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"code": "D70",
"name": "Агранулоцитоз",
"icd_name": "Агранулоцитоз",
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"cause": [
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"periodicity": 1,
"slug": "d70_agranulocitoz",
"lead": "Нарушение здоровья, относящееся к группе другие болезни крови и кроветворных органов",
"description": " \r\nАгранулоцитоз – клинико-лабораторный синдром, основное проявление которого состоит в резком снижении или полном отсутствии нейтрофильных гранулоцитов в периферической крови, что сопровождается повышением восприимчивости организма к грибковым и бактериальным инфекциям. \r\n",
"etiology": "<p>К причинам развития агранулоцитоза относят: </p>\r\n<ul>\r\n<li>Ионизирующая радиация и лучевая терапия, химические вещества (бензол), инсектициды. </li>\r\n<li>Лекарственные средства могут вызвать агранулоцитоз в результате прямого угнетения кроветворения (цитостатики, вальпроевая кислота, карбамазепин, бета-лактамные антибиотики), либо действуя как гаптены (препараты золота, антитиреоидные препараты и пр.). </li>\r\n<li>Аутоиммунные заболевания (например, красная волчанка, аутоиммунный тиреоидит). </li>\r\n<li>Вирусные инфекции (вызванные вирусом Эпштейна – Барра, цитомегаловирус, желтая лихорадка, вирусные гепатиты) обычно сопровождаются умеренной нейтропенией, однако в некоторых случаях может развиться агранулоцитоз. </li>\r\n<li>Тяжелые генерализованные инфекции (как бактериальные, так и вирусные). </li>\r\n<li>Исхудание. </li>\r\n<li>Генетические нарушения. </li>\r\n</ul>",
"pathogenesis": "<p>В зависимости от причины возникновения и механизма развития патологии, различают следующие виды агранулоцитоза: </p>\r\n<ol>\r\n<li>Миелотоксический.</li>\r\n<li>Иммунный: аутоиммунный;гаптеновый. </li>\r\n<li>Генуинный.</li>\r\n</ol>\r\n<p>Миелотоксический агранулоцитоз возникает в результате подавляющего воздействия неблагоприятных факторов на красный костный мозг, и представляет собой глубокую депрессию кроветворного ростка, ответственного за продукцию гранулоцитов. </p>\r\n<p>В основе аутоиммунного агранулоцитоза лежит патологическая реакция иммунной системы, сопровождающаяся образованием антител к собственным нейтрофилам. Такая разновидность агранулоцитоза встречается при аутоиммунном тиреоидите, ревматоидном артрите, системной красной волчанке и других коллагенозах. Агранулоцитоз, развивающийся при некоторых инфекционных заболеваниях (гриппе, инфекционном мононуклеозе, малярии, желтой лихорадке, брюшном тифе, вирусном гепатите, полиомиелитеи др.) также имеет иммунный характер. </p>\r\n<p>Гаптеновый агранулоцитоз возникает, когда в иммунных реакциях участвуют гаптены – вещества, сами по себе безвредные, однако при определенных условиях способные провоцировать иммунные реакции, разрушающие гранулоциты. В роли гаптенов чаще всего выступают лекарственные вещества, так что гаптеновый агранулоцитоз рассматривают, как грозное осложнение различных лечебных мероприятий. О генуинном агранулоцитозе говорят в тех случаях, когда причина резкого снижения количества гранулоцитов в крови остается неизвестной. </p>",
"diagnostics": "<p> </p>\r\n<p>Наиболее важным для подтверждения агранулоцитоза является исследование общего анализа крови и пункция костного мозга. Картина периферической крови характеризуется лейкопенией (1-2х109/л), гранулоцитопенией (менее 0,75х109/л) или агранулоцитозом, умеренной анемией, при тяжелых степенях – тромбоцитопенией. При исследовании миелограммы выявляется уменьшение количества миелокариоцитов, снижение числа и нарушение созревания клеток нейтрофильного ростка, наличие большого количества плазматических клеток и мегакариоцитов. Для подтверждения аутоиммунного характера агранулоцитоза производится определение антинейтрофильных антител. </p>\r\n<p>Всем пациентам с агранулоцитозом показано проведение рентгенографии легких, повторные исследования крови на стерильность, исследование биохимического анализа крови, консультация стоматолога и отоларинголога. Дифференцировать агранулоцитоз необходимо от острого лейкоза, гипопластической анемии. Также необходимо исключение ВИЧ-статуса</p>",
