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EDUCATION EXHIBIT |
Department of Radiology, University of Arkansas for Medical Sciences Little Rock, Arkansas
Obstetric ultrasonography (US) can vary in complexity, depending on the stage of gestation. A complete obstetric US examination performed in the second or third trimester requires the documentation of specific fetal anatomic structures. Discipline and expertise are needed to obtain images that allow the comparison of these landmarks from one examination to another. A comprehensive US survey is reported to be highly accurate for the detection of fetal abnormalities (1,2). The need to define what constitutes a complete obstetric US examination prompted the American College of Radiology and the American Institute of Ultrasound in Medicine to issue practice guidelines. These guidelines can be accessed through the organizational Web sites, at http://www.acr.org (quality and patient safety section) and http://www.aium.org/publications/clinical/obstetrical.pdf. Among the requirements outlined in these guidelines is the documentation of the presence of the fetal extremities. This minimum requirement applies to all second- and third-trimester examinations, regardless of the indication. In most US clinics, common indications for obstetric US include estimation of fetal age, vaginal bleeding, and discrepancy between fetal size and estimated gestational age according to menstrual history. However, when an examination is requested specifically to seek a fetal anomaly, the level of expertise and the requirements of the examination change. Such a request may be precipitated by family history, abnormal results of a serum screening test, or an abnormality seen at a prior US examination. The routine examination is then converted to a targeted obstetric US examination in which a more intensive search for chromosomal markers is performed.
A targeted fetal musculoskeletal US examination begins with the routine demonstration of all four extremities. In skeletal dysplasias manifested by bone shortening, it is mandatory to measure the humerus, femur, tibia, and radius, at a minimum. Measurements of the ulna and fibula may be added as needed to help narrow the diagnosis to the micromelic, rhizomelic, or mesomelic type of skeletal dysplasias. Although measurements of the bones of the fetal hands have been published (3), such measurements are not routinely obtained. Instead, the hands are imaged to look for typical features that may be suggestive of a chromosomal anomaly (47). The search is especially important when other chromosomal markers have been detected in the brain, chest, or abdomen. When diminished fetal motion is suspected, spontaneous movements of the fetal hands also can be assessed (8). In these instances, a thorough knowledge of hand abnormalities is essential. In diagnostic clinics that do not encounter fetal anomalies frequently, there is a tendency to send patients to a tertiary referral center that has more experience in dealing with these cases. When such a referral is not possible or not easily achievable, the radiologist is left with the task of interpreting the US findings and deriving a differential diagnosis. Among the conditions that are strongly associated with hand anomalies, trisomy 18 tops the list (912). Short digits also have been reported in Down syndrome (13,14), as has polydactyly in trisomy 13 (15).
The main objection to performing a detailed evaluation of the fetal hands is that it is too time-and labor-intensive (16). It is true that it takes a certain level of expertise and experience to obtain a clear view of a specific hand abnormality. It could be quite frustrating, trying to capture an image of a very mobile upper extremity, especially in the presence of polyhydramnios, which may be associated with musculoskeletal abnormalities. With the increasing interest in three-dimensional imaging, the fetal extremities have been among the first targets for showing the advantages of three-dimensional over two-dimensional US. Surface rendering algorithms have helped provide exquisitely detailed images of the whole hand and wrist, adding another dimension to the documentation of anomalies (1721).
The article by Rypens, Dubois, Garel, Four-net, Michaud, and Grignon in this issue of RadioGraphics provides a concise summary of fetal hand abnormalities that can be detected with US. Publications that deal with hand abnormalities are definitely in the minority when compared with those about other fetal anomalies, and it is refreshing to see a concise review article on the subject. Rypens and colleagues effectively classify fetal hand anomalies into six groups, thereby providing a framework on which further characterization may be based. Although the sonologist may still need to consult the literature for further details about a specific hand anomaly (2227), this article serves as a good starting point for general reference. The brief treatment of each major category of anomaly is accompanied by excellent figures that reinforce the verbal definition or description of that category and leave a lasting impression in the readers mind. Every radiologist who performs obstetric US can benefit greatly from this review of the US features of hand anomalies that may be observed during routine fetal evaluations.
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