01.10.2020 Views

ultrasound diagnosis of fatal anomalies

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

THORAX

Fig. 4.15 Left-sided diaphragmatic hernia. The

same case viewed longitudinally. The diaphragm is

seen ventrally but not dorsally. The intestine is seen

continuously up into the thorax.

1

2

3

4

5

Prognosis: The prognosis depends on the severity

of respiratory distress, especially hypoplasia

of the lung and other concomitant anomalies.

The earlier the diagnosis is made in prenatal

screening, the poorer the prognosis (15–50%

mortality). The prognosis worsens if the diagnosis

is made prior to 24 weeks’ gestation and hydramnios

develops. Mortality is influenced by

the neonatologist’s experience and possibly also

concurrent the use of extracorporeal membrane

oxygenation (ECMO). The value of intrauterine

prognostic factors for determining the extent of

hypoplasia of the lungs (area of the lung, Doppler

sonography of the pulmonary artery, and

amniotic flow in the trachea) is uncertain. Intrauterine

fetal surgery (e.g., tracheal blockage)

is still in the experimental phase. Neonates who

can be stabilized postnatally prior to surgery

have about a 65–85% chance of survival. Some

children develop a chronic respiratory distress

syndrome.

Self-Help Organization

Title: CHERUBS Association for Congenital Diaphragmatic

Hernia Research, Advocacy, and

Support

Description: Support and information to

families of children born with congenital diaphragmatic

hernias. Phone support, online

services, on-call volunteers, state and country

representatives, pen pals, medical research,

information and referrals, newsletter.

Scope: International network

Founded: 1995

Address: P.O. Box1150, Creedmoor, NC 27565,

United States

Telephone: 1–888–834–8158 or 919–693–

8158

Fax: 707–924–1114

E-mail: info @cherubs-cdh.org

Web: http://www.cherubs-cdh.org

References

Adzick NS, Vacanti JP, Lillehei CW, O’Rourke PP, Crone

RK, Wilson JM. Fetal diaphragmatic hernia: ultrasound

diagnosis and clinical outcome in 38 cases. J

Pediatr Surg 1989; 24: 654–7.

Albanese CT, Lopoo J, Goldstein RB, et al. Fetal liver position

and perinatal outcome for congenital diaphragmatic

hernia. Prenat Diagn 1998; 18: 1138–42.

Al-Shanafey S, Giacomantonio M, Henteleff H. Congenital

diaphragmatic hernia: experience without extracorporeal

membrane oxygenation. Pediatr Surg Int

2002; 18: 28–31.

Kalache KD, Chaoui R, Hartung J, Wernecke KD,

Bollmann R. Doppler assessment of tracheal fluid

flow during fetal breathing movements in cases of

congenital diaphragmatic hernia. Ultrasound Obstet

Gynecol 1998; 12: 27–32.

Kasales CJ, Coulson CC, Meilstrup JW, Ambrose A, Botti

JJ, Holley GP. Diagnosis and differentiation of congenital

diaphragmatic hernia from other noncardiac

thoracic fetal masses. Am J Perinatol 1998; 15: 623–

8.

Lewis DA, Reickert C, Bowerman R, Hirschl RB. Prenatal

ultrasonography frequently fails to diagnose congenital

diaphragmatic hernia. J Pediatr Surg 1997;

32: 352–6.

78

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!