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1.
Clin Transplant ; 22(2): 254-7, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18339149

RESUMEN

Generalized lymphedema is an extremely rare effect of sirolimus therapy in renal transplant recipients. We describe the development of this complication in a 56-yr-old woman, who was given an experimental protocol with cyclosporine, sirolimus, steroids, and basiliximab. Following the protocol, after one month, the patient was randomized to the "sirolimus only" group, while cyclosporine was completely suspended and the oral steroids were continued. Three months later, the patient was admitted for severe lymphedema of the lower limbs, with significant weight increase, massive ascites and dyspnea, but excellent renal function. A chest radiography and an ultrasound study of the heart showed a moderate pleural and pericardial effusion. An abdominal ultrasound scan showed two small lymphoceles next to the transplanted kidney, confirmed with a CT scan. After sirolimus discontinuation the generalized lymphedema started to improve and three months later all the symptoms had disappeared.


Asunto(s)
Inmunosupresores/efectos adversos , Trasplante de Riñón/métodos , Linfedema/etiología , Sirolimus/efectos adversos , Femenino , Humanos , Hiperlipidemias/inducido químicamente , Fallo Renal Crónico/cirugía , Trasplante de Riñón/efectos adversos , Persona de Mediana Edad , Ensayos Clínicos Controlados Aleatorios como Asunto
2.
Tumori ; 88(5): 424-6, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12487565

RESUMEN

We report a case of Merkel cell carcinoma (MCC) presenting in the lymph nodes in the absence of a primary cutaneous site. The MCC was treated by palliative radiotherapy, which controlled the disease locally. Eight months after diagnosis a mass appeared on the ipsilateral knee; histopathological examination of this lesion confirmed the diagnosis of MCC. The patient died two months later due to the development of pulmonary metastases. Interestingly, the neoplastic tissue was confined to the regional lymph nodes for several months before the primary site appeared. Primary lymph nodal MCC is rare and the diagnosis is difficult. In our opinion the only way to make a diagnosis of primary lymph nodal MCC is by appropriate clinical follow-up.


Asunto(s)
Carcinoma de Células de Merkel/diagnóstico , Ganglios Linfáticos/patología , Neoplasias Primarias Desconocidas/diagnóstico , Neoplasias Cutáneas/diagnóstico , Anciano , Anciano de 80 o más Años , Carcinoma de Células de Merkel/patología , Diagnóstico Diferencial , Femenino , Ingle , Humanos , Inmunohistoquímica , Metástasis Linfática/diagnóstico , Neoplasias Primarias Desconocidas/patología , Neoplasias Cutáneas/patología , Tomografía Computarizada por Rayos X
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