IgG4-LINKED SYSTEMIC DISEASE. MODERN OUTLOOK ON «OLD» DISEASE

Седышев, С. Х.; Vasiliev, V.; Kovriguina, A M; Насонов, Евгений Львович

doi:10.14412/1995-4484-2012-1184

Cited by 6 publications

(2 citation statements)

References 64 publications

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“…IgG4-aссоциированный пахименингит относится к группе IgG4-связанных заболеваний, в которую также вхо-дят аутоиммунный панкреатит 1-го типа, склерозирующий холангит, псевдотумор орбиты и др. [9].…”

Section: нарушение чувствительности 12unclassified

“…Гистологические признаки: а) значительная инфильтрация лимфоцитами и плаз-моцитами с фиброзом без нейтрофильной инфильтрации; b) большое количество IgG4-позитивных клеток в ин-фильтрате (>10 в поле зрения) и/или соотношение IgG4-/ IgG-позитивных клеток > 40%; c) муароформный фиброз; d) облитерирующий флебит. Диагноз устанавливается при наличии следующих критериев: 1+2; 1+3 (a/b); 2+3 (a/b); 3 (a,b,c,d) [5,9,11].…”

Section: нарушение чувствительности 12unclassified

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Hypertrophic pachymeningitis: Current criteria for diagnosis and differentiation (Clinical case and review of literature)

Менделевич

Fattakhova

Богданов

2015

RJTAO

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Section: нарушение чувствительности 12unclassified

Hypertrophic pachymeningitis: Current criteria for diagnosis and differentiation (Clinical case and review of literature)

Менделевич

Fattakhova

Богданов

2015

RJTAO

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Prospects for Anti-B-Cell Therapy in Immuno-Inflammatory Rheumatic Diseases

Насонов

Бекетова²,

Ананьева³

et al. 2019

Naučno-praktičeskaâ revmatologiâ

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Idiopathic multicentric Castleman’s disease

Vasilyev

Palshina

Pavlovskaya

et al. 2020

Terapevticheskii arkhiv

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Idiopathic multicentric Castlemans disease is a rare lymphoproliferative disorder that has many similar laboratory, radiological, clinical and pathological manifestations with various conditions, including IgG4-related disease. Increased activity of cytokines, especially interleukin-6, leads to systemic inflammatory symptoms with the development of lymphadenopathy and rarely extranodal lesions. Histological changes in the lymph nodesin hyaline vascular and plasma cell variants of Castlemans disease are hardly distinguishable from the pattern of reactive, tumor and IgG4-related lymphadenopathy. Idiopathic multicentric Castlemans disease can be diagnosed only when infection with human herpesvirus-8 type and human immunodeficiency virus is excluded. In the article, the authors describe two cases of idiopathic multicentric Castlemans disease, including the first world literature description of extranodal damage of the hip muscle in this disorder. In addition, the authors gave a review of the literature on the main clinical, laboratory and morphological manifestations, which allow confirming the diagnosis of Castlemans disease.

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IgG4-LINKED SYSTEMIC DISEASE. MODERN OUTLOOK ON «OLD» DISEASE

Cited by 6 publications

References 64 publications

Hypertrophic pachymeningitis: Current criteria for diagnosis and differentiation (Clinical case and review of literature)

Hypertrophic pachymeningitis: Current criteria for diagnosis and differentiation (Clinical case and review of literature)

Prospects for Anti-B-Cell Therapy in Immuno-Inflammatory Rheumatic Diseases

Idiopathic multicentric Castleman’s disease

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