Case Description: A 1-year-old spayed female domestic shorthair cat was evaluated for a sternal defect and ventral abdominal wall hernia.
Clinical Findings: The cat appeared healthy. Palpation revealed a sternal defect, and the heart could be observed beating underneath the skin at the caudoventral aspect of the thorax. A 3-cm-diameter freely movable mass, consistent with a hernia, was also palpated at the cranioventral aspect of the abdomen. Thoracic radiographic and CT images revealed a sternal cleft, cranial midline abdominal wall hernia, and peritoneopericardial diaphragmatic hernia (PPDH).
Treatment And Outcome: Thoracotomy and celiotomy were performed. The sternal cleft was repaired with a porcine small intestinal submucosa graft, titanium contourable mesh plate, and interrupted 25-gauge cerclage wires. A diaphragmatic herniorrhaphy was used to correct the PPDH. Thoracic radiographs were obtained immediately after surgery to confirm repair of the sternal cleft, abdominal wall hernia, and PPDH and at 1 and 3 months after surgery to assess the surgical implants, which had not migrated and were intact with only mild bending at the cranial and caudal margins of the mesh plate. At both recheck examinations, the cat appeared healthy with no complications reported by the owner.
Clinical Relevance: A novel surgical technique was used to successfully repair a large sternal cleft in an adult cat with no postoperative complications reported. This technique may be useful for the treatment of sternal clefts in other cats. This was the first report to describe an adult cat with congenital defects consistent with incomplete pentalogy of Cantrell.
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http://dx.doi.org/10.2460/javma.254.9.1099 | DOI Listing |
Cardiol Young
October 2024
Department of Pediatrics, Institute for Health Sciences Education, Georgetown Public Hospital Corporation, Georgetown, Guyana.
Cureus
August 2024
Internal Medicine, I.K. Akhunbaev Kyrgyz State Medical Academy, Bishkek, KGZ.
The sternal cleft (SC) is a rare congenital anomaly characterized by a complete or partial separation of the sternum, leading to significant clinical concerns, including respiratory and cardiac instability. Due to its rarity, the SC often poses surgical challenges. This case report highlights the management of two neonates with SCs, emphasizing the critical role of early multidisciplinary intervention.
View Article and Find Full Text PDFTurk Gogus Kalp Damar Cerrahisi Derg
April 2024
Department of Surgery, King Abdulaziz University Hospital, King Abdulaziz University, Jeddah, Saudi Arabia.
Turk Gogus Kalp Damar Cerrahisi Derg
April 2024
Department of Cardiovascular Surgery, Biruni University Faculty of Medicine, İstanbul, Türkiye.
Failed midline ventral fusion of sternal bars is the cause of complete sternal cleft, which is a rare congenital anomaly that may cause cardiopulmonary compromise. Very few cases of complete sternal cleft have been reported so far in the literature. Surgical correction is recommended to protect mediastinal structures and to restore respiratory dynamics.
View Article and Find Full Text PDFTurk Gogus Kalp Damar Cerrahisi Derg
April 2024
Department of Thoracic Surgery, Biruni University Faculty of Medicine, Istanbul, Türkiye.
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