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},
"code": "B05",
"name": "Корь",
"icd_name": "Корь",
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"lead": "острое инфекционное заболевание, характеризующееся воспалением слизистых оболочек дыхательных путей, глаз, пятнисто-папулезной сыпью, общей интоксикацией",
"description": "<p>Корь - острая высококонтагиозная инфекционная болезнь, которая вызывается вирусом кори, передается воздушно-капельным путем, характеризуется двухволновой лихорадкой, катаральным воспалением слизистых оболочек дыхательных путей, глаз, наличием пятен Бельского-Филатова-Коплика, а с новым повышением температуры тела - этапным возникновением на теле характерной пятнисто-папулезная экзантема, что оставляет пигментацию</p>",
"etiology": "<p>Возбудитель кори - Morbillivirus - принадлежит к роду Morbillivirus, семьи Paramyxoviridae, содержит РНК, но, в отличие от других парамиксовирусов, в его состав не входит нейраминидаза. Известен лишь один антигенный тип вируса. Вирион диаметром 120-180 нм, овальной формы. Антигены оболочки вируса имеют гемаглютинуючи, гемолизирующая, комплементсвязывающие свойства и вызывают образование в организме вируснейтрализующим антител. Репродуцируется в первично-трипсинизованих культурах почечных клеток человека и обезьян, а также после адаптации в других культурах. Вирус нестоек к факторам внешней среды. При комнатной температуре он погибает через несколько часов, подвержен воздействию высоких температур, УФО и дезинфицирующих средств.</p>\r\n<p>Источником инфекции являются больные. Максимальная заразительность наблюдается в течение катарального периода и в первый день сыпи. Инфицированный человек становится опасным для окружающих на 9-10-й день после контакта, а в некоторых случаях - с 7-го дня. С 3-го дня сыпи выделения вируса во внешнюю среду, а соответственно и контагиозность больного резко снижаются и с четвертого дня от начала высыпаний больной считается незаразным.<br />Механизм передачи кори - воздушно-капельный. Вирус выделяется в большом количестве во внешнюю среду с капельками слизи при кашле, чиханье и со струей воздуха может переноситься на значительные расстояния - в другие помещения, этажи. Индекс контагиозности при кори составляет 95-96%, т.е. на него заболевают 95-96% восприимчивых людей, которые были в контакте с больным, независимо от их возраста. До применения противокоревой вакцины вспышки болезни наблюдались каждые два - четыре года. Периодические повышения заболеваемости объясняются наличием достаточного количества восприимчивых детей. В связи с вакцинацией корью болеют преимущественно подростки и молодые лица, которым она не проводилась, а также дети, привитые в возрасте до 12 месяцев.<br />Заболеваемость регистрируется в течение года, но максимальное ее повышение наблюдается в осенне-зимний и весенний периоды.<br />После перенесенной кори формируется стойкий пожизненный иммунитет, после митигованого - менее устойчив. Повторные случаи заболевания наблюдаются редко (2-4%). Младенцы до 3-4 месяцев, получивших пассивный иммунитет от матери, не болеют. Через 9 месяцев после рождения материнские антитела в крови ребенка практически не проявляются, однако и в этом возрасте у нее сохраняется некоторая невосприимчивость к кори.</p>",
"pathogenesis": "<p>Проникновение вируса в организм человека происходит через слизистую оболочку верхних дыхательных путей и далее с током крови (первичная виремия) вирус попадает в ретикулоэндотелиальную систему (лимфатические узлы) и поражает все виды белых кровяных клеток. С 3-го дня инкубационного периода в лимфоузлах, миндалинах, селезенке можно обнаружить типичные гигантские многоядерные клетки Warthin-Finkeldey с включениями в цитоплазме. После размножения в лимфатических узлах вирус снова попадает в кровь, развивается повторная (вторичная) вирусемия, с которой связано начало клинических проявлений болезни. Вирус кори подавляет деятельность иммунной системы (возможно непосредственное поражение Т-лимфоцитов), происходит снижение иммунитета и, как следствие, развитие тяжелых вторичных, бактериальных осложнений с преимущественной локализацией процессов в органах дыхания. Вирус, возможно, вызывает и временный гиповитаминоз витамина А.</p>\r\n<p>Микроскопическая картина: слизистая дыхательных путей — <a title=\"Перейти на страницу симптома Отёк\" href=\"/symptom/otek/\">отёк</a>, полнокровие сосудов, очаги некроза, участки метаплазии эпителия, очаговая лимфогистиоцитарная инфильтрация в подслизистом слое. Ретикулоэндотелиальная система — клетки Warthin-Finkeldey. Кожа — изменения в сосочковом слое дермы в виде отёка, полнокровия сосудов, кровоизлияний с периваскулярной лимфогистиоцитарной инфильтрацией, фокусы некроза в эпидермисе.</p>",
