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1.
Med Princ Pract ; 17(2): 154-6, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18287801

RESUMO

OBJECTIVE: To report a rare case of pleomorphic rhabdomyosarcoma which occurred in the mediastinum of a 34-year-old man. CLINICAL PRESENTATION AND INTERVENTION: A young male labourer presented with dyspnoea on exertion. A large mediastinal mass was detected on chest CT scan. The chest surgeons advised against open biopsy. His alpha-fetoprotein was 22,000 IU/l; based on this the diagnosis of a germ cell tumour was made and the patient was treated with a bleomycin/etoposide/cisplatin regimen. He left for his native country where an open biopsy from the mediastinum was taken and reported as pleomorphic rhabdomyosarcoma. He was given five courses of chemotherapy with doxorubicin, etoposide, and ifosfamide with mesna protection without much relief. The inoperable disease occupied the whole of the right chest and mediastinum. The enormous size of the radiation field made radiotherapy prohibitive. Finally, the patient opted for symptomatic treatment and left for his native place. CONCLUSION: This case is presented because of its difficulty in management and rarity.


Assuntos
Neoplasias do Mediastino , Neoplasias Embrionárias de Células Germinativas , Rabdomiossarcoma , Teratoma , Adulto , Terapia Combinada , Resistencia a Medicamentos Antineoplásicos , Humanos , Masculino , Neoplasias do Mediastino/tratamento farmacológico , Neoplasias do Mediastino/patologia , Neoplasias do Mediastino/cirurgia , Neoplasias Embrionárias de Células Germinativas/tratamento farmacológico , Neoplasias Embrionárias de Células Germinativas/patologia , Neoplasias Embrionárias de Células Germinativas/cirurgia , Rabdomiossarcoma/tratamento farmacológico , Rabdomiossarcoma/patologia , Rabdomiossarcoma/cirurgia , Teratoma/tratamento farmacológico , Teratoma/patologia , Teratoma/cirurgia
2.
Med Princ Pract ; 11(3): 147-9, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12138297

RESUMO

OBJECTIVE: To evaluate the outcome of using radiotherapy (RT) alone to treat patients with early-stage Hodgkin's disease (HD). METHOD: The records of 28 patients with HD treated with RT alone at Kuwait Cancer Control Center between 1980 and 1998 were reviewed. RESULTS: Twenty-three patients had stage I HD and 5 stage II. Two patients had B symptoms, 12 (42.9%) patients lymphocyte-predominant histology, 9 (32.1%) nodular sclerosis and 7 (25%) mixed cellularity. Overall survival and relapse-free survival at 10 years were 100 and 83%, respectively. CONCLUSION: Our data indicate that the use of RT alone for treatment of early stages of HD appears to be effective.


Assuntos
Institutos de Câncer , Doença de Hodgkin/radioterapia , Resultado do Tratamento , Adolescente , Adulto , Intervalo Livre de Doença , Feminino , Pesquisa sobre Serviços de Saúde , Humanos , Kuweit , Masculino , Auditoria Médica , Pessoa de Meia-Idade , Análise de Sobrevida
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