Clinical case of AL-type amyloidosis
Z.M. NAZIPOVA1, L.R. KHALIULLINA1, А.R. AKHMADEEV2, А.V. КОSTERINA1, M.A. KUNST1
1Kazan State Medical University, 49 Butlerov Str., Kazan, Russian Federation, 420012
2Republic Clinical Hospital of the MH of RT, 138 Orenburgskiy Trakt, Kazan, Russian Federation, 420064
Nazipova Z.M. ― intern of the Department of Hospital Therapy, tel. +7-905-376-21-36, e-mail: zulfira93@mail.ru
Khaliullina L.R. ― intern of the Department of Hospital Therapy, tel. +7-937-288-21-24, e-mail: liana-haliyllina@list.ru
Akhmadeev A.R. ― Head of the Hematology Department, tel. +7-927-240-55-90, e-mail: ahmadeev_ar@mail.ru.
Коsterina A.V. ― Assistant of the Department of Hospital Therapy, tel. +7-917-273-77-68, e-mail: avakost@mail.ru
Kunst M.A. ― Assistant of the Department of Hospital Therapy, tel. +7-904-760-79-20, e-mail: kunstma@mail.ru
The article presents the results of examination of a patient with AL-type amyloidosis. The diagnose was confirmed on the basis of magnetic-resonance tomography of heart, biopsy of rectum with further coloring with Congo red, and immunohistochemical research. The clinical case shows the correct diagnosing in a patient with nonspecific complains.
Key words: amyloid, AL-type amyloidosis, hypertrophic cardiomyopathy, multiple myeloma.
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