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"code": "D25",
"name": "Лейомиома матки",
"icd_name": "Лейомиома матки",
"gender": 2,
"age_min": 0,
"age_max": 100,
"cause": [
3
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"slug": "d25_leyomioma_matki",
"lead": "Нарушение здоровья, относящееся к группе доброкачественные новообразования",
"description": "Это доброкачественная опухоль в полости матки, образовавшаяся вследствие деления клеток соединительных и мышечных тканей. Наиболее часто заболевание встречается у женщин среднего возраста (35-40 лет).",
"etiology": "<p>Выделяют следующие причины лейомиомы матки:</p>\r\n<ul>\r\n<li>Наследственная предрасположенность;</li>\r\n<li>Неправильный образ жизни (гиподинамия, некачественное питание);</li>\r\n<li>Различные гинекологические заболевания;</li>\r\n<li>Хирургическое или медикаментозное прерывание беременности, выкидыши;</li>\r\n<li>Гормональные сбои (повышенной продукцией эстрогена яичниками, ановуляция из-за отсутствия прогрестерона);</li>\r\n<li>Длительный прием противозачаточных препаратов (оральных контрацептивов, содержащих эстроген), внутриматочная спираль;</li>\r\n<li>Нерегулярная половая жизнь.</li>\r\n<li>Позднее начало первых менструаций;</li>\r\n<li>Скоплением в организме канцерогенных веществ, опасных добавок (усилителей вкуса, красителей, консерванты, превращающихся в эстрогены);</li>\r\n<li>Эндокринопатии (гипотиреоз, сахарный диабет);</li>\r\n<li>Избыточный вес;</li>\r\n<li>Врожденные пороки сердца и сосудов;</li>\r\n<li>Заболевания печени.</li>\r\n</ul>\r\n<p> </p>",
"pathogenesis": "<p>На сегодня патогенез миомы остается в гинекологии спорным. Одно из центральных мест в нем занимает функциональное состояние репродуктивной системы и особенности гормонального статуса при развитии заболевания. Современные исследования указывают на значимую роль эстрогенов. Это подтверждается тем, что в ткани опухоли количество рецепторов прогестерона и эстрадиола выше, чем в нормальном миометрии. В патологический процесс вовлекается и гипотоламо-гипофизарная система, что проявляется частым сочетанием миомы с дисгормональными патологиями молочных желез, а также нарушением функций щитовидной железы. Имеют значение изменения функций печени и наличие железодефицитной анемии.</p>\r\n<p> Считается, что рост узлов лейомиомы может происходить согласно трем патогенетическим вариантам – цетральному (при поражении гипоталамуса и гипофиза), маточному (при механических повреждениях эпителия при выскабливании или иных травмирующих процедурах) и яичниковому (функция яичников нарушается в случае длительного воспалительного процесса, кистозного перерождения, вследствие чего изменяется количественна секреция эстрогенов и прогестерона и их должное соотношение, самый частый вариант).</p>",
"diagnostics": "<p>В качестве диагностических процедур по назначению врача пациентакам назначаются:</p>\r\n<ul>\r\n<li>Общее гинекологическое обследование (при этом оценивается состояние половых органов, шейки матки, наличие или отсутствие рождающихся узлов, а также подвижность матки и ее размеры);</li>\r\n<li>Кольпоскопия;</li>\r\n<li>Цитологическое исследование;</li>\r\n<li>УЗИ (при этом используется трансвагинальный датчик, в результате чего нередко выявляется неуточненная миома со скрытой клиникой),</li>\r\n<li>МРТ – отчетливо видно, как при прорастании миомы во внутрибрюшинное пространство опухоль увеличивается диффузно на перитонеальных поверхностях, часто напоминая с виду злокачественную опухоль.</li>\r\n<li>Гистеросальпиногография – метод визуальной оценки опухоли, позволяющий оценить степень поражения маточной полости, узел и его размеры, поврежденность соседних органов.</li>\r\n<li>Биопсия при миоме выполняется крайне редко, лишь с целью исключения злокачественности процесса.</li>\r\n<li>Общий анализ крови с определением группы и резуса, анализ мочи, количество глюкозы в организме, биохимические анализы;</li>\r\n<li>Определение уровня гормонов и оценка состояния щитовидной железы и гипофиза.</li>\r\n</ul>",
