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"code": "Q82.0",
"name": "Наследственная лимфедема",
"icd_name": "Наследственная лимфедема",
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"lead": "постепенное увеличение объема конечности вследствие нарушения оттока лимфы и ее последующего скопления в межклеточном пространстве",
"description": "<p><span id=\"docs-internal-guid-a0c9af8d-7fff-8c0d-a415-896d754a30ab\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Наследственная лимфедема – это группа генетических патологий, которые проявляются нарушением лимфооттока от различных участков тела (чаще всего – нижних конечностей) с развитием выраженного отека.</span></span></p>",
"etiology": "<p><span id=\"docs-internal-guid-1a731fc9-7fff-ae16-1004-513393fff297\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Заболевание развивается на фоне мутации генов. В результате у больного могут развиться дисплазия лимфатических сосудов, расстройство процессов обратного всасывания жидкости, а также патология клапанов сосудов. </span></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;\">Первичный лимфостаз нижних конечностей обусловлен врожденными пороками развития лимфатической системы.</span></p>\r\n<p><span id=\"docs-internal-guid-8c1314e4-7fff-c9fc-fb8b-b928ac24c4ad\"> </span></p>",
"diagnostics": "<p><span style=\"background-color: transparent; font-family: Verdana; font-size: 7pt; white-space: pre-wrap;\">Чтобы установить и подтвердить диагноз, врач анализирует клиническую картину, изучает семейную историю болезни, проводит физикальный осмотр и направляет пациента на дополнительные обследования. </span></p>\r\n<p><span style=\"background-color: transparent; font-family: Verdana; font-size: 7pt; white-space: pre-wrap;\">В целях диагностики выполняют ультразвуковую допплерографию, компьютерную томографию, лимфангиографию и молекулярно-генетические исследования, методом секвенирования генов GJC2 и VEGF3. </span></p>\r\n<p><span style=\"background-color: transparent; font-family: Verdana; font-size: 7pt; white-space: pre-wrap;\"> </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;\">Терапия наследственной лимфедемы сводится к нескольким принципам – улучшению оттока лимфы, снижению задержки тканевой жидкости и устранению вторичных нарушений, обусловленных отечным синдромом. </span></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;\">Для улучшения оттока применяют разнообразные лимфодренажные массажи (как ручные, так и аппаратные) и особый компрессионный трикотаж, иногда используют местные лекарственные средства. </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;\">Для некоторых форм наследственной лимфедемы могут быть эффективными хирургические методики, создающие более полноценные пути эвакуации тканевой жидкости в лимфатическую или кровеносную системы. </span></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;\">Для снижения задержки лимфы в тканях назначают специальные диеты с пониженным содержанием белков и солей – эти нутриенты способны значительно усугублять течение лимфатического отека.</span></p>\r\n<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;\">При запущенных формах наследственной лимфедемы с выраженными вторичными нарушениями (слоновостью, трофическими язвами, инфекцией) проводят лечение осложнений. Для борьбы с инфекцией назначают антибиотики, трофические нарушения лечат при помощи витаминотерапии, регенеративных средств и биогенных стимуляторов. При выраженной слоновости иногда производится хирургическое удаление лишнего объема тканей (резекционное оперативное вмешательство), что приводит к улучшению как внешнего вида, так и состояния больного наследственной лимфедемой.</span></p>",
"prevention": "<p><span id=\"docs-internal-guid-5b5d8d0f-7fff-dcec-1082-a6276ac506b5\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Специфические методы профилактики не разработаны. Парам, планирующим беременность, рекомендована консультация генетика. </span></span></p>\r\n<p><span id=\"docs-internal-guid-5b5d8d0f-7fff-dcec-1082-a6276ac506b5\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Если у пациента выявлена наследственная лимфедема, ему необходимо соблюдать диету, отказаться от длительных физических нагрузок на конечности, а также придерживаться медицинских рекомендаций.</span></span></p>",
"clinical_picture": "<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;\">Первичная лимфедема развивается из-за врожденной аплазии или гипоплазии лимфатических сосудов.