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thrombocythemia
anoreksi parestesi
最終更新： 2008-03-04
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diagnostic guidelines for essential thrombocythemia should be followed carefully and diagnosis reassessed periodically in cases of uncertainty, with effort made to distinguish from hereditary or secondary thrombocytosis, which may include genetic analysis and bone marrow biopsy.
diagnostiske retningslinjer for essentiel trombocytæmi bør følges nøje, og ved usikkerhed bør diagnosen revurderes regelmæssigt med bestræbelser på at differentiere mellem hereditær og sekundær trombocytose, hvilket kan omfatte genetisk analyse og knoglemarvsbiopsi.
leucopenia lymphoma like reaction, lymphadenopathy, hypochromic anaemia1,2,3, blood dyscrasia, purpura, coagulation disorder, coagulation time increased2,3, anaemia1, thrombocytopenia3, thrombocythemia, eosinophilia1, leukocytosis2, lymphocytosis
leukopeni lymfom- lignende reaktion, lymfadenopati, hypokrom anæmi1, 2, 3 bloddyskrasi, purpura, koagulationsforstyrrelse, øget koagulationstid2, 3, anæmi1, trombocytopeni3, trombocytæmi, eosinofili1, leukocytose2, lymfocytose