"diagnostics": "<p>В катаральном периоде корь надо дифференцировать с гриппом, другими ОРВИ. Диагноз устанавливается при наличии пятен Бельского-Филатова-Коплика, которых при гриппе и других ОРВИ нет.<br />В случае наличия продромального скарлатиноподобная сыпи, равномерно покрывает кожу, следует проводить дифференциальную диагностику со скарлатиной. Для нее катаральные проявления совершенно нетипичные, а <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">сыпь</a> располагается преимущественно на сгибательных поверхностях со скоплением в местах естественных складок. Данные эпидемиологического анамнеза и выявления пятен Бельского-Филатова-Коплика окончательно решают вопрос в пользу кори.<br />В период <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">высыпания</a> корь нужно дифференцировать с краснухой, инфекционной эритемой, энтеровирусной экзантемой, разнообразной кореподобной сыпью.<br />У больных краснухой катаральный период зачастую отсутствует. <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">Сыпь</a> появляется в первый день болезни и в течение нескольких часов распространяется на все туловище и конечности. Присущей для кори этапности <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">высыпания</a> нет. <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">Сыпь</a> мелко-пятнистый, розовый, гладкий, не сливается, располагается преимущественно на разгибательных поверхностях конечностей, спине, ягодицах, не оставляет пигментации и шелушения. Слизистые оболочки трубы при краснухе блестящие, обычной окраски. Типичным является увеличение и болезненность лимфатических узлов, особенно затылочных и заднешейных.<br />Инфекционная <a title=\"Перейти на страницу симптома Покраснение кожи\" href=\"/symptom/pokrasnenie_kozhi/\">эритема</a> Розенберга-Чамера отличается от кори наличием в 1-2-й день болезни пятнисто-папулезная <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">сыпь</a>, который на щеках и спинке носа сливается, напоминает по форме бабочку. <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">Сыпь</a> можно обнаружить на конечностях, больше в проксимальных отделах (плечи, бедра) и на разгибательных поверхностях, реже - на туловище. <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">Сыпь</a> яркий, группируется в кольца, гирлянды, бледнеет по центру.</p>\r\n<p>В дифференциальной диагностике кори с энтеровирусной экзантемой учитывается эпидемиологический анамнез, отсутствие продромального периода, пятен Бельского-Филатова-Коплика и этапности высыпаний.<br />Сывороточная болезнь сопровождается кореподобной сыпью и развивается через 7-10 дней после введения чужеродной сыворотки крови. <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">Сыпь</a> начинается с места введения сыворотки, образуются уртикарных элементов, выраженный <a title=\"Перейти на страницу симптома Зуд\" href=\"/symptom/zud/\">зуд</a>. Наблюдаются <a title=\"Перейти на страницу симптома Отек тканей\" href=\"/symptom/otek_tkaney/\">припухлость</a> и болезненность суставов, увеличение периферических лимфатических узлов. Есть катаральных проявлений и этапности высыпаний. Кореподобная <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">сыпь</a> может появиться вследствие применения сульфаниламидных препаратов, антибиотиков и т.п.. Основные признаки медикаментозной экзантемы - это отсутствие коревой триады Стимсона, иногда - температурной реакции, этапности высыпаний, интактнисть слизистой оболочки рта, <a title=\"Перейти на страницу симптома Зуд\" href=\"/symptom/zud/\">зуд</a> кожи, изменчивость элементов сыпи, преимущественная локализация его вокруг суставов.<br />Для синдрома Стивенса-Джонсона характерно некротично-язвенные поражения слизистой оболочки вокруг естественных отверстий (глаз, рта, носа, половых органов, заднего), наряду с кореподобной элементами появляются большие буллезные.<br />Во всех случаях при установлении диагноза учитывается периодичность фаз инфекционного процесса, присущее кори наличие пятен Бельского-Филатова-Коплика в катаральном периоде и этапность высыпаний.</p>",
