoma Study data have led to improvement in overall and disease-free survival for children with juvenile RMS, the applicability of those findings to adult pleomorphic RMS is uncertain. This report presents the case of a 29-year-old man with pleomorphic RMS of the forearm (a location not previously reported in current literature); reviews the immunohistochemical, ultrastructural, and histologic diagnostic criteria; and discusses treatment.


Assuntos
Antebraço/patologia , Rabdomiossarcoma/patologia , Rabdomiossarcoma/ultraestrutura , Neoplasias de Tecidos Moles/patologia , Neoplasias de Tecidos Moles/ultraestrutura , Adulto , Antebraço/cirurgia , Humanos , Masculino , Rabdomiossarcoma/terapia , Neoplasias de Tecidos Moles/terapia
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