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1.
BMC Cancer ; 20(1): 14, 2020 Jan 06.
Artigo em Inglês | MEDLINE | ID: mdl-31906956

RESUMO

BACKGROUND: Targeted therapies are a standard of care for first-line treatment of Anaplastic lymphoma kinase (ALK)-rearranged non small cell lung cancer (NSCLC). Giving the rapid pace of drug discovery and development in this area, reporting of adverse effects of ALK inhibitors is crucial. Here, we report a case of osteitis induced by an ALK inhibitor mimicking bone metastasis, a previously undescribed side effect of crizotinib. CASE PRESENTATION: A 31-year-old woman with stage IV ALK-rearranged NSCLC presented with back pain after 3 months of crizotinib treatment. Diagnostic work-up showed osteitis on the 4th and 5th thoracic vertebrae, anterior soft tissue infiltration and epiduritis, without any sign of infection. Spinal cord decompression, histological removal and osteosynthesis were performed. Histologic examination showed necrosis with abundant peripheral neutrophils, no microorganism nor malignant cell. Symptoms and Computarized Tomography-abnormalities rapidly diseappeared after crizotinib withdrawal and did not recur after ceritinib onset. CONCLUSIONS: This is the first report of crizotinib-induced osteitis. Crizotinib differs from other ALK inhibitors as it targets other kinases as well, which may have been responsible for the osteitis. Crizotinib can induce rapidly extensive osteitis, which can mimic tumor progression.


Assuntos
Quinase do Linfoma Anaplásico/antagonistas & inibidores , Antineoplásicos/efeitos adversos , Carcinoma Pulmonar de Células não Pequenas/tratamento farmacológico , Crizotinibe/efeitos adversos , Neoplasias Pulmonares/tratamento farmacológico , Osteíte/induzido quimicamente , Inibidores de Proteínas Quinases/efeitos adversos , Adulto , Quinase do Linfoma Anaplásico/genética , Antineoplásicos/uso terapêutico , Neoplasias Ósseas/diagnóstico , Neoplasias Ósseas/secundário , Carcinoma Pulmonar de Células não Pequenas/complicações , Carcinoma Pulmonar de Células não Pequenas/genética , Carcinoma Pulmonar de Células não Pequenas/patologia , Crizotinibe/uso terapêutico , Feminino , Humanos , Neoplasias Pulmonares/complicações , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/patologia , Osteíte/diagnóstico por imagem , Osteíte/patologia , Inibidores de Proteínas Quinases/farmacologia , Pirimidinas/farmacologia , Sulfonas/farmacologia , Tomografia Computadorizada por Raios X
2.
Occup Med (Lond) ; 69(8-9): 632-634, 2019 Dec 31.
Artigo em Inglês | MEDLINE | ID: mdl-31504833

RESUMO

Hypersensitivity pneumonitis (HP) is a chronic inflammatory lung disease caused by repeated inhalation of antigenic substances. We present a case of metalworking fluids (MWFs)-HP sensitized to Pseudomonas oleovorans in a cystic fibrosis patient. This case illustrates that HP diagnosis remains challenging, especially in patients with another pulmonary disease, and that serodiagnosis contributes to identifying the precise microorganism involved. It also demonstrates that P. oleovorans is an important secondary aetiological agent in MWF-HP, less known than Mycobacterium immunogenum.


Assuntos
Alveolite Alérgica Extrínseca/diagnóstico , Fibrose Cística/complicações , Doenças Profissionais/diagnóstico , Adulto , Alveolite Alérgica Extrínseca/tratamento farmacológico , Alveolite Alérgica Extrínseca/etiologia , Alveolite Alérgica Extrínseca/microbiologia , Antígenos de Bactérias , França , Humanos , Óleos Industriais/microbiologia , Masculino , Metalurgia , Doenças Profissionais/imunologia , Doenças Profissionais/microbiologia , Exposição Ocupacional , Pseudomonas oleovorans/imunologia
3.
Can Respir J ; 2016: 4592702, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27445541

RESUMO

Background. Cystic fibrosis-associated liver disease (CFLD) is a major cause of death. The objective of our retrospective study was to describe the relevance of magnetic resonance imaging (MRI) and liver stiffness measurement (LSM) for CFLD evaluation. Methods. All cystic fibrosis adult patients evaluated by MRI and LSM were included. MR signs of portal hypertension (PHT), dysmorphia, or cholangitis were collected and LSM expressed in kPa and Metavir. Results. Of 25 patients, 52% had abnormal MRI. Median LSM was 5.7 kPa (3.4-9.9). Three patients had F2 score and one had F3 score. In patients with PHT, LSM was 7.85 kPa (3.7-9.9) compared to 5 (3.4-7.5) in others, p = 0.02. In patients with abnormal liver function tests, 50% had increased LSM (≥F2), whereas 94% with normal tests had normal LSM (p = 0.04). Seven patients had abnormal MRI despite normal ultrasonography. Conclusions. MRI and LSM provide useful information on CFLD and may help to screen patients with PHT.


