A case of in vivo diagnosis of generalized idiopathic amyloidosis
Author(s) -
D. A. Valimukhametova,
V. N. Leonova,
F. A. Reznikova,
S. K. Khamzina
Publication year - 1988
Publication title -
kazan medical journal
Language(s) - English
Resource type - Journals
eISSN - 2587-9359
pISSN - 0368-4814
DOI - 10.17816/kazmj99764
Subject(s) - amyloidosis , medicine , pathology , disease , amyloid (mycology)
Idiopathic amyloidosis, unlike secondary amyloidosis, develops in the absence of previous disease. Its clinical presentation is multifaceted, determined by the lesion of certain organs and highly variable during the course of the disease. All manifestations of the disease are nonspecific. In contrast to secondary amyloidosis, idiopathic amyloidosis more often involves cardiovascular, respiratory, digestive and urinary systems. In vivo diagnosis of idiopathic amyloidosis is difficult due to its imitation of many diseases; in practice, it is recognized less often than it occurs.
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