Abstract

Chronic granulomatous disease (CGD) is a primary immunodeficiency (PID), characterized by a defective production of reactive oxygen species by phagocytes. Infectious diseases are a classic manifestation of this form of PID; however, many patients present with a variety of inflammatory and immune non-infectious complications. We analyzed non-infectious complications in a group of 60 patients with CGD, who were treated in Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology (Moscow, Russia) since 2012 to February 2020. This study is supported by the Independent Ethics Committee and approved by the Academic Council of the Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology. Non-infectious manifestations were recorded in 53/60 patients, the most frequent of which were granulomatous complications (81.7% (49/60) of cases) in the following organs - the gastrointestinal tract, lungs, liver and lymph nodes. The median age of granulomas presentation was 3 years, and 45.8% of patients had a combined granulomatous lesion of several organs. Hepatomegaly (40%), splenomegaly (31.7%), dermatitis (21.7%) and chorioretinal lesions (11.3%) were other non-infectious complications. Hematological features outside acute infectious episodes included monocytosis (26.7%), eosinophilia (20%), neutrophilia (13.3%). 96.7% of patients had anemia with a decrease level of serum iron (65%), 31.7% - with signs of hemolysis. Autoimmune manifestations included arthritis, thyroiditis, immune thrombocytopenia or immune neutropenia. Non-infectious complications comprise a significant part of the CGD manifestations and often are the first symptoms of the disease. Awareness of this fact is very important for multidisciplinary approach in treatment of CGD. Delayed diagnosis and immunosuppressive therapy of non-infectious complications without prophylactic antimicrobial therapy can be life-threatening for patients with CGD.

Highlights

  • ФГБУ «Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии им

  • Infectious diseases are a classic manifestation of this form of primary immunodeficiency (PID); many patients present with a variety of inflammatory and immune non-infectious complications

  • We analyzed non-infectious complications in a group of 60 patients with Chronic granulomatous disease (CGD), who were treated in Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology (Moscow, Russia) since 2012 to February 2020

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Summary

ПЕРВИЧНЫЕ ИММУНОДЕФИЦИТЫ И АУТОИММУННЫЕ ЗАБОЛЕВАНИЯ

Инфекционные заболевания являются классическим проявлением данной формы ПИД, тем не менее у многих пациентов наблюдаются различные воспалительные и иммунные неинфекционные осложнения. Нами проведен анализ неинфекционных проявлений у 60 пациентов с диагнозом ХГБ, которые наблюдались в НМИЦ ДГОИ им. У 53/60 пациентов в исследуемой группе зарегистрированы неинфекционные проявления, наиболее частыми из которых были гранулематозные осложнения (81,7% (49/60) случаев) с поражением следующих органов: желудочно-кишечный тракт, легкие, печень и лимфатические узлы. We analyzed non-infectious complications in a group of 60 patients with CGD, who were treated in Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology (Moscow, Russia) since 2012 to February 2020. Аутоиммунные осложнения описаны как при Х-сцепленной, так и при аутосомно-рецессивной формах ХГБ, однако их распространенность и патогенез развития существенно менее изучены. В данной работе мы охарактеризовали неинфекционные «маски» ХГБ, которые крайне разнообразны, затрудняют раннюю постановку истинного диагноза и в связи с этим представляют интерес для широкой медицинской аудитории

МАТЕРИАЛЫ И МЕТОДЫ ИССЛЕДОВАНИЯ
Эритема Erythema Атопия
РЕЗУЛЬТАТЫ ИССЛЕДОВАНИЯ
Immune neutropenia
ОБСУЖДЕНИЕ РЕЗУЛЬТАТОВ ИССЛЕДОВАНИЯ
Findings
Запоры Constipation
Full Text
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