A CLINICAL CASE OF MUCOSIS FUNGOIDES
Abstract
Mucosis fungoides (Sezary syndrome) is a rare disease. Because of polymorphism of clinical manifestations that mimic benign diseases of the skin, it often takes several years before the disease is diagnosed. The paper presents a clinical case of progressive mucosis fungoides with unfavorable outcome. The diagnosis of mycosis fungoides was first suspected on the basis of laboratory studies of peripheral blood.
About the Authors
Е. S. Filimonova
Clinical Hospital № 42, Zelenogorsk, Krasnoyarsk Krai
Russian Federation
Russian Federation
Yu. А. Dykhno
V.F. Voino-Yasenetsky Krasnoyarsk State Medical University, Krasnoyarsk
Russian Federation
Russian Federation
S. L. Tarasenko
Clinical Hospital № 42, Zelenogorsk, Krasnoyarsk Krai
Russian Federation
Russian Federation
Е. V. Asadulina
Clinical Hospital № 42, Zelenogorsk, Krasnoyarsk Krai
Russian Federation
Russian Federation
T. L. Kravchuk
Tomsk Cancer Research Institute
Russian Federation
23-g, Komsomolskaya Street, 663690-Zelenogorsk, Krasnoyarsk Krai
Russian Federation
23-g, Komsomolskaya Street, 663690-Zelenogorsk, Krasnoyarsk Krai
D. M. Podoplekin
Tomsk Cancer Research Institute
Russian Federation
23-g, Komsomolskaya Street, 663690-Zelenogorsk, Krasnoyarsk Krai
Russian Federation
23-g, Komsomolskaya Street, 663690-Zelenogorsk, Krasnoyarsk Krai
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Review
For citations:
Filimonova Е.S., Dykhno Yu.А., Tarasenko S.L., Asadulina Е.V., Kravchuk T.L., Podoplekin D.M. A CLINICAL CASE OF MUCOSIS FUNGOIDES. Siberian journal of oncology. 2014;(6):64-68. (In Russ.)
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