Assuntos
Colangiografia , Fibrose Cística/complicações , Técnicas de Imagem por Elasticidade , Imageamento Tridimensional , Hepatopatias/diagnóstico por imagem , Adolescente , Adulto , Feminino , Humanos , Hepatopatias/etiologia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Estudos Retrospectivos , Adulto Jovem
4.
Rev Pneumol Clin ; 72(1): 101-7, 2016 Feb.
Artigo em Francês | MEDLINE | ID: mdl-26209034

RESUMO

Graft-versus-host disease (GVHD) is a classic and frequent multisystemic complication of bone marrow allografts. It has also been reported after the transplantation of solid organs such as the liver or gut. Recent cases of GVHD have been reported after lung and heart-lung transplant. Skin, liver, gastrointestinal tract and bone marrow are the organ preferentially affected by GVHD. Corticosteroid is the first line treatment of GVHD. The prognosis reported in solid organ transplants is poor with infectious complications favoured by immunosuppressive therapy. In this article, we report a case of a patient with cystic fibrosis who presented a probable GVHD 18 months after a lung transplant and a literature review of similar cases.


Assuntos
Fibrose Cística/terapia , Doença Enxerto-Hospedeiro/patologia , Transplante de Pulmão/efeitos adversos , Adulto , Feminino , Humanos , Insuficiência Respiratória/etiologia , Insuficiência Respiratória/terapia
5.
Rev Pneumol Clin ; 72(1): 87-94, 2016 Feb.
Artigo em Francês | MEDLINE | ID: mdl-25727653

RESUMO

Lung transplantation (LT) is now considered as an excellent treatment option for selected patients with end-stage pulmonary diseases, such as COPD, cystic fibrosis, idiopathic pulmonary fibrosis, and pulmonary arterial hypertension. The 2 goals of LT are to provide a survival benefit and to improve quality of life. The 3-step decision process leading to LT is discussed in this review. The first step is the selection of candidates, which requires a careful examination in order to check absolute and relative contraindications. The second step is the timing of listing for LT; it requires the knowledge of disease-specific prognostic factors available in international guidelines, and discussed in this paper. The third step is the choice of procedure: indications of heart-lung, single-lung, and bilateral-lung transplantation are described. In conclusion, this document provides guidelines to help pulmonologists in the referral and selection processes of candidates for transplantation in order to optimize the outcome of LT.


Assuntos
Transplante de Pulmão/métodos , Transplante de Pulmão/estatística & dados numéricos , Seleção de Pacientes , Comportamento de Escolha , Contraindicações , Fibrose Cística/terapia , Humanos , Fibrose Pulmonar Idiopática/terapia , Transplante de Pulmão/normas , Doença Pulmonar Obstrutiva Crônica/terapia , Insuficiência Respiratória/terapia , Fatores de Tempo , Listas de Espera
6.
Arch Pediatr ; 23(12S): 12S33-12S38, 2016 Dec.
Artigo em Francês | MEDLINE | ID: mdl-28231891

RESUMO

This review focused on the news in CF airways infection. International guidelines were provided for the care of non tuberculous mycobacteria, and recent studies stressed on the benefit effect of azithromycin or combined antibiotics. The identification of multiresistant environmental bacteria in airways made to account for little-known consequences. Early diagnosis and eradication of Pseudomonas aeruginosa and Staphylococcus aureus methi-R were still a concern, and reports were proposed. However, the studies on staphylococcus methi-R should be interpreted as regards the European or American continent. Thus, levofloxacine has demonstrated its efficacy without enhancing the efficiency. This drug will increase the choice for treating the patient, but no study were provided on the expected modification of the patient microbiota and the known risk of emergent resistance to antibiotics. Lastly, this review underlined that the CF practitioner was encouraged to search and not underestimate the presence of fungus, of which the not so well studied Aspergillus fumigatus.


Assuntos
Fibrose Cística/diagnóstico , Fibrose Cística/terapia , Infecções Oportunistas/diagnóstico , Infecções Oportunistas/terapia , Infecções Respiratórias/diagnóstico , Infecções Respiratórias/terapia , Criança , Farmacorresistência Bacteriana , Farmacorresistência Bacteriana Múltipla , Diagnóstico Precoce , Intervenção Médica Precoce , Fidelidade a Diretrizes , Humanos , Lactente , Levofloxacino/uso terapêutico , Micoses/diagnóstico , Micoses/terapia , Resultado do Tratamento
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