"treatment": "<p style=\"padding-bottom: 19px;\" align=\"justify\">Корь лечат амбулаторно, госпитализируют больных с тяжелым осложненным течением, либо по эпидемиологическим показаниям.</p>\r\n<p style=\"padding-bottom: 19px;\" align=\"justify\">Постельный режим назначается на весь лихорадочный период. Достаточно эффективной этиотропной терапии в настоящее время не разработано, лечение заключается в облегчении симптоматики и предупреждении осложнений. В качестве меры, снижающей токсикоз, рекомендуют обильное питье. Интенсивные дезинтоксикационные мероприятия производятся в случаях крайне тяжелого течения.</p>\r\n<p style=\"padding-bottom: 19px;\" align=\"justify\">Больным необходимо соблюдать гигиену рта и глаз, избегать яркого света. В качестве патогенетической и симптоматической терапии назначают антигистаминные, жаропонижающие средства, витамины и адаптогены. В ранние сроки заболевания заметно улучшает течение прием интерферона. В случае угрозы возникновения вторичной инфекции, назначают антибиотики широкого спектра действия. Коревый энцефалит требует назначения высоких доз преднизолона и других мер интенсивной терапии.</p>",
"prevention": "<p style=\"margin-top: 10px; margin-bottom: 10px;\">Для снижения заболеваемости применяют неспецифическую и специфическую профилактику. Неспецифические меры – изоляция больных от начала продромальных проявлений до 5 дня с момента появления сыпи, возможно до 10 дня при наличии осложнений со стороны дыхательных путей. Контактные лица изолируются до 21 дня. Но люди, перенесшие в прошлом корь или вакцинированные карантинизации не подлежат и профилактические мероприятия среди них не распространяются.</p>\r\n<p style=\"margin-top: 10px; margin-bottom: 10px;\">Специфические мероприятия: активная профилактика: вакцинация ЖКВ (вакцина «Рувакс» или MMR) в возрасте 12 месяцев, а потом в 6 лет. Или же пассивная - введение Y-глобулина не позднее 3-5 дня от возможного контакта и, не менее 3 мл для предотвращения заболевания.</p>",
"clinical_picture": "<p>Инкубационный период длится в среднем около 1-2 недель.</p>\r\n<p>Затем вирус проникает в кровь из слизистой оболочки рта и глотки и распространяется практически во все органы и ткани.</p>\r\n<p>Начинается корь с:</p>\r\n<ul>\r\n<li>вялости;</li>\r\n<li>головной боли, снижения аппетита;</li>\r\n<li>насморка с обильными слизистыми (белыми) или слизисто-гнойными (желто-зелеными) выделениями;</li>\r\n<li>сухого, «лающего» кашля;</li>\r\n<li>осиплости <a title=\"Перейти на страницу симптома Слуховые галлюцинации\" href=\"/symptom/sluhovye_gallyucinacii/\">голоса</a>;</li>\r\n<li>коньюктивита (глаза красные и слезятся). Больной жалуется резь в глазах, его раздражает яркий свет;</li>\r\n<li>повышения температуры до 39,0 С и выше.</li>\r\n</ul>\r\n<p>На 3-5 день самочувствие больного несколько улучшается, снижается температура. Однако через день температура вновь повышается. На внутренней поверхности щек образуются характерные пятна, напоминающие скопление зерен манной крупы.</p>\r\n<p>Через два дня развивается типичное проявление кори – <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">сыпь</a>. <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">Сыпь</a> состоит из мелких папул (волдырей), окруженных пятном; она мелкая и обильная, яркая; способна, сливаясь, покрывать всю поверхность тела, в тяжелых случаях на коже образуются мелкие кровоизлияния.</p>\r\n<p>Этапность высыпаний</p>\r\n<p>Характерно для коревой сыпи: </p>\r\n<ul>\r\n<li>В первый день они появляются за ушами, на волосистой части головы, лице и шее;</li>\r\n<li>На второй день — на туловище и верхней части рук;</li>\r\n<li>На третьи сутки - на ногах и нижней части рук. В тоже время на лице элементы сыпи бледнеют. </li>\r\n<li>С четвертого дня <a title=\"Перейти на страницу симптома Сыпь\" href=\"/symptom/syp/\">высыпания</a> продолжают бледнеть в том же порядке, что и появились, оставляя за собой <a title=\"Перейти на страницу симптома Шелушение кожи\" href=\"/symptom/shelushenie_kozhi/\">шелушение</a> и <a title=\"Перейти на страницу симптома Пятно на коже\" href=\"/symptom/pyatno_na_kozhe/\">потемнение кожи</a> (пигментацию).</li>\r\n</ul>",
"image": "http://api.symptomd.ru/storage/9034a4e04d7cde34324af9c17ecac699_IpXO5p5.png",
"image_alt": "Корь",
"standard_type": 1,
"danger": 50,
"published": 1,
"parent": null,
