Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Int J Surg Pathol ; 31(1): 76-81, 2023 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-35593119

RESUMO

Synovial sarcomas are high-grade soft tissue sarcomas of primitive mesenchymal origin which are defined by a pathognomonic t(X;18)(p11,q11) translocation, and which occur in pediatric and adult populations. Herein we report a case of a 33-year-old female with a history of nasopharyngeal carcinoma status post radiotherapy, presenting with a poorly differentiated synovial sarcoma of the nasal cavity arising in the radiation field. While the development of radiation-associated sarcoma is a known complication of radiotherapy, to date only 10 cases of synovial sarcoma have been reported to occur in previously irradiated tissues. Moreover, only 1 case of poorly differentiated synovial sarcoma involving the nasopharynx has been described.


Assuntos
Sarcoma Sinovial , Neoplasias de Tecidos Moles , Adulto , Feminino , Humanos , Criança , Sarcoma Sinovial/diagnóstico , Sarcoma Sinovial/patologia , Cavidade Nasal/patologia , Proteínas de Fusão Oncogênica
2.
Case Rep Hematol ; 2018: 9071693, 2018.
Artigo em Inglês | MEDLINE | ID: mdl-30271643

RESUMO

Acute myeloid leukemia (AML) can present with extramedullary involvement known as myeloid sarcoma (MS). We present the case of a young woman who was diagnosed with AML and MS in bilateral orbits, brain, omentum, and retroperitoneum. She was treated with induction chemotherapy. Low-dose radiation was given to the orbits due to visual symptoms which resulted in complete response. The use of radiation therapy in orbital MS has not been studied extensively, and low dose may be adequate to achieve complete remission (CR) in selected patients.

3.
Case Rep Hematol ; 2014: 359158, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24822133

RESUMO

Little information is available regarding late relapse in patients with T-lymphoblastic leukemia/lymphoma (T-LBL). Because of the aggressive nature of this disease, relapse is common and often happens early. Late relapses are rare and generally occur within a few years after initial remission. The relapse rate after 3 years has been reported to steadily decrease over time yet does not parallel with cure. We report a case of a 26-year-old female with T-LBL and relapse 16 years after her first remission with successful treatment with HyperCVAD and L-asparaginase.

SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA