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1.
J Vasc Interv Radiol ; 23(6): 786-794.e4, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22626269

RESUMO

PURPOSE: To describe the preliminary safety and accuracy of a magnetic resonance (MR) imaging-guided high-intensity-focused ultrasound (HIFU) system employing new technical developments, including ablation control via volumetric thermal feedback, for the treatment of uterine leiomyomata with histopathologic correlation. MATERIALS AND METHODS: In this phase I clinical trial, 11 women underwent MR-guided HIFU ablation (Sonalleve 1.5T; Philips Medical Systems, Vantaa, Finland), followed by hysterectomy within 30 days. Adverse events, imaging findings, and pathologic confirmation of ablation were assessed. The relationship between MR imaging findings, thermal dose estimates, and pathology and HIFU spatial accuracy were assessed using Bland-Altman analyses and intraclass correlations. RESULTS: There were 12 leiomyomata treated. No serious adverse events were observed. Two subjects decided against having hysterectomy and withdrew from the study before surgery. Of 11 women, 9 underwent hysterectomy; all leiomyomata demonstrated treatment in the expected location. A mean ablation volume of 6.92 cm(3) ± 10.7 was observed at histopathologic examination. No significant differences between MR imaging nonperfused volumes, thermal dose estimates, and histopathology ablation volumes were observed (P > .05). Mean misregistration values perpendicular to the ultrasound beam axis were 0.8 mm ± 1.2 in feet-head direction and 0.1 mm ± 1.0 in and left-right direction and -0.7 mm ± 3.1 along the axis. CONCLUSIONS: Safe, accurate ablation of uterine leiomyomata was achieved with an MR-guided HIFU system with novel treatment monitoring capabilities, including ablation control via volumetric thermal feedback.


Assuntos
Ablação por Ultrassom Focalizado de Alta Intensidade , Leiomioma/cirurgia , Imagem por Ressonância Magnética Intervencionista , Neoplasias Uterinas/cirurgia , Adulto , Feminino , Ablação por Ultrassom Focalizado de Alta Intensidade/efeitos adversos , Humanos , Histerectomia , Leiomioma/patologia , Maryland , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Estudos Prospectivos , Texas , Fatores de Tempo , Resultado do Tratamento , Carga Tumoral , Neoplasias Uterinas/patologia
2.
Obstet Gynecol ; 119(2 Pt 2): 442-444, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22270432

RESUMO

BACKGROUND: In human immunodeficiency virus (HIV)-infected women, Bowen's disease may be difficult to treat successfully with surgery alone. Imiquimod cream, effective in treating Bowen's disease in healthy women, may be a useful postsurgical treatment in immunocompromised women. CASES: Two HIV-infected women had both Bowen's disease and severe cervical dysplasia. In both cases, Bowen's disease, but not cervical dysplasia, recurred after surgical treatment. When treated with topical 5% imiquimod cream twice weekly for 4 months, 70-80% reduction in lesions were observed in both patients. Follow-up biopsies of remaining lesions were vulvar intraepithelial neoplasia 1. CONCLUSION: Imiquimod cream, in combination with surgical treatment, may be an appropriate strategy for treatment of Bowen's disease in HIV-infected and other immunocompromised women.


Assuntos
Aminoquinolinas/uso terapêutico , Antineoplásicos/uso terapêutico , Doença de Bowen/tratamento farmacológico , Neoplasias Cutâneas/tratamento farmacológico , Neoplasias Vulvares/tratamento farmacológico , Adulto , Doença de Bowen/complicações , Doença de Bowen/cirurgia , Feminino , Infecções por HIV/complicações , Infecções por HIV/tratamento farmacológico , Humanos , Imiquimode , Hospedeiro Imunocomprometido , Neoplasias Cutâneas/complicações , Neoplasias Cutâneas/cirurgia , Neoplasias do Colo do Útero/complicações , Neoplasias do Colo do Útero/cirurgia , Neoplasias Vulvares/complicações , Neoplasias Vulvares/cirurgia , Displasia do Colo do Útero/complicações , Displasia do Colo do Útero/cirurgia
3.
Semin Hematol ; 49(1): 83-93, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22221788

RESUMO

Female long-term survivors of allogeneic hematopoietic stem cell transplantation (allo-HSCT) incur a significant burden of late effects. Genital graft-versus-host disease (GVHD), human papillomavirus (HPV) reactivation, ovarian failure and infertility, sexual dysfunction, and osteoporosis are concerns that can significantly impact quality of life. This review examines the risk, pathogenesis, clinical presentation, and implications of these common complications. Recommendations are provided for evaluation and management of these late effects and other obstetric and gynecologic issues that may arise in this patient population.


Assuntos
Doença Enxerto-Hospedeiro/etiologia , Doença Enxerto-Hospedeiro/terapia , Transplante de Células-Tronco Hematopoéticas/efeitos adversos , Infertilidade Feminina/complicações , Osteoporose/complicações , Infecções por Papillomavirus/complicações , Sobreviventes , Feminino , Doença Enxerto-Hospedeiro/complicações , Humanos , Infertilidade Feminina/terapia , Osteoporose/terapia , Infecções por Papillomavirus/terapia , Infecções por Papillomavirus/virologia , Fatores de Tempo , Transplante Homólogo
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