Results 81 to 90 of about 12,696 (183)

Síndrome de Ormond: diagnóstico raro en paciente con hipogammaglobulinemia secundaria a rituximab

Revista Alergia México
  Introducción: El síndrome de Ormond, o fibrosis retroperitoneal idiopática, es una enfermedad rara con una incidencia anual de 0.1 a 0.4 casos por cada 100,000 habitantes y una prevalencia de 1.4 por cada 100,000 habitantes.
Jaime Armando Soto Domínguez, Vanessa Daniela Castillo Leon, Alejandra Rodríguez Carbajal, Marya Lizzeth Solis , Noemí Gómez Hernández   +4 more
doaj   +1 more source

Retroperitoneal Fibrosis [PDF]

CJEM, 2015
openaire   +2 more sources

Idiopathic retroperitoneal fibrosis: A case report and review of articles

Basic & Clinical Cancer Research, 2016
Idiopathic retroperitoneal fibrosis is a rare disorder of an unknown etiology characterized by an inflammatory proliferative fibrosing process that may involve the ureters in 80-100% of cases.  The present study was carried on a 38 years old man who was
Sanambar Sadighi, Mohsen Ayati, Mohammad Ali Mohagheghi, Shahriar Shahriaran, Isa Jahanzad, Somaye Safavi   +5 more
doaj  

EL SIGNO DE LA AORTA FLOTANTE THE FLOATING AORTA SIGN

Revista Chilena de Radiología, 2010
El signo de la aorta flotante es causado por voluminosos conglomerados ganglionares que rodean y desplazan hacia anteriora la aorta abdominal, separándola de la columna lumbar, sin evidencias de compresión o estenosis aórtica.
Pablo Cikutovic M, Cristián Varela U, María Carolina Carvajal B   +2 more
doaj  

Retroperitoneal Fibrosis

Journal of Osteopathic Medicine, 2017
Jennifer, Conard, Michelino, Mancini
openaire   +2 more sources

Retroperitoneal Fibrosis [PDF]

Journal of the Royal Society of Medicine, 1979
openaire   +2 more sources

UEG Week 2025 Moderated Posters

United European Gastroenterology Journal, Volume 13, Issue S8, Page S189-S802, October 2025.
wiley   +1 more source

Retroperitoneal Fibrosis [PDF]

Proceedings of the Royal Society of Medicine, 1968
openaire   +2 more sources

Step-by-step robotic technique to manage an extensive retroperitoneal fibrosis. [PDF]

Cent European J Urol, 2023
Di Maida F, Grosso AA, Cadenar A, Gallo ML, Giudici S, Paganelli D, Olivera L, Mari A, Masieri L, Minervini A.   +9 more
europepmc   +1 more source

A Case Report of IgG4-related Disease With Common Clinical Manifestation in an Atypical Gender [PDF]

مجله دانشگاه علوم پزشکی گیلان
Background IgG4-related disease (IgG4-RD) is a recently described clinicopathological condition with a wide range of clinical manifestations including a dense lymphoplasmacytic infiltrate rich in IgG4positive plasma cells, fibrosis arranged in a ...
Seyed Reza Najafizadeh, Maryam Yaseri
doaj