</span></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;\">Компенсированная первичная лимфедема нередко быстро прогрессирует после беременности или травмы. </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;\">Жалобы: боли, слабость, ощущение распирания, тяжесть в пораженной конечности, ограничение подвижности суставов. Кожные покровы в пораженной области бледные, рисунок сети подкожных вен не определяется, кожная складка утолщена. Вначале поражаются дистальные отделы конечностей (стопы или кисти). </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;\">Припухлость может быть уже при рождении, но обычно появляется позже, по мере того как объем лимфы увеличивается и превышает возможности малого количества лимфатических сосудов. У пациентов появляется безболезненный плотный отек пальцев, распространяющийся на стопу и голеностопный сустав (при поражении верхней конечности – на кисть и лучезапястный сустав). Постепенно отек распространяется на голень и бедро. Ноги больного становятся похожими на колонны. В области суставов со временем образуются складки из отечных мягких тканей. Складки на тыле стопы не выражены. Кожа напоминает апельсиновую корку. </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;\">Наследственная лимфедема со временем не исчезает полностью даже после ночного отдыха. Нарушается питание тканей. Возникают участки гиперкератоза. Измененная кожа трескается, появляются язвы. Иногда развиваются лимфатические свищи между пальцами. Часто осложняется рожистым воспалением, которое может стать причиной флегмоны, вызывает облитерацию сохранных лимфатических сосудов и приводит к быстрому прогрессированию заболевания.</span></p>",
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"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;\">Пигментная ксеродерма — генетическое заболевание, которое передается рецессивным геном от родителей к детям. Патология имеет семейный характер, довольно часто наблюдается при близкородственных браках. Как правило, данную генетическую патологию отмечают у изолятов — обособленных человеческих популяций.</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;\">В этиологии дерматологической патологии лежит наследственно обусловленный дефицит ферментов УФ-эндонуклеазы, полимеразы-1, которые принимают активное участие в восстановлении ДНК после ее повреждения УФ-лучами. Недуг передается аутосомно-доминантным или аутосомно-рецессивным путем.</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;\">В организме больного человека полностью отсутствуют ферменты, которые нейтрализуют вредное воздействие ультрафиолета на эпидермис. При этом под воздействием УФ-лучей в структурах дермы накапливаются мутирующие клеточные структуры, что приводит к развитию рака кожи.</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;\">Чрезмерная инсоляция, длительное пребывание на солнце провоцируют развитие и обострение пигментной ксеродермы</span></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;\">Помимо УФ-излучения, причиной ксеродермы является ионизирующее излучение, солнечная радиация.</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;\">Факторы, причины пигментной ксеродермы:</span></p>\r\n<ul>\r\n<li><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;\">врожденные генетические аномалии аутосомно-рецессивного характера;</span></li>\r\n<li><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;\">повреждение ферментов УФ-эндонуклеазы;</span></li>\r\n<li><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;\">разрушение ДНК- РНК-полимеразы;</span></li>\r\n<li><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;\">повреждение экзонуклеазы;</span></li>\r\n<li><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;\">увеличение концентрации в кровеносном русле пигментов порфиринов;</span></li>\r\n<li><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;\">интенсивное воздействии радиации, УФ-облучения с длиной волн от 260 до 330 нм.</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;\">Как правило, в 70% развитие дерматологической патологии приходится на первые годы жизни, поэтому ксероз кожи у детей диагностируют в возрасте двух-трех лет. Реже ее отмечают у пациентов после 25-35 лет. Случаи более позднего развития и проявления болезни в традиционной медицине встречаются крайне редко.</span></p>\r\n<p> </p>",
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"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;\">Специфический метод диагностики пигментной ксеродермы проводится при помощи монохроматора и заключается в выявлении повышенной чувствительности кожного покрова к воздействию ультрафиолета.</span></p>\r\n<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;\">Для уточнения диагноза дерматолог назначает биопсию пораженного участка кожи. Последующее гистологическое исследование в ранней стадии заболевания определяет гиперкератоз, отек и воспалительную инфильтрацию дермы, истончение росткового слоя, пигментацию базального слоя. В атрофической и гиперкератической стадии наблюдается атрофия эпидермиса, дегенеративные изменения коллагеновых и эластических волокон. В стадии злокачественных опухолей — атипические клетки и гистологическая картина рака кожи.</span></p>",
"treatment": "<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;\">Пациентам следует избегать воздействия УФ-лучей: носить шляпы с большими полями и вуали, применять солнцезащитные крема и мази, использовать пудры с танином. Медикаментозное лечение пигментной ксеродермы в основном симптоматическое и, к сожалению, малоэффективно. Применяют ароматические ретиноиды, токоферол, хингамин. При развитии злокачественных процессов дополнительно назначают проспидин, пиридоксин, тиамин, цианокобаламин. Папилломатозные и бородавчатые разрастания удаляют хирургически, путем криодеструкции, электрокоагуляции или удаления лазером.</span></p>",