"treatment": "<p>В начальной стадии заболевания, когда размеры опухоли не превышают 5 см, показано дечение лейомиомы матки противозачаточными таблетками (гестагенами). Благодаря снижению концентрации эстрогенов, препараты могут использоваться для уменьшения размеров опухоли в период менопаузы. Такая терапия весьма эффективна, когда цель — уменьшить миому до небольших размеров перед оперативным вмешательством.</p>\r\n<p>На сегодняшний день самым эффективным считается лечение, направленное на уменьшение объемов опухоли посредством применения гонадотропин-рилизинг-гормона аналогов, мифепристона, антагонистов прогестерона, селективных модуляторов, ингибиторов ароматазы. Несмотря на положительную динамику лечения, подобная терапия может иметь негативные последствия в виде эстроген-дефицита, остеопороза.</p>\r\n<p>Оперативное лечение</p>\r\n<p>Хирургическое удаление лейомиомы, как правило, происходит через брюшную полость, во время операции в зависимости от стадии заболевания и состояния здоровья пациентки удаляются либо фиброзные узлы либо матка полностью. Процедура миомэктомии не рекомендуется женщинам, которые не имеют детей либо выражают явное желание сохранить матку.</p>\r\n<p>При гистероскопической миомэктомии лейомиома удаляется резектоскопом, (эндоскопическим инструментом, высокочастотная электроэнергия которого направлена на сокращение тканей). Показана при подслизистой лейомиоме. Особенно эфективно использовать гистероскопическую миомэктомию при субмокозной миоме, размеры которой не превышают 5 см.</p>\r\n<p>Лапароскопическая миомэктомия выполняется путем введения лапароскопа сквозь отверстие в области пупка. Врач вставляет лапароскоп в матку и, используя хирургические инструменты, удаляет миому. Не используется при удалении миом больших размеров.</p>\r\n<p>Лапаротомная миомэктомия (она же «брюшная», «открытая») относится к инвазивным хирургическим операциям иссечения тела матки. Во время проведения процедуры доктором делается вскрытие брюшной стенки, после чего микрокатетер (не превышающий в диаметре 1 мм) вводится в бедренную артерию под местной анестезией. Изображения, выводимые на монитор, позволяют купировать обе маточные артерии, блокируя при этом приток крови к матке. Достаточно аккуратно иссечь миому, и восстановление наступает в течение нескольких дней.</p>\r\n<p>Радиочастотная абляция — одна из новейших малоинвазивных операций по устранению миомы. Техника предусматривает уменьшение миомы в размерах путем нагревания опухоли низкой частотой электрического тока через вводимое через живот игольчатое устройство. Такое лечение находится на этапе клинического тестирования и пока масово не используется в гинекологии. Процедура показана женщинам, у которых сохранена матка, которые не планируют больше в будущем беременеть и хотят избежать гистерэктомии.</p>",
"prevention": "<p>Два раза в год женщины должны обследоваться у гинеколога. Также необходимо правильно питаться, отдыхать, вести здоровый образ жизни. Профилактика включает своевременную беременность, кормление грудью, грамотное применение противозачаточных средств.</p>",
"clinical_picture": "<p>У большинства женщин симптомы лейомиомы матки отсутствуют либо слабо выражены. Если признаки болезни все же присутствуют, то обычно проявляются в виде:</p>\r\n<ul>\r\n<li>Обильных менструаций, что связано с увеличением матки (ростом эндометрия);</li>\r\n<li>Маточных кровотечений;</li>\r\n<li>Боли и тяжести внизу живота (в случае перекрута ножки узла может возникнуть острая боль в области поясницы и живота, сопровождаемая повышением температуры тела);</li>\r\n<li>Мажущих кровянистых выделений между менструациями;</li>\r\n<li>Нерегулярности менструаций;</li>\r\n<li>Кровотечениями после полового акта;</li>\r\n<li>Бесплодия;</li>\r\n<li>Резкого набора веса;</li>\r\n<li>Нарушения правильного функционирования смежных органов (частое мочеиспускание, запоры, пр.);</li>\r\n<li>Общей слабости, тяжести при ходьбе;</li>\r\n<li>Отечности;</li>\r\n<li>Варикозного расширение вен.</li>\r\n</ul>\r\n<p> </p>",
"image": null,
"image_alt": null,
"standard_type": 3,
"danger": 1,
"published": 2,
"parent": null,
"block_rubric": 37,
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},
{
"id": 8018,
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{
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"description": "",
