Takayasu’s disease in an IgG4-positive patient with tuberculosis, pulmonary hemorrhage, recurrent myocarditis, and transient bilateral visual impairments


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Abstract

Takayasu’s disease (nonspecific aortoarteritis) affects the absolute majority of 20—40-year-old women; its most common manifestations include aortic arch branch lesions. The specific features of the described case is the male gender of the patient, signs of mesenchymal dysplasia, a concurrence of tuberculosis, pulmonary hemorrhage, and myocarditis at onset, the presence of IgG4, peculiar ocular symptomatology, and its rapid regression after initiation of therapy.

About the authors

O V Blagova

Первый МГМУ им. И.М. Сеченова Минздрава России

Москва, Россия

A V Nedostup

Первый МГМУ им. И.М. Сеченова Минздрава России

Москва, Россия

L V Sherstneva

Научно-исследовательский институт глазных болезней им. Гельмгольца Минздрава России

Москва, Россия

Yu O Grusha

Научно-исследовательский институт глазных болезней им. Гельмгольца Минздрава России

Москва, Россия

S V Gulyaev

Первый МГМУ им. И.М. Сеченова Минздрава России

Москва, Россия

Z S Shapieva

Первый МГМУ им. И.М. Сеченова Минздрава России

Москва, Россия

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