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"code": "D22",
"name": "Меланоформный невус",
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"lead": "кожное образование из видоизмененных клеток кожного пигмента меланина",
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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;\">Меланоформный невус туловища или других частей тела появляется под воздействием нескольких факторов. При перемещении меланобластов из нейроэктодермальной трубки в меланоциты происходят нарушения, вследствие чего происходит скопление меланина в одной зоне. Так возникают невусы врожденным путем. При этом такие образования у ребенка остаются незаметными. Их наличие на теле определяется с возрастом. Риск появления признаков перерождения доброкачественных новообразований в злокачественные опухоли выше, если невусы занимают большую площадь тела.</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;\">Приобретенные меланоформные невусы появляются по разным причинам. К самым распространенным факторам, вызывающим развитие новообразований на теле, относятся:</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;\">длительное нахождение под солнечными лучами;</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;\">частые кожные заболевания;</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;\">изменения на гормональном уровне, к примеру, при беременности.</span></li>\r\n</ul>",
"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;\">Ранняя диагностика способна не только выявить вид меланоформного образования, но и первые признаки развития меланомы. Для исследования используются следующие виды диагностики:</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;\">люминесцентная микроскопия (исследует клетки новообразования);</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;\">компьютерная диагностика (посредством данного метода можно установить точное строение невуса, а, значит, поставить точный диагноз и назначить курс лечения);</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;\">анализ крови (для выявления онкомаркеров).</span></li>\r\n</ul>",
"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;\">Большинство приобретённых невусов на протяжении всей жизни остаются доброкачественными и требуют только наблюдения. Однако пациентам с множественными невусами следует раз в год или чаще проходить осмотр всего тела и консультироваться по поводу защиты от солнца.</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;\">Приобретённые меланоцитарные невусы удаляют в следующих случаях:</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;\">если они расположены на подошве или ладонях, имеют пятнистую пигментацию или диаметр более 5 мм;</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;\">образовались в матриксе ногтя, имеют вид отдельных полос тёмного цвета или шириной более 4 мм;</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;\">имеют выраженный асимметричный контур, участки розового или красного цвета или окрашены в несколько оттенков;</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;\">быстро растут, меняют цвет или структуру;</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;\">выделяются среди других невусов на теле, например имеют другой цвет.</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;\">Также следует удалять гало-невусы, центральная часть которых имеет нетипичные черты, и невус Шпитц с атипичными признаками: диаметром более 1 см, асимметрией и изъязвлением.</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;\">Волоски в структуре невуса не доказывают его доброкачественность. Невусы удаляют, если есть атипичные признаки, независимо от наличия или отсутствия волос. Показанием к удалению может также служить косметический дискомфорт и постоянная травматизация участка, где расположен невус.</span></p>",
"prevention": "<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;\">Специфических мер, которые могут предотвратить появление невусов, не существует.</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;\">Единственный управляемый фактор — это воздействие УФ-излучения. Чтобы контролировать его, нужно:</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;\">не находиться под прямыми солнечными лучами днём, с 10 до 16 часов;</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;\">использовать солнцезащитный крем с высокой степенью защиты (SPF 30+);</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;\">надевать солнцезащитную одежду, в том числе головные уборы с широкими полями, закрывающими лицо, шею и уши;</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;\">использовать очки с защитой от ультрафиолета;</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;\">не применять солнечные лампы и не посещать солярий.</span></li>\r\n</ul>",
"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;\">Меланоцитарный невус — это хорошо отграниченное, круглая или овальная опухоль кожи, обычно, имеющая размеры от 2 до 6 мм в диаметре. Хотя, множество невусов имеют небольшую асимметрию, границы, обычно, правильные и хорошо определимы. </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;\">Пограничный меланоцитарный невус — это образование в виде пятна с небольшим усилением кожного рисунка, заметным при боковом освещении. Пограничный меланоцитарный невус также характеризуется однородной коричневой или темно-коричневой окраской. </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;\">Сложный меланоцитарный невус выступает на различную высоту, имеет слегка более светлую окраску, чем пограничный. </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;\">Внутридермальный меланоцитарный невус, обычно, больше возвышается и более светлой окраски, чем сложный невус, иногда, даже телесного цвета. Тем не менее, необходимо подчеркнуть, что существует клиническая и дерматоскопическая схожесть между всеми тремя типами обычных меланоцитарных невусов. Внутридермальный меланоцитарный невус в большей степени, чем сложный, имеет форму куполообразной шишки или папилломы. Интрадермальный невус или сложный могут напоминать себорейный кератоз своей бородавчатой поверхностью. </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;\">Многие невусы имеют более жесткие и темные волосы по сравнению с волосами на окружающей коже. </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;\">Меланоцитарный невус на ладони и подошве часто выглядит как темное пятно и лишь слегка возвышается, имеет правильные, хорошо определимые края и однородную коричневую окраску. </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;\">Невус ногтевого ложа представлен однородно окрашенной светло или темно-коричневой продольной полосой с правильными различимыми границами. </span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Важным аспектом меланоцитарного невуса является отношение с меланомой. Значительный процент пациентов с меланомой сообщают о длительном присутствии меланоцитарного невуса на участке кожи, где впоследствии развилась меланома. Гистологические исследования находят остатки меланоцитарного невуса в трети удаленных меланом. Повышенное количество меланоцитарных невусов означает повышенный риск меланомы. В большей степени это утверждение относится к диспластическим разновидностям.</span></p>",
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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>",
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"standard_type": 3,
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}
]
}
