• Лангергансоклеточный гистиоцитоз у ребенка с мультисистемным поражением, инфицированного полиомиелитом и SARS-CoV-2: особенности диагностики и течения болезни. Клинический случай
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Лангергансоклеточный гистиоцитоз у ребенка с мультисистемным поражением, инфицированного полиомиелитом и SARS-CoV-2: особенности диагностики и течения болезни. Клинический случай

Modern Pediatrics. Ukraine. (2023). 1(129): 72-86. doi 10.15574/SP.2023.129.72
Дорош О. И.1,2, Петрончак О. А.3, Масинник Ю. С.4, Гулей Р. В.3, Дудаш А. П.3, Фэш Н. А.3Тимчишин С. М.1, Литвин Г. О.2
1 КНП Львовского областного совета «Западноукраинский специализированный детский медицинский центр», Украина
2 Львовский национальный медицинский университет имени Данилы Галицкого, Украина
3 ООО «Западноукраинская гистологическая лаборатория», г. Львов, Украина
4 Центр медицинских инноваций «NOVO», г. Львов, Украина

Для цитирования: Dorosh OI, Petronchak OA, Masynnyk YuS, Guley RV et al. (2023). Langerhans cell histiocytosis in a child with multisystemic lesions associated with infected poliomyelitis and SARS-CoV-2, features of diagnostics. Clinical case. Modern Pediatrics. Ukraine. 1(129): 72-86. doi 10.15574/SP.2023.129.72.
Статья поступила в редакцию 30.11.2022 г., принята в печать 07.02.2023 г.

Лангергансоклеточный гистиоцитоз (ЛКГ) — редкое заболевание, морфологической основой которого является клональная пролиферация патологических клеток Лангерганса. Клинические проявления ЛКГ колеблются от локализованных форм с доброкачественным течением и спонтанным выздоровлением до мультисистемного поражения с тяжелым течением и летальным исходом. В патологический процесс могут вовлекаться любые органы и системы в разном сочетании (моно- и мультисистемное поражение). Для пациентов с мультисистемной формой ЛКГ и привлечением органов риска (печени, селезенки, костного мозга) характерны отрицательный ответ на стандартную терапию и неблагоприятный прогноз. Поражение кожи является классическим признаком ЛКГ.
Цель — описать сложность и продолжительность диагностики ЛКГ с мультисистемным поражением у мальчика в возрасте 2 года 2 месяца, инфицированного полиомиелитом и коронавирусом.
Клинический случай. Первые клинические проявления ЛКГ у ребенка дебютировали экзематозно-себорейной сыпью волосистой части головы с распространением на конечности, туловище. Ребёнка лечили по месту жительства от токсикодермии, геморрагического васкулита в течение 6 мес. Мальчик потерял 1,5 кг в массе тела за 1 мес. На момент госпитализации наблюдались себорейно-экзематозные высыпания на коже с геморрагическим компонентом, трофически-воспалительные изменения ногтей рук, признаки белково-энергетической недостаточности, стоматит, гингивит, гепатоспленомегалия, полисерозит, несахарный диабет. По результатам анализов: анемия, тромбоцитопения, гипопротеин- и гипоальбуминемия, коагулогические расстройства. У пациента наблюдалось появление нижнего вялого парапареза, мышечная гипотония, ребенок перестал удерживать голову, не мог сидеть. У мальчика диагностирован ряд инфекционных осложнений, в т.ч. полиомиелит (дериват вакцинного полиовируса типа 2 (VDPV2)), коронавирусная болезнь 19 (COVID-19). Ребенок получил цитостатическую терапию LCH III с положительным эффектом.
Ввиду низкого охвата детского населения в Украине прививками при наличии параличей или парезов у детей следует обязательно проводить лабораторное обследование на наличие полиовирусов в фекалиях. Медицинскому сообществу следует пропагандировать необходимость проведения обязательных профилактических прививок детям.
Исследование выполнено в соответствии с принципами Хельсинкской декларации. На проведение исследований получено информированное согласие пациента.
Авторы заявляют об отсутствии конфликта интересов.
Ключевые слова: лангергансоклеточный гистиоцитоз, полиомиелит, коронавирусная инфекция (SARS-CoV-2/СOVID-19), цитостатическая терапия, дети.
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