"etiology": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">С учетом причин развития различают два типа миелодиспластического синдрома: первичный (идиопатический) и вторичный. Идиопатический вариант выявляется в 80-90% случаев, диагностируется преимущественно у пациентов старше 60 лет. Причины возникновения установить не удается. В числе факторов риска первичного миелодиспластического синдрома – курение, повышенный уровень радиации при выполнении профессиональных обязанностей или проживании в неблагоприятной экологической зоне, частый контакт с бензином, пестицидами и органическими растворителям, некоторые наследственные и врожденные заболевания (нейрофиброматоз, анемия Фанкони, синдром Дауна).</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Вторичный вариант миелодиспластического синдрома наблюдается в 10-20% случаев, может возникать в любом возрасте. Причиной развития становится химиотерапия или радиотерапия по поводу какого-то онкологического заболевания. В число лекарственных средств с доказанной способностью вызывать миелодиспластический синдром включают циклофосфан, подофиллотоксины, антрациклины (доксорубицин) и ингибиторы топоизомеразы (иринотекан, топотекан). Вторичный вариант отличается более высокой резистентностью к лечению, более высоким риском развития острого лейкоза и более неблагоприятным прогнозом.</span></p>",
"pathogenesis": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">В основе патогенеза МДС лежит воздействие повреждающих факторов на полипотентную стволовую клетку, приводящее к появлению в ней генетических аномалий, а также феномена гиперметилирования ДНК.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Указанные нарушения приводят к нарушению продукции клеток миелоидного ростка и появлению миелобластов в костном мозге и периферической крови, вследствие чего появляются диспластические изменения в зрелых клетках и их функциональная недостаточность, приводящие к описанным клиническим проявлениям.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Феномен гиперклеточности костного мозга на фоне периферической цитопении объясняется ускоренным апоптозом аномально пролиферирующих клеток костного мозга.</span></p>",
"diagnostics": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Диагноз выставляется с учетом данных лабораторных исследований: анализа периферической крови, биопсии костного мозга с последующим цитологическим исследованием, цитохимических и цитогенетических тестов. В анализе периферической крови больных миелодиспластическим синдромом обычно обнаруживается панцитопения, реже выявляется дву- или одноростковая цитопения. У 90% пациентов наблюдается нормоцитарная либо макроцитарная анемия, у 60% - нейтропения и лейкопения. У большинства больных миелодиспластическим синдромом отмечается тромбоцитопения.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">При исследовании костного мозга количество клеток обычно нормальное либо повышенное. Уже на ранних стадиях обнаруживаются признаки дизэритропоэза. Количество бластов зависит от формы миелодиспластического синдрома, может быть нормальным либо увеличенным. В последующем наблюдаются дисгранулоцитопоэз и дисмегакариоцитопоэз. У некоторых больных признаки дисплазии костного мозга выражены очень слабо. В процессе цитогенетического исследования у ¾ больных выявляются хромосомные нарушения. </span></p>",
"treatment": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Тактика лечения определяется выраженностью клинической симптоматики и лабораторных изменений. При отсутствии явных признаков анемии, геморрагического синдрома и инфекционных осложнений осуществляется наблюдение. При миелодиспластическом синдроме с выраженной анемией, тромбоцитопенией и нейтропенией, а также при высоком риске возникновения острого лейкоза назначают сопроводительную терапию, химиотерапию и иммуносупрессивную терапию. При необходимости осуществляют пересадку костного мозга.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Сопроводительная терапия является самым распространенным методом лечения миелодиспластического синдрома. Предусматривает внутривенные инфузии компонентов крови. При длительном применении может провоцировать повышение уровня железа, влекущее за собой нарушения деятельности жизненно важных органов, поэтому переливания гемокомпонентов производят при одновременном приеме хелаторов (лекарственных средств, связывающих железо и способствующих его выведению).</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Иммуносупрессоры эффективны при лечении миелодиспластического синдрома с отсутствием хромосомных аномалий, наличием гена HLA-DR15 и гипоклеточном костном мозге. Химиотерапию применяют при невозможности трансплантации костного мозга. Высокие дозы препаратов используют при трансформации миелодиспластического синдрома в острый лейкоз, а также при рефрактерных анемиях с избытком бластов при нормоклеточном и гиперклеточном костном мозге, низкие – при невозможности пересадки костного мозга. Наряду с перечисленными средствами пациентам назначают гипометилирующие средства (азацитидин). Наиболее надежным способом достижения полноценной длительной ремиссии является трансплантация костного мозга.</span></p>",
