Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
1.
Arch Dis Child Educ Pract Ed ; 105(2): 66-70, 2020 04.
Artigo em Inglês | MEDLINE | ID: mdl-31278078

RESUMO

Leukaemia is the most common cancer of childhood. Most children with a new diagnosis of leukaemia are clinically stable at initial presentation. However, there are a number of life-threatening complications that have to be considered and monitored for. These complications include sepsis, tumour lysis syndrome, mediastinal masses, bleeding and pain. The aim of this article is to equip the general paediatrician with a framework for managing children with suspected leukaemia, prior to transfer to the primary treatment centre. The presentation, diagnosis and definitive treatment of acute leukaemia is not in the remit of this article.


Assuntos
Leucemia Mieloide Aguda/diagnóstico , Pediatria , Leucemia-Linfoma Linfoblástico de Células Precursoras/diagnóstico , Encaminhamento e Consulta , Criança , Diagnóstico Diferencial , Humanos , Leucemia Mieloide Aguda/complicações , Leucemia Mieloide Aguda/terapia , Leucemia-Linfoma Linfoblástico de Células Precursoras/complicações , Leucemia-Linfoma Linfoblástico de Células Precursoras/terapia , Síndrome de Lise Tumoral/complicações , Síndrome de Lise Tumoral/diagnóstico
3.
J Neuroophthalmol ; 35(2): 168-70, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25742058

RESUMO

Plasmacytoma of the orbit secondary to multiple myeloma is rare and has not previously been reported limited to an extraocular muscle. Conventional treatment is either localized radiotherapy or systemic chemotherapy. We report a case of plasmacytoma within the medial rectus muscle, which regressed completely with localized infiltration of dexamethasone.


Assuntos
Antineoplásicos Hormonais/uso terapêutico , Dexametasona/uso terapêutico , Músculos Oculomotores/efeitos dos fármacos , Músculos Oculomotores/fisiopatologia , Plasmocitoma/tratamento farmacológico , Idoso , Anticorpos Monoclonais/metabolismo , Antígenos CD/metabolismo , Humanos , Imageamento por Ressonância Magnética , Masculino , Melanócitos/metabolismo , Melanócitos/patologia , Tomografia Computadorizada por Raios X
5.
Blood Adv ; 8(17): 4563-4567, 2024 Sep 10.
Artigo em Inglês | MEDLINE | ID: mdl-38968147

RESUMO

ABSTRACT: Pediatric thrombotic thrombocytopenic purpura (TTP) is an ultrarare disease. Immune TTP (iTTP) is driven by anti-ADAMTS13 autoantibodies causing an imbalanced von Willebrand factor (VWF):ADAMTS13 axis, and rarer still in children, but potentially life-threatening. Caplacizumab is licensed for iTTP treatment in adults and adolescents aged ≥12 years who weigh ≥40 kg. There is a need to clarify whether caplacizumab can be used in younger children. We retrospectively described caplacizumab use in 16 patients under 18 years of age from the UK TTP Registry, including 4 children aged <12 years. For patients weighing <40 kg (n = 3), caplacizumab was dosed at 5 mg once dailyThe youngest patient was 33 months old at diagnosis. Plasma exchange (PEX) was used in 15 patients, with a median of 5 exchanges required before platelet count normalization (range, 2-9). One patient was managed without PEX. All patients achieved normalization of platelet count (median, 5.5 days; range, 3-28) and ADAMTS13 activity (median, 35 days; range, 8-149), with a median hospital admission of 11 days (range, 5-26). There were no refractory patients. One patient relapsed 9 months after presentation. Bleeding requiring VWF supplementation and reduction of caplacizumab use occurred in 1 patient with severe epistaxis, with no significant intracranial or gastrointestinal bleeding. We demonstrated the efficacy and safety of caplacizumab in the pediatric population, which is synonymous with the adult trial data: primarily, reduction of PEX compared with the precaplacizumab era. This has implications for the intensification and duration of admission, particularly relevant in pediatric care.


Assuntos
Púrpura Trombocitopênica Trombótica , Sistema de Registros , Anticorpos de Domínio Único , Humanos , Púrpura Trombocitopênica Trombótica/tratamento farmacológico , Púrpura Trombocitopênica Trombótica/terapia , Criança , Anticorpos de Domínio Único/uso terapêutico , Reino Unido , Pré-Escolar , Feminino , Masculino , Adolescente , Lactente , Proteína ADAMTS13 , Estudos Retrospectivos , Resultado do Tratamento , Contagem de Plaquetas , Troca Plasmática
6.
PLoS One ; 10(9): e0136207, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26367874

RESUMO

Double relapsed and/or refractory multiple myeloma (DRMM), MM that is relapsed and/or refractory to bortezomib and lenalidomide, carries a poor prognosis. The healthcare costs of DRMM have not previously been reported. We analyzed detailed medical resource utilization (MRU) costs, drug costs and outcomes for 39 UK patients receiving standard DRMM therapy. Median OS in this cohort was 5.6 months. The mean cost of DRMM treatment plus MRU until death was £23,472 [range: £1,411-£90,262], split between drug costs £11,191 and other resource use costs £12,281. The cost per assumed quality-adjusted life year (QALY) during DRMM was £66,983. These data provide a standard of care comparison when evaluating the cost-effectiveness of new drugs in DRMM.


Assuntos
Antineoplásicos/economia , Bortezomib/economia , Análise Custo-Benefício , Mieloma Múltiplo/economia , Talidomida/análogos & derivados , Idoso , Antineoplásicos/uso terapêutico , Bortezomib/uso terapêutico , Feminino , Humanos , Lenalidomida , Masculino , Pessoa de Meia-Idade , Mieloma Múltiplo/tratamento farmacológico , Mieloma Múltiplo/epidemiologia , Recidiva , Talidomida/economia , Talidomida/uso terapêutico , Reino Unido
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA