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Official Proceedings - AIUM

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American Institute of Ultrasound in Medicine <strong>Proceedings</strong> J Ultrasound Med 32(suppl):S1–S134, 20131536801 Cloacal Exstrophy: When an Omphalocele Is Not Just anOmphaloceleReza Pakdaman, 1 * Anne Kennedy, 1,2 Mark Molitor, 3 JaniceByrne, 2 Paula Woodward 1,2 1 Radiology, 2 Obstetrics and Gynecology,3 Surgery, University of Utah, Salt Lake City, Utah USAObjectives—(1) Illustrate additional congenital abnormalitiesthat, when seen in a fetus with an omphalocele, should lead to the diagnosisof cloacal exstrophy. (2) Illustrate the role of fetal magnetic resonanceimaging (MRI) in making the diagnosis. (3) Correlate prenatalfindings with postnatal imaging and surgical findings in survivors. (4) Illustrateautopsy findings.Methods—Retrospective review of 7 cases seen at 1 institution.Prenatal findings were correlated with postnatal multimodality imaging,surgical, or autopsy results.Results—7 cases were seen for prenatal ultrasound (US). FetalMRI was performed in 4. See Table 1 for US findings. Pregnancy outcomeswere live birth in 4, perinatal death in 1, intrauterine demise in 1,and termination of pregnancy in 1.Conclusions—The presence of an omphalocele should alert thesonologist to perform additional views and seek other anomalies in an effortto refine the diagnosis. In particular, inability to demonstrate a normalbladder and rectum and the presence of spine abnormalities shouldheighten suspicion for cloacal exstrophy. Cloacal exstrophy is a rare anomalynot associated with aneuploidy; however, the condition requires multiplesurgeries, and survivors require lifelong specialist care. Faced with thelong-term consequences of this condition, families may choose terminationof pregnancy. Therefore, correct prenatal diagnosis is of paramountimportance. In ongoing pregnancies, delivery should be planned at an appropriatefacility with the resources to manage children with complexmetabolic, surgical, and psychosocial needs.Table 1. US FindingsCase AWD Bladder Anus Spine Genitalia1 Y N NA Ab NA2 Y N N Ab Amb3 Y N N Ab Amb4 Y N NA NA Bifid5 Y N NA Ab Amb6 Y N NA Ab NA7 Y N NA Ab NAAb indicates abnormal; Amb, ambiguous; and AWD, abdominal wall defect.1536808 Imaging Spectrum of Fetal Autosomal Recessive PolycysticKidney DiseaseTony Trinh, 1 * Anne Kennedy, 2,3 Joe Sherbotie, 4 Janice Byrne 31School of Medicine, 2 Radiology, 3 Obstetrics and Gynecology,4Nephrology, University of Utah, Salt Lake City, Utah USAObjectives—(1) Illustrate the spectrum of findings of fetal autosomalrecessive polycystic kidney disease (ARPKD). (2) Correlate fetalstudies with postnatal imaging or autopsy results.Methods—Retrospective review of cases seen at a single referralcenter.Results—Renal enlargement was our most consistent finding.Most kidneys looked normal up to 20 weeks but abnormally echogenickidneys were seen as early as 16 weeks. Echogenicity varied from theclassic highly echogenic pattern with loss of normal architecture to increasedechogenicity with identifiable medullary pyramids to a pattern ofvery echogenic pyramids similar to that seen in medullary sponge kidneyin adults. Amniotic fluid volume was variable from severe oligohydramniosto normal. Not all cases had evidence of pulmonary hypoplasia.Conclusions—Not all cases of ARPKD present with the classicfindings of large, brightly echogenic kidneys and severe oligohydramnios.This reflects the variable phenotype with perinatal, neonatal,and infantile types described. It is very important that sonologists recognizethe full spectrum of findings to suggest ARPKD and differentiate itfrom other causes of renal enlargement or abnormal renal echogenicity.Fetuses with echogenic kidneys require postnatal follow-up. The prognosisis variable. Awareness of the possibility of ARPKD will result in appropriatetesting of the parents for recessive gene carrier status. Affectedcouples will have a 1:4 recurrence risk for future pregnancies.1536912 Abnormal Ultrasound Findings in Patients With ClinicalSuspicion of Chronic Liver Disease in Sokoto and ItsEnvironsSadisu Maaji,* Abdulmuminu Yakubu, Danielle OdunkoRadiology, Usmanu Danfodiyo University Teaching Hospital,Sokoto, Nigeria; Radiology, Federal Medical Center BirninKebbi, Birnin Kebbi, NigeriaObjectives—To describe the pattern of abnormal ultrasonographicfindings in patients with clinical suspicion of chronic liver diseasein Nigeria, especially from the northwestern region.Methods—A total of 61 consecutive patients with clinical signsand symptoms of chronic liver disease attending medical outpatient clinicsat the Department of Medicine, Usmanu Danfodiyo University TeachingHospital, and Federal Medical Center Birnin Kebbi were scanned atradiology departments for any abnormal intra- abdominal findings fromMay 2011 to April 2012. The exclusion criteria were patients with confirmedliver biopsy or diagnosis of chronic liver disease. Patients with cardiaccirrhosis and tropical splenomegaly syndrome were also excluded inthis study.Results—A total of 61 abdominal ultrasound examinationswere performed during this study period. All the cases met the inclusioncriteria. The mean age was 46 ± 12.6 years (range, 50 years). The meanliver sizes were 13.25 ± 1.48 cm (range, 11 cm) and 14.00 ± 0.77 cm(range, 0.77 cm) for right and left lobes, respectively. The mean spleensize was 15.9 ± 1.22 cm (range, 6 cm). The sex distribution was 43 males(70.49%) and 18 females (29.5%). Of the 61 cases included, the indicationsfor abdominal ultrasound were hepatitis in 1 (1.61%), liver cirrhosisin 20 (50.82%), obstructive jaundice in 2 (3.28%), chronic liver disease in25 (40.98%), and chronic abdominal swelling in 2 (3.2%). Gallbladderwall thickening was demonstrated in 49 (80.33%) of the patients, while 12(19.67) showed a normal gallbladder wall. Ascites was demonstrated in 45(73.77%) of the patients, and the remaining 16 (26.23%) of the patientshad no ascites. Destroyed intrahepatic vascular architecture was demonstratedin 58 (95%), while 3 (4.9%) showed normal vascular architecture.Conclusions—Ultrasound is useful in the diagnosis of chronicliver disease in daily clinical practice. However, the sensitivity can be improvedif a high-frequency probe is used and done by experienced anddedicated operators. Liver biopsy remains the gold standard, especiallywhen patients are clinically asymptomatic.1536944 Carotid Ultrasound May Not Be Sufficient to PerformCarotid EndarterectomyRobert Colvin, 1 * Alvaro Magalhaes 2 1 Kansas City Universityof Medicine and Biosciences, Kansas City, Missouri USA;2Radiology, University of Missouri, Kansas City, Missouri USAObjectives—Evaluate the accuracy of ultrasound to determinetreatment of carotid artery stenosis when compared to advanced imagingmodalities.Methods—This study consisted of 47 patients who underwentimaging for carotid artery stenosis by magnetic resonance imaging withangiography or computed tomography with angiography at a Midwest regionalmedical center over a 27-month period. The results of the previouslyobtained duplex ultrasound studies were compared to results fromadvanced imaging studies.S93

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