"prevention": "<p> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Всем пациентам с МДС рекомендуется постоянное динамическое наблюдение у гематолога в течение всей жизни.</span></p>",
"clinical_picture": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Основные клинические проявления миелодиспластического синдрома неспецифические и являются следствием изменения количества клеток крови. В первую очередь это цитопенический синдром, то есть совокупность состояний, вызванных снижением количества определённых клеток в периферической крови. Могут быть отдельно выделены следующие синдромы:</span></p>\r\n<ul style=\"margin-top: 0; margin-bottom: 0; padding-inline-start: 48px;\">\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">анемический синдром — возникает при снижении количества эритроцитов и\\или гемоглобина. Включает в себя бледность кожных покровов и видимых слизистых оболочек, слабость, повышенную утомляемость, раздражительность, шум или звон в ушах, головокружение, одышку, возникновение сердцебиения даже при незначительной физической нагрузке, выпадение волос, изменения ногтей (исчерченность ногтевых пластинок, принятие ими ложкообразной формы). Также могут возникать заеды в углах рта, глоссит (налёт, чувство жжения в языке, потеря вкусовой чувствительности), извращение вкуса и запаха, в ряде случаев дизурические расстройства. Встречается у подавляющего количества больных.</span></li>\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">геморрагический синдром — возникает в результате снижения количества тромбоцитов. Проявляется повышенной кровоточивостью — появлением кровоизлияний в кожу и слизистые оболочки размерами от синячков до крупных гематом, кровотечений (носовых, маточных, из дёсен, желудочно-кишечных кровотечений) и кровоизлияний во внутренние органы (головной мозг, сетчатка, суставы).</span></li>\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">лейкопения — снижение количества лейкоцитов. Поскольку лейкоциты являются основным звеном клеточного иммунитета, то присоединяются инфекции, которые и обуславливают дальнейшую симптоматику. Довольно часто, примерно в половине случаев, встречается только изолированная нейтропения — снижение количества только одного вида лейкоцитов, нейтрофилов. Кроме того, наблюдается постепенное ослабление организма, повышение температуры, озноб, учащённый пульс, беспокойство, головные боли.</span></li>\r\n</ul>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"> </p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">К иным симптомам относят:</span></p>\r\n<ul style=\"margin-top: 0; margin-bottom: 0; padding-inline-start: 48px;\">\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">инфекционные осложнения,</span></li>\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">В-симптомы (лихорадка, ночные поты, потеря веса),</span></li>\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Увеличение селезёнки,</span></li>\r\n<li><span style=\"font-size: 7pt; color: #000000; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">аутоиммунные проявления. В 10% случаев являются самыми первыми проявлениями миелодиспластического синдрома: возникает системный васкулит, некротический панникулит, серонегативный артрит, ревматическая полимиалгия, Кумбс-положительная гемолитическая анемия, перикардит, плеврит.</span></li>\r\n</ul>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">При этом нельзя не отметить, что у значительного количества больных относительно доброкачественными формами миелодиспластического синдрома долгое время может не проявляться вообще никаких симптомов, и в этом случае заболевание может быть случайной находкой, выявленной впервые при выполнении общего анализа крови.</span></p>\r\n<p><span id=\"docs-internal-guid-794b0108-7fff-3cc9-be3b-91bf47a3fd8d\"> </span></p>",
"image": null,
"image_alt": null,
"standard_type": 0,
"danger": 50,
"published": 1,
"parent": null,
"block_rubric": 38,
"standards": []
}
]
}