HEPATOLIENALE GRANULOMATOSE MIT PORTALER HYPERTENSION

Translated title of the contribution: Hepatosplenic granulomatous disease with portal hypertension

E. Windler, G. H. Butzow, G. Kloppel, I. Kempeneers

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

A 40-year-old female patient was admitted with bleeding from esophageal varices. The histology of liver and spleen showed granulomatous infiltrations that had developed without symptoms so far. The portal hypertension and a thrombopenic bleeding diathesis gave rise to the establishment of a splenorenal shunt with extirpation of the spleen. By this the patient could be cured symptomatically, as three years after the acute episode liver functions are still normal. In the light of this case, pathogenesis, the variety of etiologies and the clinical courses of granulomatous liver diseases are discussed in detail with regard to the differential diagnosis.

Translated title of the contributionHepatosplenic granulomatous disease with portal hypertension
Original languageGerman
Pages (from-to)115-122
Number of pages8
JournalZeitschrift fur Gastroenterologie
Volume21
Issue number3
StatePublished - 1983
Externally publishedYes

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