"block_rubric": 11,
"standards": [
5022,
5023,
5059
]
},
{
"id": 8436,
"symptoms": [],
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"complications": [],
"medicine_branches": [],
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},
{
"id": 15430,
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"disease": 6103
}
],
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"code": "B40",
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"lead": "группа хронических, неконтагиозных глубоких микозов, которые вызываются дрожжевыми и дрожжеподобными грибами",
"description": "<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;\">Бластомикоз – это системная болезнь, относящаяся к категории микозов, поражающая первичную дегенерацию легочной ткани и проникновение грибковой инфекции во все органы и их системы.</span></p>",
"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;\">Североамериканский бластомикоз вызывается диморфным (двухфазным) сапрофитирующим грибом Blastomyces dermatitidi, обитающим в почве. В организм человека гриб попадает воздушно-пылевым путем при вдыхании спор грибка с частицами пыли. К основным путям распространения возбудителя в организме относятся гематогенный и лимфогенный. Возможен половой путь передачи бластомикоза. Возбудитель бластомикоза может существовать в двух формах: мицелиальной и дрожжевой. В мицелиальной форме гриб существует при температуре ниже 30°С, а в пораженном организме (при t 37°С) он переходит в дрожжевую фазу.</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;\">Попав в легкие, микроконидии гриба переходят в дрожжевую фазу и вызывают развитие первичных инфильтративных очагов воспаления. На более поздних стадиях в очагах формируются гранулемы с участками нагноения и некроза. Поражение кожи и внутренних органов носит вторичный характер и возникает вследствие заноса инфекции из легких. Развитию бластомикоза способствуют сопутствующие заболевания: сахарный диабет, туберкулез, болезни крови, иммунодефицитные состояния (например, ВИЧ-инфекция). К группам риска по заболеваемости бластомикозом относятся садоводы, сельскохозяйственные рабочие и другие люди, часто контактирующие с почвой, содержащей споры бластомицетов, а также лица, проживающие в эндемичных районах.</span></p>",
"pathogenesis": "<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;\">Микроконидии попадают в легкие, где развиваются первичные очаги воспаления. Микроконидии трансформируются в дрожжевые клетки крупных размеров. При формировании гранулемы выявляются участки нагноения и некроза, соседствующие с неповрежденными тканями. Выраженные процессы альтерации предопределяют массивность выделения гриба с патологическим материалом. Имеют место случаи первичного бластомикоза кожи, развившегося после травмы. Развитию микоза способствуют сахарный диабет, туберкулез, гемобласты, иммупосупрессивные состояния; у таких лиц бластомикоз проявляет склонность к диссемииации. Диссеминированная (системная) форма заболевания может развиться спустя несколько лет после первичного легочного поражения. В патологический процесс могут извлекаться любые органы, но чаще поражаются кожа, кости, органы мужской мочеполовой системы, надпочечники.</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;\">Прежде всего, бластомикоз следует заподозрить у больных, прибывших из эндемичных районов и имеющих признаки поражения легких, кожи, костей, мочеполовой системы. Поэтому к обследованию таких больных, кроме узких специалистов (пульмонолога, дерматолога, уролога и др.), должны привлекаться инфекционисты и микологи.</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;\">Диагноз бластомикоза подтверждается при обнаружении B. dermatitidi в биологическом материале: мокроте, гнойном отделяемом из свищей и абсцессов, моче, ликворе, биопсийном материале. Чаще всего применяется микроскопическое исследование и микробиологический посев. Для получения образцов материала осуществляется пункция абсцессов и аспирация их содержимого, эксцизионная биопсия тканей. Серологическая диагностика бластомикоза проводится методами ИФА, РСК, РИА. Кожно-аллергические пробы с бластомицином обладают низкой чувствительностью и специфичностью. С целью выявления изменений во внутренних органах проводятся дополнительные инструментальные исследования: рентгенография грудной клетки, остеосцинтиграфия, КТ головного мозга и позвоночника.