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Diagnosis and treatment difficulties in 18-year-old male patient with hereditary hemochromatosis, chronic hepatitis B, Gilbert syndrome and ulcerative colitis.
Author(s) -
Katarzyna Sikorska,
Anna Liberek,
Tomasz Romanowski,
Agnieszka SzlagatysSidorkiewicz,
Piotr Landowski,
Krzysztof Piotr Bielawski
Publication year - 2011
Publication title -
acta biochimica polonica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.452
H-Index - 78
eISSN - 1734-154X
pISSN - 0001-527X
DOI - 10.18388/abp.2011_2273
Subject(s) - hereditary hemochromatosis , medicine , ulcerative colitis , hemochromatosis , chronic hepatitis , disease , pediatrics , autoimmune hepatitis , immunology , virus
Among possible causes of chronic hepatitis in adolescents most common are infections, autoimmune disorders and metabolic diseases. Thus, diagnostic procedures should be multidirectional. This study reports diagnosis and treatment difficulties in an 18-year-old male patient with hereditary hemochromatosis (HH), ulcerative colitis (UC), chronic hepatitis B (CHB) and Gilbert syndrome. The presented case illustrates problems in diagnostics related to the presence of numerous disease conditions in one patient. It should be taken into consideration that these diseases coexisting in one patient can mutually affect their symptoms creating specific diagnostic difficulties.

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