Extralobar Supradiaphragmatic Pulmonary Sequestration Arising from the Retroperitoneum Through a Congenital Diaphragmatic Defect

Lee, Soojin; Cho, Jeong Su; Hoseok, I; Ahn, Hyo Yeong; Kim, Yeong‐Dae

doi:10.5090/jcs.20.065

Cited by 2 publications

(2 citation statements)

References 7 publications

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“…Combined with imaging and intraoperative findings, the abnormal arteries of nine patients (69.23%) in this study originated from the branches of the descending thoracic aorta, which was slightly lower than the proportion reported in the literature. Some patients with pulmonary sequestration have chest complications such as funnel chest and diaphragmatic hernia 14–16 . In this study, one child with pulmonary sequestration had pectus excavatum.…”

Section: Discussionmentioning

confidence: 59%

“…Some patients with pulmonary sequestration have chest complications such as funnel chest and diaphragmatic hernia. [14][15][16] In this study, one child with pulmonary sequestration had pectus excavatum. After a comprehensive evaluation, a thoracoscopic Nuss surgery was performed simultaneously, which was consistent with the literature report.…”

Section: Discussionmentioning

confidence: 71%

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Imaging and pathological characteristics, treatment, and prognosis of pulmonary sequestration—A retrospective study of 13 cases

Liu

Zhu

et al. 2023

Clinical Respiratory J

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ObjectiveThis study aimed to summarize and analyze the characteristics of pulmonary sequestration to improve our understanding of this disease.MethodsBetween January 2019 and April 2023, the clinical data of 13 patients with pulmonary sequestration underwent surgical treatment at the First Affiliated Hospital of Gannan Medical University.ResultsThe male‐to‐female ratio was 4:9, the age was 0.5 to 60 years, and the average age was 38 ± 19 years. There were 10 and 3 cases of intralobar and extralobar pulmonary sequestration, respectively. Chest enhanced computed tomography (CT) and three‐dimensional vascular reconstruction showed that the abnormal blood vessels were derived from the descending thoracic aorta in nine cases and from other blood vessels in four cases. Three patients underwent thoracoscopic lobectomy, two underwent thoracoscopic segmentectomy, and eight underwent thoracoscopic wedge resection. All the patients successfully completed the surgery and were discharged postoperatively.ConclusionsSome patients with pulmonary sequestration exhibit no obvious symptoms. Patients with clinical symptoms are easily confused for pneumonia, bronchial cysts, lung abscesses, and lung tumors; therefore, patients with pulmonary sequestration are prone to missed diagnosis and misdiagnosis. Currently, enhanced chest CT combined with three‐dimensional vascular reconstruction can accurately show the course, branches, and relationship with the mass of the feeding artery. Routine pathological examination is helpful to further clarify the diagnosis of pulmonary sequestration. Minimally invasive thoracoscopic surgery is the preferred treatment for patients with pulmonary sequestration. Surgical resection is safe and feasible, and satisfactory results are typically obtained.

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Section: Discussionmentioning

confidence: 59%

Section: Discussionmentioning

confidence: 71%

Imaging and pathological characteristics, treatment, and prognosis of pulmonary sequestration—A retrospective study of 13 cases

Liu

Zhu

et al. 2023

Clinical Respiratory J

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Congenital diaphragmatic hernia with associated broncho-pulmonary sequestration: A report of two cases and a literature review

Alhamad,

Anand

2024

NPM

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BACKGROUND: Congenital Diaphragmatic Hernia (CDH) is a severe congenital anomaly with significant morbidity and mortality. It can be isolated or can be associated with other congenital anomalies, including broncho-pulmonary sequestration (BPS). The association of CDH with BPS (CDH+BPS) is uncommon but has been previously reported, and it can complicate the course of the disease in patients with CDH. We report two cases of CDH+BPS that were recently treated at our CDH-Qatar (CDH-Q) program. METHODS: We reviewed CDH-Q program registry to search for CDH+BPS and extracted the data for the identified cases. We also reviewed the previously published literature available on PubMed for similar cases. RESULTS: Out of 53 cases of CDH referred to CDH-Q from January 2018 to December 2022, two cases of CDH+BPS were identified, with an estimated prevalence of 3.8% of this association in our CDH population. Both cases were born at term. Case 1 was diagnosed with CDH+BPS postnatally, while case 2 was diagnosed with CDH antenatally but BPS was diagnosed after birth. Both cases underwent a surgical repair of the CDH with resection of the associated BPS, and the histopathology of the resected lung tissue confirmed the presence of BPS in both. Both cases survived to discharge. CONCLUSION: The association of CDH+BPS is uncommon; however, it can have significant consequences on the management and the prognosis of patients with CDH. Reporting these cases is important to provide a better understanding of this association and its impact on CDH patients.

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Extralobar Supradiaphragmatic Pulmonary Sequestration Arising from the Retroperitoneum Through a Congenital Diaphragmatic Defect

Cited by 2 publications

References 7 publications

Imaging and pathological characteristics, treatment, and prognosis of pulmonary sequestration—A retrospective study of 13 cases

Imaging and pathological characteristics, treatment, and prognosis of pulmonary sequestration—A retrospective study of 13 cases

Congenital diaphragmatic hernia with associated broncho-pulmonary sequestration: A report of two cases and a literature review

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