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Severe Ascites in Common Variable Immunodeficiency.
Camões, Guilherme; Fernandes, Diogo A; Ferreira, Diana M; Santos, Arsénio; Carvalho, Armando.
Afiliación
  • Camões G; Internal Medicine, Centro Hospitalar e Universitário de Coimbra, Coimbra, PRT.
  • Fernandes DA; Cardiology, Centro Hospitalar e Universitário de Coimbra, Coimbra, PRT.
  • Ferreira DM; Internal Medicine, Centro Hospitalar e Universitário de Coimbra, Coimbra, PRT.
  • Santos A; Internal Medicine, Centro Hospitalar e Universitário de Coimbra, Coimbra, PRT.
  • Carvalho A; Internal Medicine, Centro Hospitalar e Universitário de Coimbra, Coimbra, PRT.
Cureus ; 14(10): e30274, 2022 Oct.
Article en En | MEDLINE | ID: mdl-36381720
Liver disease is one of the possible clinical manifestations of common variable immunodeficiency and can range from mild hepatomegaly and persistent elevation of liver enzymes to cirrhosis, portal hypertension, and nodular regenerative hyperplasia. The last one is the most common histologic presentation of liver involvement by common variable immunodeficiency and its clinical spectrum can range from asymptomatic to cholestasis, liver cirrhosis, or idiopathic non-cirrhotic portal hypertension, with the severe manifestations being less recognised. We present a case of a 48-year-old woman who was referred for an internal medicine consultation for evaluation of rapidly progressing (span of three months) large-volume ascites and marked asthenia. The patient had a past medical history of common variable immunodeficiency and a recent episode of severe haemolytic anaemia. Peritoneal fluid analyses identified portal hypertension as the cause of the ascites. Abdominal Doppler ultrasound and contrasted abdominal computed tomography confirmed the presence of permeable hepatic and portal veins. Liver biopsy revealed regenerative nodular hyperplasia without cirrhosis. A diagnosis of idiopathic non-cirrhotic portal hypertension secondary to common variable immunodeficiency was made. Treatment was adjusted with considerable improvement in ascites. In conclusion, idiopathic non-cirrhotic portal hypertension is a possible and often overlooked complication in patients with common variable immunodeficiency and is an exclusion diagnosis that requires a high level of suspicion, especially in patients with ascites.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Cureus Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Cureus Año: 2022 Tipo del documento: Article