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Korean Journal of Urological Oncology ; : 82-87, 2016.
Artículo en Coreano | WPRIM | ID: wpr-23457

RESUMEN

As extra-mammary Paget's disease is rare and usually diagnosed at early stage when it is highly curable with surgical resection, it is much rarer to see patients with recurrent metastatic disease. Thrombotic thrombocytopenic purpura in patients with metastatic solid cancer is also a rare disease and may result from bone marrow metastasis or bone marrow necrosis. For the latter, the majority of cases are not eligible for systemic chemotherapy for rapid disease progression and poor performance status. Herein, authors report a patient with thrombotic thrombocytopenic purpura associated with bone marrow necrosis complicating extra-mammary Paget's disease who was successfully treated with docetaxel and carboplatin combination chemotherapy.


Asunto(s)
Humanos , Médula Ósea , Carboplatino , Progresión de la Enfermedad , Quimioterapia , Quimioterapia Combinada , Necrosis , Metástasis de la Neoplasia , Enfermedad de Paget Extramamaria , Púrpura Trombocitopénica Trombótica , Enfermedades Raras
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