</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;\">Острый легочный бластомикоз может закончиться выздоровлением без специального лечения. Во всех остальных случаях основу лечения различных форм бластомикоза составляют противогрибковая терапия. При легком течении заболевания назначается итраконазол или кетоконазол внутрь в течение 6 месяцев; при тяжелых - амфотерицин В внутривенно капельно. По показаниям противогрибковая терапия дополняется хирургическими методами – дренированием плевральной полости, вскрытием абсцессов кожи, некрэктомией и др.</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;\">Адекватная и своевременная терапия локализованных форм бластомикоза позволяет достичь выздоровления в 90% случаев. При диссеминированных формах в отсутствии лечения высока вероятность летального исхода. </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;\">Во избежание заражения бластомикозом рекомендуется соблюдение правил личной гигиены, защита органов дыхания при рыхлении почвы и проведении других сельхозработ в неблагополучной местности, использование барьерных методов контрацепции при случайных половых контактах.</span></p>",
"clinical_picture": "<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-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Различают следующие клинические формы бластомикоза: легочную, кожную, костную, мочеполовую и прочие (поражения ЦНС, перикарда, печени, селезенки, щитовидной железы, надпочечников). Системный (диссеминированный) бластомикоз может развиться спустя годы после первичного поражения легких.</span></p>\r\n<p><span><span> </span></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-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Легочная форма бластомикоза составляет 60–90% всех случаев грибковой инфекции и протекает в форме бронхопневмонии. Инкубационный период в среднем занимает 30–45 дней. Начало заболевания острое или подострое; в начальном периоде превалирует интоксикационный синдром: субфебрильная или фебрильная температура, озноб, мышечные и суставные боли. Реже бластомикоз с самого начала развивается как первично-хронический, без выраженной клинической симптоматики. Беспокоит кашель (вначале сухой, затем с гнойной мокротой), кровохарканье, боли в грудной клетке, одышка. При объективном исследовании выслушиваются хрипы, шум трения плевры; рентгенологически выявляются верхнедолевые инфильтраты, иногда – каверны. Для окружающих больные с легочным бластомикозом незаразны.</span></p>\r\n<p><span><span> </span></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-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Среди внелегочных поражений наиболее часто встречается кожная форма бластомикоза (40–80% случаев). Кожный бластомикоз протекает с везикуло-папулезными или папулезно-пустулезными высыпаниями, которые трансформируются в язвенные дефекты, покрытые обильными грануляциями. Отделяемое из участков изъязвления носит кровянистый или гнойный характер. Язвы могут распространяться на слизистую оболочку ротовой полости, глотки и гортани. Заживление язв происходит с образованием тонкого мягкого рубца. Возможно формирование подкожных абсцессов.</span></p>\r\n<p><span><span> </span></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-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">На долю костной формы приходится 25–50% случаев бластомикоза внелегочной локализации. Протекает преимущественно в виде остеомиелита длинных трубчатых костей, позвоночника, ребер. В зоне поражения нередко образуются абсцессы окружающих мягких тканей, свищевые ходы, артриты близлежащих суставов.</span></p>\r\n<p><span><span> </span></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-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Мочеполовая форма бластомикоза (10–30% случаев) чаще диагностируется у мужчин. Клиническая картина соответствует орхиту, эпидидимиту, простатиту; может отмечаться гематурия и пиурия. Заражение женщин мочеполовым бластомикозом происходит половым путем и встречается редко. При диссеминированном бластомикозе могут поражаться внутренние органы с развитием абсцессов печени, перикардита, надпочечниковой недостаточности и пр. При вовлечении ЦНС возникают абсцессы головного мозга, менингит.</span></p>\r\n<p><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;\"> </span></p>",
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