LILACS – Literatura Latinoamericana y del Caribe de Ciencias de la Salud

Fibrose hepática congênita e venopatia portal obliterativa sem hipertensão portal - revisão da literatura com base em um caso assintomático

Guerra, Juliana Arrais; Kampa, Kátia Cristina; Zapparoli, Maurício; Alves, Venâncio AF; Ivantes, Cláudia Alexandra Pontes.

Arq. gastroenterol; 55 (4), 2018

ABSTRACT The disease and the case reported here are relevant especially because of their varied clinical presentation, possibility of being associated with other disorders affecting several organs and possible differential diagnoses. Congenital Hepatic Fibrosis is an autosomal recessive disease due to mu...

Enfermedades Asintomáticas, Enfermedades Genéticas Congénitas/complicaciones, Enfermedades Genéticas Congénitas/diagnóstico, Enfermedades Genéticas Congénitas/terapia, Hipertensión Portal/complicaciones, Hipertensión Portal/diagnóstico, Hipertensión Portal/terapia, Hallazgos Incidentales, Cirrosis Hepática/complicaciones, Cirrosis Hepática/congénito, Cirrosis Hepática/diagnóstico, Cirrosis Hepática/terapia, Persona de Mediana Edad, Enfermedades Renales Poliquísticas/complicaciones, Enfermedades Renales Poliquísticas/diagnóstico, Enfermedades Renales Poliquísticas/terapia

Fulltext

Quistes gigantes en la poliquistosis renal. Un indicador poco frecuente de nefrectomía

Zor, Murat; Topuz, Bahad²r; Uguz, Sami; Bedir, Selahattin.

Rev. nefrol. diál. traspl; 38 (3), 2018

A 49-year-old male patient was diagnosed with ADPKD while the evaluation of urinary tract infection in 2010. He was suffering from nutritional problems due to gastro-intestinal disturbances and vomiting secondary to the pressure of the kidneys. He was also a candidate for kidney transplantation, but ther...

Enfermedades Renales Poliquísticas/terapia, Nefrectomía, Quistes/terapia, Trasplante de Riñón

Fulltext