"prevention": "<p>Профилактических мер не разработано.</p>",
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"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;\">К мастоцитозу приводит избыточное накопление тучных клеток. Тучные клетки – это разновидность лейкоцитов, которые играют важнейшую роль в развитии воспаления и аллергических реакций. Когда есть такая угроза для организма, например, инфекция, аллерген или токсин - происходит выделение специальных медиаторов – биологически активных веществ, которые включают в организме защитную реакцию. Например, одни из таких «защитников» является гистамин, который запускает аллергическую реакцию немедленного тип: зуд, отёк и покраснения.</span></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;\">Мастоцитоз вызывает избыток тучных клеток, которые патологически размножаются и накапливаются в тканях и органах. Почему это происходит до сих пор до конца неизвестно.</span></p>\r\n<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;\">Триггерными факторами развития мастоцитоза могут быть любые причины, которые в состоянии вызвать аллергическую реакцию, в том числе стресс, холод, жара, избыток ультрафиолета. Чрезмерное количество тучных клеток приводит к выбросу большого количества медиаторов, гистамина в том числе.</span></p>",
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"diagnostics": "<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;\">Диагноз мастоцитоз устанавливается на основании симптомов и жалоб пациента, результатов лабораторных и инструментальных (УЗИ, рентгенография, КТ), диагностических исследований, биопсии костного мозга, биопсии кожи или органов (по показаниям), генетического тестирования. Таким образом определяется уровень тучных клеток и выделяемых ими веществ (триптазы, гистамина, лейкотриенов, простагландина), степень и стадия заболевания. Основным диагностическим критерием является наличие многоочаговой инфильтрации тучными клетками костного мозга, тканей и органов.</span></p>",
"treatment": "<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;\">В лечении мастоцитоза применяют хлоргидрат ципрогептадина, ингибиторы серотонина, противоаллергические препараты (лемастин, цетиризин, фексофенадин), противовоспалительные (диклофенак, ибупрофен), ПУВА-терапию. При системном мастоцитозе назначают цитостатики, при буллезных проявлениях — кортикостероиды. Отдельные мастоцитомы могут быть удалены хирургически.</span></p>",
"prevention": "<p><span id=\"docs-internal-guid-c8758ebe-7fff-9907-529c-711694f44e50\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Профилактика мастоцитоза заключается в предотвращении воздействия на организм активаторов дегрануляции тучных клеток, таких как простуда, воздействие холода, тепла, травма, инсоляция, лекарственные препараты (особенно морфино-опиумная группа алкалоидов и ацетилсалициловая кистота).</span></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;\">Мастоцитоз может быть агрессивным и вялотекущим. Люди гораздо чаще болеют медленными, вялотекущими формами мастоцитоза. Симптомы бывают кожными и системными.</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;\">Кожные симптомы</span></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;\">Основное проявление болезни — типичная сыпь и аллергоподобные проявления, например, зуд, отёк и покрасненияе. Пятен бывает немного, но иногда они покрывают всё тело.</span></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;\">Отличительная особенность сыпи — реакция на трение (симптом Дарье — Унны). Если потереть пятно, то оно становится ярко-красным, отекает, появляется волдырь, но с течением времени всё само проходит. Симптом Дарье — Унны есть практически у всех пациентов с мастоцитозом.</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;\">Системные симптомы</span></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 мастоцитозе возможны следующие системные проявления:</span></p>\r\n<ul>\r\n<li><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;\">Симптомы анемии — слабость, бледность, одышка, учащённое сердцебиение даже при лёгкой нагрузке.</span></li>\r\n<li><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;\">Симптомы поражения костей — боли в спине как при радикулите. Возможны переломы из-за снижения минеральной плотности костей и развития остеопороза. До 40 % пациентов с мастоцитозом страдают от симптомов поражения костей.</span></li>\r\n<li><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;\">Симптомы увеличения печени и селезёнки — слабость, недомогание, боль в боках, асцит (брюшная водянка). При асците живот увеличен, вздут, кожа на животе натянута.</span></li>\r\n<li><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;\">Желудочно-кишечные симптомы — неприятные ощущения в животе, изжога, тошнота, рвота, жидкий стул (диарея).</span></li>\r\n<li><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;\">Анафилактический шок. Это одно из самых опасных проявлений мастоцитоза. Сопровождается резким снижением артериального давления. Человек при этом ощущает выраженную слабость, головокружение, иногда теряет сознание и может получить травму при падении. 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