Idiopathic Portal Hypertension in a Patient with Mixed Connective Tissue Disease and Protein C Deficiency

We report a 29-year-old woman with a 2.5 year history of mixed connective tissue disease (MCTD) who developed idiopathic portal hypertension (IPH) and thrombocytopenia as a result of hypersplenism. She had recurrent esophagogastric variceal rupture. Hematological examination also revealed low levels...

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Veröffentlicht in:Internal Medicine 2010, Vol.49(18), pp.2013-2016
Hauptverfasser: Horai, Yoshiro, Miyamura, Tomoya, Hirata, Akie, Nakamura, Masataka, Takahama, Soichiro, Ando, Hitoshi, Minami, Rumi, Yamamoto, Masahiro, Suematsu, Eiichi
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Sprache:eng
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Zusammenfassung:We report a 29-year-old woman with a 2.5 year history of mixed connective tissue disease (MCTD) who developed idiopathic portal hypertension (IPH) and thrombocytopenia as a result of hypersplenism. She had recurrent esophagogastric variceal rupture. Hematological examination also revealed low levels of protein C activity. The liver biopsy specimen showed non-specific mild inflammation and no thrombi. However, portal vein thrombosis developed after splenectomy. This was a rare case of severe complications of IPH accompanying MCTD and protein C deficiency.
ISSN:0918-2918
1349-7235
DOI:10.2169/internalmedicine.49.3834