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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>",
"pathogenesis": "",
"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>",
"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;\">В течении пигментной ксеродермы выделяют 5 переходящих одна в другую стадий: зритематозную, стадию гиперпигментаций, атрофическую, гиперкератическую и стадию злокачественных опухолей.</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;\">Эритематозная стадия характеризуется воспалительными изменениями кожи на участках, подвергшихся воздействию ультрафиолета. В таких областях кожного покрова появляются покраснение, отек, мелкие пузырьки и пузыри. После разрешения элементов первой стадии на коже остаются коричневые, желтоватые или бурые пигментные пятна, похожие на веснушки (стадия гиперпигментаций).</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;\">Последующие облучения кожи у пациентов с пигментной ксеродермой ведут к новым воспалительным и пигментным изменениям кожи, что вызывает развитие атрофических процессов. Заболевание переходит в атрофическую стадию, для которой характерны истончение и сухость кожи, образование трещин и рубцов. Кожа натянута и не собирается в складки. Отмечается уменьшение рта (микротомия), атрезия отверстия рта и носа, истончение кончика носа и ушей.</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;\">Гиперкератическая стадия проявляется развитием в очагах пораженной кожи бородавчатых разрастаний, папиллом, кератом, фибром. Стадия злокачественных опухолей наблюдается, как правило, спустя 10-15 лет от начала пигментной ксеродермы. Но иногда злокачественные новообразования появляются в первые годы заболевания. К злокачественным опухолям, встречающимся при пигментной ксеродерме, относятся базалиомы, меланомы, эндотелиомы, саркомы, трихоэпителиомы, ангиосаркомы. Они характеризуются быстрым метастазированием во внутренние органы, приводящим заболевание к летальному исходу.</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;\">В 80-85% случаев пигментной ксеродермы наблюдаются поражения глаз в виде конъюнктивита, кератита, гиперпигментации и атрофии радужки и роговицы, приводящих к понижению зрения. На коже век появляются телеангиэктазии, гиперкератозы, дисхромии и опухолевые процессы. Нередко пигментная ксеродерма сочетается с дистрофическими изменениями тканей: дистрофией зубов, синдактилией, врожденной алопецией, отставанием в росте.</span></p>",
"image": null,
"image_alt": null,
"standard_type": 0,
"danger": 30,
"published": 1,
"parent": 7153,
"block_rubric": 185,
"standards": []
}
]
}
