Souhrn doporučení 2013 "Diagnostika a léčba systémové AL amyloidózy"

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Title in English Diagnosis and treatment of systematic AL amyloidosis
Authors

ŠČUDLA Vlastimil ADAM Zdeněk HÁJEK Roman KREJČÍ Marta PIKA Tomáš MAISNAR Vladimír FLODR Patrik KUFOVÁ Zuzana LÁTALOVÁ Pavla POTÁČOVÁ Anna RYŠAVÁ Romana ŠPIČKA Ivan TICHÝ Martin VŠIANSKÁ Pavla

Year of publication 2013
Type Article in Periodical
Magazine / Source Transfuze a hematologie dnes
MU Faculty or unit

Faculty of Medicine

Citation
Field Oncology and hematology
Keywords AL-amyloidosis; diagnosis; treatment; recommendation
Description Amyloidosis is one of the rare disease and in the Czech Republic is diagnosed less often than the actual incidence of the disease. It is a heterogeneous disease affecting with varying severity most of the organs and tissues of the body. Amyloidosis occurs in localized, with only amyloid plaque deposition, but systematic form is much more common, characterized by impairment of many organs and tissues. Due to the infrequent occurrence and low awareness of physicians, amyloidosis escapes early detection, and usually are recognized in advanced stages of the diseases with severe and often irreversible damage of vital organs. Amyloidosis is characterized by a permanent tendency to progression and unfavorable prognosis, since all types of amyloidosis are therapeutically limited to modify. For this reason, we present the following recommendations for diagnosis and treatment.
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