Artaza Varasa T, Alcántara Torres M, Legaz Huidobro M L, Sánchez Ruano J J, López Carriches I, García García J F, Martínez Potenciano J L
Servicio de Gastroenterología, Hospital Virgen de la Salud, Toledo.
Gastroenterol Hepatol. 1996 Dec;19(10):517-8.
The case of a young female diagnosed with an IgG deficit and hepatic granulomas is presented. After 6 years of follow up the patient remains asymptomatic without treatment and with moderate biochemical cholestasis. The tests performed did not lead to a definitive etiologic diagnosis, therefore, according to a review of the literature, we believe that the granulomatous reactions are related with the hypogammaglobulinemia itself.