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Желудочно-кишечные

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  1. ДРУГИЕ ЗАБОЛЕВАНИЯ, ВЫЗЫВАЮЩИЕ ОСТРЫЕ ЖЕЛУДОЧНО-КИШЕЧНЫЕ КРОВОТЕЧЕНИЯ
  2. Желудочно-кишечные заболевания
  3. Желудочно-кишечные кровотечения
  4. Желудочно-кишечные кровотечения
  5. Некоторые желудочно-кишечные гормоны
  6. ОСТРЫЕ ЖЕЛУДОЧНО-КИШЕЧНЫЕ КРОВОТЕЧЕНИЯ ОПУХОЛЕВОЙ ЭТИОЛОГИИ

Инфаркт или резекция кишки (ниже двенадцатиперстной кишки), селезёнки, печени или жёлчного пузыря, когда-либо, по любым причинам (счёт 2, если более, чем в одном месте) Мезентериальная недостаточность Хронический перитонит

Стриктуры или хирургические операции на верхней части ЖКТ, когда-либо

Мышечно-скелетные Мышечная атрофия или слабость

Деформирующий или арозивный артрит (включая вправимые деформации, исключая аваскулярные некрозы) Остеопороз с переломами или коллапсом позвонков (исключая аваскулярный некроз) Аваскуляриый некроз (счёт 2, если >1) Остеомиелит

Кожные

Рубцующаяся хроническая алопеция Обширное рубцевание или панникулит (кроме скальпа и подушечек пальцев)


1(2)

1(2)

1(2)

1(2)


160 ♦ Ревматология ♦ Системная красная волчанка

Окончание табл. 3

 

   
Изъязвление кожи (исключая тромбоз) в течение более 6 мес Преждевременная недостаточность гонад Сахарныйдиабет (вне зависимости от терапии) Малигнизация(исключая дисплазию) (счёт 2, если более одной локализации) 1 1 1 1(2)

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СИСТЕМНАЯ СКЛЕРОДЕРМИЯ


Системная склеродермия — аутоиммун­ное заболевание соединительной ткани, основные клинические признаки которо­го обусловлены распространёнными на­рушениями микроциркуляции, фибро­зом кожи и внутренних органов. Системная склеродермия — важнейший представитель склеродермической груп­пы болезней, к которым также относят­ся ограниченная (очаговая)склеродер­мия, диффузный эозинофильный фасци-ит, склередема Бушке, мультифокаль-ный фиброз, индуцированные формы склеродермии и псевдосклеродермичес-кие синдромы.

МКБ-10: М34 Системный склероз; М34.0 Прогрессирующий системный склероз; М34.1 Синдром CREST; M34.2 Системный склероз, вызванный лекар­ственными средствами и химическими соединениями; М34. 8 Другие формы си­стемного склероза.

Аббревиатуры: ССД — системная скле­родермия; ИЗЛ — интерстициальное заболевание лёгких.

ЭПИДЕМИОЛОГИЯ11

• Распространённость ССД различает­
ся между отдельными географически­
ми зонами и этническими группами, в
том числе проживающими в одном ре­
гионе.

• Первичная заболеваемость колеблет­
ся от 3,7 до 19,0 на 1 млн населения
в год.

• ССД чаще встречается у женщин (со­
отношение 5—7 к 1) в возрасте 30—
60 лет.

Профилактика не проводится. Скрининг не проводится.


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