Prenatal diagnosis and natural history of the fetus with a congenital diaphragmatic hernia: initial clinical experience.

To study the accuracy of prenatal diagnosis and define the natural history of fetal congenital diaphragmatic hernia (CDH), we reviewed experience with CDH at The University of California, San Francisco (UCSF) over the last three years. All nine babies born in our institution (inborns) and six of 11 babies referred from other hospitals after birth (outborns) died, an overall mortality of 75%. All had pulmonary hypoplasia.

Amnionicity and chorionicity in twin pregnancies: prediction using ultrasound.

A total of 66 twin pregnancies was studied antenatally with ultrasound, followed up clinically, and the placentae examined pathologically to determine if, solely on the basis of antenatal sonography, an accurate assessment of amnionicity and chorionicity could be made. Sonographic features noted included number of placental sites, whether a membrane separating the fetuses could be visualized, fetal position and amount of amniotic fluid, and in some cases fetal positioning vis-a-vis each other and the uterine wall. Documentation of two placental sites confirms the presence of a dichorionic and, therefore, a diamniotic pregnancy.

The distal femoral epiphyseal ossification center in the assessment of third-trimester menstrual age: sonographic identification and measurement.

The distal femoral epiphyseal secondary ossification center (DFE), which can be reliably identified and measured sonographically, may assist the sonologist in predicting third-trimester menstrual age. Between 28 and 35 menstrual weeks, the percentage of fetuses with a DFE progressively increases. Although the mean age at DFE appearance is approximately 32-33 menstrual weeks, the DFE may be seen as early as 29 menstrual weeks.

Obstetrical magnetic resonance imaging: fetal anatomy.

Nine patients who were 34-36 weeks pregnant underwent magnetic resonance (MR) imaging. Sagittal images using spin echo technique (TR 2.0 sec, TE 28 msec) were optimal for delineating fetal anatomy.

Obstetrical magnetic resonance imaging: maternal anatomy.

Eleven patients whose pregnancies were at 34-36 weeks of gestational development underwent magnetic resonance (MR) imaging. Images of the maternal pelvis were assessed for anatomical changes of pregnancy in comparison with MR images of five non-pregnant volunteers. The relationship of the fetal presenting part to the internal os of the cervix was seen in all patients.

Minimal fetal renal pyelectasis.

To assess the possible relationship between the degree of maternal hydration and the sonographic identification of minimal fetal renal pyelectasis, a prospective study was performed in which fetuses demonstrating mild dilation of the renal pelvis (maximum diameter ranging from 3 to 11 mm) were reexamined after the mothers refrained from oral intake for 12 hours. Complete or almost complete resolution of the pyelectasis occurred in only four of 17 kidneys (23.5 per cent) while the remaining fetal kidneys demonstrated little or no change in the degree of pyelectasis following maternal dehydration.

Comparison of magnetic resonance imaging and ultrasonography in the evaluation of abdominal aortic aneurysms.

Magnetic resonance imaging (MRI) was used to evaluate abdominal aortic aneurysms in 27 patients. The findings were compared retrospectively with CT, ultrasound (US), and angiography in 17 cases and prospectively with US in 10 cases. MRI identified the renal arteries in all cases, demonstrated involvement at or above the origin of the renal arteries in eight patients, and showed extension of the aneurysm into the iliac arteries in 12 cases.

Investigation of nonimmune hydrops fetalis.

Fifty pregnancies complicated by fetal ascites and generalized edema are reviewed and their prenatal findings, obstetric management, and fetal outcome are discussed. From the myriad of maternal, fetal, and placental problems which are known to cause nonimmune hydrops fetalis, many different causes of the disorder could be identified in 84% of all patients studied by extensive prenatal and postnatal workup. Therefore, in only 16% of the cases was the nonimmune hydrops fetalis labeled "idiopathic.

The fetal cisterna magna.

Antenatal sonography routinely images the fetal cisterna magna. The identification of a prominent cisterna magna on a routine antenatal sonogram performed for obstetric indications may raise the question of a congenital posterior fossa lesion. To delineate the size of the fetal cisterna magna, standardized measurements for the midsagittal depth of the cisterna magna were prospectively obtained on 219 consecutive antenatal sonograms in fetuses of 15 menstrual weeks or more.

Ultrasound evaluation of benign sciatic nerve sheath tumors.

The ultrasonograms of three patients with surgically proven benign tumors of the sciatic nerve sheath were reviewed. Two lesions were neurilemmomas and one was a neurofibroma. All lesions appeared hypoechoic and often demonstrated characteristics typically associated with cystic abnormalities.

High-resolution sonographic assessment of the fetal extremities.