"treatment": "<p> В первую очередь необходимо устранение причинного повреждающего фактора, срочная госпитализация больного агранулоцитозом, желательно в гематологическое отделение, и помещение его в стерильные условия. </p>\r\n<p>Необходим тщательный уход за кожей и слизистыми оболочками. Подкожные и внутримышечные инъекции следует заменить внутривенными, чтобы предотвратить развитие абсцессов. </p>\r\n<p>Назначаются антибиотики широкого спектра действия, по показаниям — противогрибковые и противовирусные препараты, иммуноглобулин. Могут применяться также препараты гранулоцитарного колониестимулирующего фактора (КСФ). При некротической энтеропатии больному следует проводить парентеральное питание. </p>\r\n<p>При аутоиммунном агранулоцитозе производится угнетение аутоиммунной агрессии, больному показаны глюкокортикоиды в высоких дозах до нормализации числа гранулоцитов в крови с последующей постепенной отменой гормонов. При гаптеновом агранулоцитозе введение глюкокортикоидов не эффективно. </p>\r\n<p>При лечении цитостатического агранулоцитоза средствами выбора являются препараты рекомбинантных гемопоэтических факторов роста. </p>",
"prevention": "<p>Чтобы не допустить развитие агранулоцитоза, следует избегать контакта с фактором, способным вызвать заболевание. Во время приема цитостатиков необходим тщательный контроль показателей гемограммы (картины крови). </p>\r\n<p>Большой проблемой является профилактика повторных гаптеновых агранулоцитозов. При гаптеновых агранулоцитозах - 80% смертельных исходов, и прогноз ухудшается при повторном применении вызвавшего нейтропению лекарства. Установить, какой препарат является гаптеном, нелегко, поэтому нужно навсегда исключать из употребления все препараты, которые применялись перед появлением агранулоцитоза. </p>",
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},
"code": "D86",
"name": "Саркоидоз",
"icd_name": "Саркоидоз",
"gender": 0,
"age_min": 5,
"age_max": 94,
"cause": [
3
],
"periodicity": 1,
"slug": "d86_sarkoidoz",
"lead": "Нарушение здоровья, относящееся к группе отдельные нарушения, вовлекающие иммунный механизм",
"description": "Саркоидоз – это заболевание, при котором могут поражаться различные органы и системы (чаще всего легкие), характеризующееся образованием в пораженных тканях гранулем (ограниченные очаги воспаления, состоящие из скопления нормальных и видоизмененных клеток).",
"etiology": "<p>Этиология саркоидоза до конца не выяснена. В настоящее время существуют лишь теории возможного вклада в развитие заболевания следующих факторов:</p>\r\n<ul>\r\n<li>наследственная предрасположенность (отмечаются семейные случаи заболевания);</li>\r\n<li>инфекции, которая рассматривается не как причина развития саркоидоза, а как пусковой фактор. В качестве таких пусковых агентов обсуждаются микобактерии туберкулеза, Chlamydophila pneumoniae, Borrelia burgdorferi, отдельные виды вирусов: вирус гепатита С, вирус герпеса;</li>\r\n<li>факторов окружающей среды: вдыхание металлической пыли (пыль алюминия, бария, бериллия, кобальта, меди, золота, титана и циркония);</li>\r\n<li>курения, которое не рассматривается как непосредственная причина саркоидоза, однако у курильщиков заболевание протекает тяжелее (в большей степени снижаются функциональные возможности легких).</li>\r\n</ul>\r\n<p> </p>",
"pathogenesis": "<p>В основе патогенеза саркоидоза лежит накопление Т-лимфоцитов вследствие иммунного ответа Th-1 типа. По неизвестной пока причине активированные макрофаги и лимфоциты скапливаются в том или ином органе и продуцируют повышенное количество интерлейкинов, фактора некроза опухолей (TNF-альфа). TNF-альфа считают ключевым цитокином, участвующим в формировании гранулемы при саркоидозе.</p>\r\n<p>Развитие гранулематозной реакции связывают также с нарушениями механизмов апоптоза (запрограммированной гибели клеток) иммунокомпентентных клеток.</p>\r\n<p>Как правило, саркоидоз характеризуется полиорганным течением. Легочный саркоидоз начинается с поражения альвеолярной ткани и сопровождается развитием атипичного воспаления в легких с последующим образованием саркоидных гранулем в легких. В дальнейшем гранулема либо рассасывается, либо прорастает соединительной тканью, превращаясь в бесклеточную гиалиновую (стекловидную) массу.</p>\r\n<p>При прогрессировании саркоидоза легких развиваются выраженные нарушения вентиляционной функции, как правило, по рестриктивному типу (снижается способность легких расправляться). При сдавлении лимфатическими узлами стенок бронхов возможны обструктивные нарушения, а иногда и развитие зон гиповентиляции и спадение альвеол (ателектаз).</p>\r\n<p>Одновременно с легкими поражаются различные группы внутригрудных лимфатических узлов, которые увеличиваются за счет скопления в них множественных гранулем Саркоидные гранулемы нередко обнаруживаются в печени и селезенке, в почках. Поражение почек может приводить к почечной недостаточности.</p>\r\n<p>Кожа вовлекается в процесс гораздо реже легких и ВГЛУ, однако именно поражение кожи часто служит основной причиной обращения больных к врачу. Поражения кожи отмечаются приблизительно в 10 - 15% случаев. Выявляются мелкоузелковая, крупноузелковая, а также атипичные формы саркоидоза кожи.</p>",
