Hydrops fetalis

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Classification according to ICD-10
P56 Hydrops fetalis due to hemolytic disease
P83.2 Hydrops fetalis, not due to hemolytic disease
ICD-10 online (WHO version 2019)

As hydrops fetalis (Syn. Hydrops congenitus universalis ) in which is prenatal diagnosis a generalized fluid accumulation designated extending over large parts of the body of an unborn child has spread and in serous body cavities ( pleural , peritoneal cavity , pericardium is) as well as in the soft tissues. In the ultrasound , a pronounced edema is particularly visible, through which the child's skin is clearly lifted from the body.

A distinction is made between hydrops fetalis with and without isoimmunization (immunological and nonimmunological hydrops fetalis).

The presence of hydrops fetalis is considered a sonographic soft marker , which is an indication of a chromosome peculiarity , an organic malformation or a disease in the child.

It occurs more than average in:

See also

Hemolytic disease of the newborn - nuchal translucency - hygroma colli - Dorsonuchales edema - hygroma dura mater - hygroma praepatellare - Hygromatosis

Web links

Individual evidence

  1. Peter Reuter: Springer Lexicon Medicine. Springer, Berlin a. a. 2004, ISBN 3-540-20412-1 , p. 961.