Recent advances in ultrasound technology, especially phased-array sonography, now permit striking visualization of fetal morphology. Although several reports document the sonographic appearance of the fetal appendicular skeleton, no reports describe the nonosseous structures of the fetal limbs. Prior to the middle of the second trimester of pregnancy, adequate size and intrinsic subject contrast enable distinction among numerous limb structures.

Ultrasonographic determination of qualitative amniotic fluid volume in intrauterine growth retardation: reassessment of the 1 cm rule.

To assess the relative diagnostic efficacy of the "1 cm sign" for qualitative amniotic fluid volume determination in the prenatal evaluation of intrauterine growth retardation, 125 pregnancies resulting in small-for-gestational age infants were studied in a retrospective fashion. Qualitative amniotic fluid volume was designated as normal if at least one pocket of amniotic fluid measuring 1 cm in broadest diameter was identified. Of the 125 pregnancies with delivery of small-for-gestational age infants, only five would have been correctly predicted prenatally with qualitative amniotic fluid volume used as the sole criterion for intrauterine growth retardation.

Management of the fetus with an abdominal wall defect.

Eleven fetuses with omphalocele and two with gastroschisis were diagnosed by prenatal ultrasonographic examination. Intact omphalocele was accurately distinguished from gastroschisis by detection of a membranous sac covering the herniated viscera, by liver protruding from the abdomen, and by the frequent association of major structural anomalies. Gastroschisis was characterized by the absence of these findings and the presence of bowel loops floating freely in the amniotic fluid.

Management of ventriculomegaly in the fetus.

We studied 24 human fetuses with cerebral ventriculomegaly by serial obstetric ultrasound to define the natural history of fetal ventricular enlargement and to develop a management strategy. In 10 fetuses, ventriculomegaly was associated with other severe anomalies; nine of these families chose to terminate the pregnancy. In three other severely affected fetuses in whom ventriculomegaly was detected serendipitously late in gestation, routine obstetrical management was performed; none survived.

Fetal renal dysplasia: sonographic evaluation.

In an attempt to predict histologic fetal renal dysplasia among fetuses with obstructive uropathy, three antenatal sonographic features (presence of renal cortical cysts, echogenicity of renal parenchyma, and degree of hydronephrosis) were studied. Identification of renal cortical cysts in the kidneys of fetuses with obstructive uropathy enabled accurate prediction of renal dysplasia. Of 49 fetal kidneys with obstructive uropathy, all 15 kidneys with sonographically visible cortical cysts had severe but not necessarily lethal dysplasia (accuracy of positive prediction = 100%).

Severe nonimmune hydrops fetalis: sonographic evaluation.

Reported survival rates in nonimmune hydrops fetalis vary considerably. Among 27 fetuses exhibiting severe sonographic features of nonimmune hydrops fetalis, 33% survived the neonatal period. For five of the nine survivors, the prognosis remains uncertain or poor.

Prenatal diagnosis of asphyxiating thoracic dysplasia.

A fetus at risk for asphyxiating thoracic dysplasia was studied with ultrasound examination at 16, 18, and 23 weeks of pregnancy. Definite shortness of fetal femora was observed. Radiographic and histologic examinations after pregnancy termination confirmed the diagnosis.

Benign breast lesions: ultrasound detection and diagnosis.

Experience with 2500 patients over age 30 studied by physical examination, x-ray mammography, and sonography enabled definition of several specific clinical situations in which sonography adds meaningful diagnostic information not provided by either of the other examinations. These include: palpable breast masses for cyst-solid differentiation; nonpalpable mammographic masses for cyst-solid differentiation; and women with a symptomatic area in the breast that shows only uniformly dense fibro-glandular tissue on x-ray mammograms. For women with radiographically dense breasts who have no breast symptoms, abnormal physical findings, or mammographic lesions, sonography will identify many benign cysts and also some benign solid lesions, but at best only rarely (none of the 587 cases in this study) will it detect an otherwise occult breast cancer.

Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.

Modern ultrasound imaging devices have increasingly allowed sophisticated prenatal diagnoses of fetal disorders. Embryopathologic and ultrasound findings are reported in five cases of alobar holoprosencephaly that were diagnosed prenatally, two cases as early as 23 menstrual weeks. Specific sonographic findings included a large central cranial fluid collection (a monoventricular cavity lacking ventricular horns and midline structures), a fused thalamus at the floor of this cavity, and characteristic facial features (proboscis, single orbit, single nostril, or severe hypotelorism).

[Role of echography in the diagnosis of extra-uterine pregnancy. Value of the double sac sign].

Ultrasound images showing normal intrauterine pregnancy with embryo practically excludes the presence of an extrauterine pregnancy (E.U.P.