"diagnostics": "<p>Диагностика саркоидоза включает:</p>\r\n<ul>\r\n<li>Сбор анамнеза (истории развития) и жалоб заболевания (расспрос о беспокоящих симптомах).</li>\r\n<li>Общий осмотр (осмотр кожных покровов, лимфатических узлов, выслушивание легких с помощью фонендоскопа).</li>\r\n<li>Общий анализ крови.</li>\r\n<li>Биохимический анализ крови.</li>\r\n<li>Туберкулиновая проба (реакция Манту) – внутрикожный тест на определение специфической чувствительности организма к микобактериям туберкулеза.</li>\r\n<li>Рентгенография органов грудной клетки, которая позволяет обнаружить увеличение внутригрудных лимфатических узлов и изменения в легких.</li>\r\n<li>Компьютерная томография органов грудной клетки.</li>\r\n<li>Спирометрия (спирография). Позволяет оценить воздушную проходимость дыхательных путей и способность легких к расправлению.</li>\r\n<li>Проба с бронходилятатором – выполнение спирометрии до и после ингаляции препарата, расширяющего бронх. Применяется для оценки обратимости сужения бронха.</li>\r\n<li>Исследование газового состава крови (определение напряжения в крови кислорода, углекислого газа, оценка насыщения крови кислородом).</li>\r\n<li>Бодиплетизмография – метод оценки функции внешнего дыхания, который позволяет определять все объемы и емкости легких, в том числе те, которые не определяются спирографией.</li>\r\n<li>Фибробронхоскопия – исследование, позволяющее осмотреть слизистую оболочку бронхов изнутри и исследовать ее клеточный состав с помощью специального аппарата.</li>\r\n<li>Биопсия легких, внутригрудных лимфатических узлов и кожных проявлений саркоидоза. Исключение составляет узловатая эритема: ее биопсия не является информативной.</li>\r\n<li>Электрокардиография (ЭКГ), холтеровское мониторирование ЭКГ, эхокардиография (ЭХО-КГ, УЗИ сердца) – для оценки функционального состояния сердца.</li>\r\n<li>Магнитно-резонансная томография (МРТ) сердца, позитронно-эмиссионная томография (ПЭТ), сцинтиграфия миокарда – редко использующиеся дорогостоящие методы, позволяющие оценить локализацию и объем поражения сердца.</li>\r\n<li>УЗИ органов брюшной полости – при их вовлечении в процесс.</li>\r\n</ul>",
"treatment": "<p>Этиотропной терапии саркоидоза не существует. Во всех случаях основной тактикой врача является сопоставление необходимости назначения лечения с тяжестью последствий от применения современной кортикостероидной, цитостатической и биологической («таргетной») терапии.</p>\r\n<p>В лечении больных саркоидозом используются средства, направленные на подавление воспалительной реакции и предотвращение фиброзной трансформации гранулем. В настоящее время наиболее эффективным средством являются кортикостероиды. Кортикостероидная терапия проводится длительно: в течение 6-8 мес.</p>\r\n<p>Используют также нестероидные противовоспалительные средства (делагил, плаквенил), антиоксиданты (тиосульфат натрия, альфа-токоферол, аскорутин), иммуномодулирующую терапию.</p>\r\n<p>Немедикаментозные методы лечения: разгрузочно-диетическая терапия, физиотерапия, плазмаферез.</p>",
"prevention": "<p>В качестве возможной меры профилактики можно рекомендовать избегать инфекционных заболеваний и контакта с металлической пылью (пыль алюминия, бария, бериллия, кобальта, меди, золота, титана и циркония).</p>\r\n<p>Для профилактики обострений саркоидоза следует стараться соблюдать здоровый образ жизни. Самое главное при поражении лёгких — не курить, так как это может привести к затруднению дыхания и осложнениям болезни. Также следует избегать лекарств и контактов с химикатами, вредными для печени, с токсичными летучими веществами, пылью, парами, газами, которые могут повреждать лёгкие. При саркоидозе наблюдается увеличение кальция в крови, что может привести к образованию камней в почках и мочевом пузыре. Поэтому следует избегать употребления продуктов, богатых кальцием. По этой же причине не следует загорать.</p>\r\n<p> </p>",
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