5. 超音波影像發現
CCAM volume = length x width x height of the lesion x 0.52
Fetal CVR = CCAM volume / head circumference
this case = (5.05 x 4.45 x 4.20) x 0.52 / 21.54 = 2.28
9. Congenital Cystic
Adenomatoid Malformation
Definition
A pulmonary anomaly characterized by
overgrowth of terminal bronchioles.
Usually unilateral with variable size
and rate of growth giving rise to clinical
presentations, ranging from
intrauterine fetal demise with hydrops
to discovery in childhood after
recurrent pulmonary infections.
10. Type I , 50%Type II, 40%
Type III,
10%
Congenital Cystic
Adenomatoid Malformation
Cyst < 10mm Cyst in 2-7 cm
Larger in number Few in number (1-4)
Hydrops,
Pulmonary hypoplasia
Favorable prognosis
11. CAM Volume Ration
CVR< 1.6 = favorable prognosis
The average gestational age at the CCAM
growth is reached is 26weeks.
Hydrops?
Placental swelling?
Doppler finding?
CCAM volume = length x width x height of the lesion x 0.52
Fetal CVR = CCAM volume / head circumference
12. Associated anomalies:
The condition is usually isolated.
Unlike diaphragmatic hernia there is no association with
chromosomal defects.
In about 10% of cases there are additional malformations :
· renal abnormalities (bilateral renal agenesis)
· abdominal wall abnormalities
· central nervous system defects (hydrocephalus)
· spinal deformities (cervical spine/thoracic spine)
· gastrointestinal defects
(diaphragmatic hernia, jejunal atresia, tracheoesophageal fistula)
· cardiac anomalies and anomalies of the great vessels
(ventricular septal defect, tetralogy of Fallot, truncus arteriosus)
· sirenomelia (including agenesis of ureters, bladder, urethra, uterus, cervix,
vagina, gallbladder, descending colon, sigmoid colon and rectum, and imperforate
anus)