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CHAPTER

41

Fetal Hydrops

Deborah Levine

SUMMARY OF KEY POINTS

• Hydrops is deined as an abnormal accumulation of

interstitial luid in at least two body cavities (pleural,

peritoneal, or pericardial) or one body cavity in association

with anasarca (generalized massive edema).

Placentomegaly and polyhydramnios are common indings

in cases of hydrops but are not needed for the diagnosis.

• Hydrops represents a terminal stage for many conditions,

the vast majority of which are fetal in origin.

• The onset of hydrops signiies fetal decompensation.

• Immune causes can be successfully treated in utero, as

can an increasing number of nonimmune causes.

• Middle cerebral artery Doppler ultrasound can be used to

assess fetuses at risk for anemia.

• A team approach using obstetric imagers, maternal fetal

medicine specialists, neonatologists, and geneticists can

help to decide which cases are suitable for therapeutic

intervention.

CHAPTER OUTLINE

SONOGRAPHIC FEATURES

Ascites

Pleural Effusions

Pericardial Effusions

Subcutaneous Edema

Placentomegaly

Polyhydramnios

ETIOLOGY

IMMUNE HYDROPS

Noninvasive Assessment of

Alloimmunization

NONIMMUNE HYDROPS

Pathophysiology

Causes and Associations

Cardiovascular Abnormalities

Neck Abnormalities

Thoracic Anomalies

Gastrointestinal Anomalies

Urinary Tract Anomalies

Lymphatic Dysplasia

Monochorionic Twins

Chromosomal Anomalies

Tumors

Anemia

Infection

Genetic Disorders

Metabolic Disorders

Skeletal Disorders

Endocrine Disorders

Drugs

Idiopathic Disorders

DIAGNOSTIC APPROACH TO

HYDROPS

History

Complete Obstetric Ultrasound

Maternal Investigations

Fetal Investigations

Performing PUBS

Fetal Transfusion

Cavity Aspiration

Postnatal Investigations

FETAL WELFARE ASSESSMENT IN

NONIMMUNE HYDROPS

OBSTETRIC PROGNOSIS

Maternal Complications (Mirror

Syndrome)

Delivery

Predelivery Aspiration Procedures

Postnatal Outcome

CONCLUSION

Hydrops fetalis is an end-stage process for a number of diferent

diseases. It is deined as an abnormal accumulation of

interstitial luid in at least two body cavities (pleural, peritoneal,

or pericardial) or one body cavity in association with anasarca

(generalized massive edema). Placentomegaly and polyhydramnios

are common indings in cases of hydrops but are not needed for

the diagnosis.

Lymphangiectasia, which is abnormal dilatation of the

lymphatic vessels, should not be mistaken for hydrops. In

the irst trimester, general body wall lymphangiectasia can

have a “space suit” appearance (Fig. 41.1) due to the luid in

the skin and/or subcutaneous tissues. he inding has a poor

prognosis, with 26 in 30 prospectively identiied cases in the

irst trimester having abnormal karyotype. 1 However, because

there is not typically luid in other body cavities, this is

not hydrops.

Hydrops is the late stage of many processes that lead to

redistribution of body luids among the intravascular and

interstitial compartments. his imbalance of luid can have many

causes (Table 41.1). here are at more than 150 diferent causes

of fetal hydrops. Many of the causes and associations with hydrops

overlap. he basic etiology of hydrops is an imbalance of interstitial

luid, which may be caused by myocardial failure, high-output

cardiac failure, decreased colloid oncotic plasma pressure

(anemia), increased capillary permeability, and/or obstruction

of venous and lymphatic low.

1412

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