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Sternal Development and Variations and Anomalies in Patients With Microtia: Evaluation Using 3-Dimensional Computed
MeiRong Yang1, Haiyue Jiang, Xiaobo Yu
1From the Departments of *Auricular Reconstruction and †Radiology, Plastic Surgery Hospital, Peking Union Medical College, Beijing, China.
Journal of Computer Assisted Tomography
|March 16, 2017
Summary
This study examined sternal development and anomalies in microtia patients, finding wide variations and a lower incidence of sternal foramina. Congenital sternal anomalies interact with microtia, highlighting developmental complexities.
Area of Science:
- Anatomy
- Medical Imaging
- Genetics
Background:
- Microtia is a congenital ear anomaly.
- Sternal development involves complex ossification and fusion processes.
- Congenital sternal anomalies can occur independently or as part of syndromes.
Purpose of the Study:
- To evaluate sternal development and variations in microtia patients.
- To determine the incidence of congenital sternal anomalies in this population.
- To investigate potential interactions between microtia and sternal anomalies.
Main Methods:
- Retrospective analysis of 212 patients with microtia.
- Preoperative 3D chest CT scans were utilized.
- Statistical analyses included ANOVA, Spearman, chi-square, and Fisher's exact tests.
Main Results:
- Significant individual variations in sternal components (manubrium, body, xiphoid) were observed.
- Sternal foramina were found in 2.8% of patients, all in the inferior body.
- Sternal clefts occurred in 1.9%, with two cases associated with a distal foramen.
Conclusions:
- Sternal development exhibits considerable variation in microtia patients.
- A distinct distribution of mesosternal types was noted across the age range.
- The incidence of sternal foramina appears lower in patients with microtia.
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