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1.
J Cardiothorac Surg ; 18(1): 5, 2023 Jan 06.
Artigo em Inglês | MEDLINE | ID: mdl-36609288

RESUMO

BACKGROUND: Pulmonary sequestration is a rare congenital lung anomaly, presenting mostly in childhood and adolescence. CASE PRESENTATION: We report the case of a 26-year-old male patient presenting with pleuritic left sided chest pain and haemoptysis. Computed tomography of the chest showed features of intralobar pulmonary sequestration involving the left lower lobe, with arterial supply arising from the descending thoracic aorta above the diaphragm and normal venous drainage. Video assisted thoracic surgery was planned to perform a left lower lobectomy. Considering the risk of bleeding from the large artery supplying the sequestered segment, a posterolateral thoracotomy incision was made and left lower lobectomy was completed, with successful division of the arterial feeder. The patient was discharged home without complications. Pathologic examination of the specimen grossly revealed partial division of the lobe by two fissures with extensive adhesions into an upper and lower portion with no clear demarcation and a large vessel which enters the lower portion at the posterior inferior aspect, separate from the hilum with a diameter 10 mm. Microscopically, both portions of the lobe showed normally alveolated lung tissue with patchy recent intra-alveolar haemorrhage and evidence of chronic inflammation in the sequestered segment. There was no evidence of malignancy. CONCLUSION: This case highlights the rare presentation of pulmonary sequestration in adulthood and the importance of imaging to identify anomalous arterial supply to the sequestered segment in the left lower lobe of the lung. The use of safe surgical techniques to control the anomalous systemic arterial feeding vessel cannot be overemphasized.


Assuntos
Sequestro Broncopulmonar , Masculino , Adolescente , Humanos , Adulto , Sequestro Broncopulmonar/diagnóstico por imagem , Sequestro Broncopulmonar/cirurgia , Pulmão/diagnóstico por imagem , Pulmão/cirurgia , Pulmão/irrigação sanguínea , Hemoptise/etiologia , Artérias/patologia , Tomografia Computadorizada por Raios X
2.
Indian J Thorac Cardiovasc Surg ; 37(3): 299-302, 2021 May.
Artigo em Inglês | MEDLINE | ID: mdl-33958838

RESUMO

There is a deficit of literature regarding the association between nickel allergy-induced symptoms and implanted devices. This report describes a case of nickel allergy causing debilitating migraine-like symptoms, failing to resolve with medical therapy, requiring surgical removal of the device and repair of the defect.

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