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bronchopulmonary sequestration/fièvre
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Surgical treatment of infected intralobar pulmonary sequestration: a collective review of patients older than 50 years reported in the literature.
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We report on the rare and surgical treatment of a senile patient of infected intralobar pulmonary sequestration. A 56-year-old male who had complained of headache, vomiting, cough, sputum production, and high fever was admitted to our hospital. Chest computed tomography (CT) showed an infected
Pulmonary sequestration-differences in diagnosis and treatment in a single institution.
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BACKGROUND
Pulmonary sequestration (PS) is a rare congenital lung malformation. In this study, we evaluated the diagnosis and treatment of PS in 31 adult patients at a single institution.
METHODS
A retrospective review of all patients 16 years of age and older with PS in a single institution between
[Pulmonary sequestration associated with localized cystic bronchiectasis and funnel chest].
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A 37-year-old woman, who presented with low grade fever and productive cough, was admitted for evaluation of an abnormal shadow on chest X-ray film. On physical examination, she had bilateral hallux valgus and funnel chest, the center of which was at the fifth rib on the right edge of the sternum.
[Intra-abdominal pulmonary sequestration in an adult: report of an operated case and review of the literature].
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A 39-year-old man presenting fever and abdominal pain for three days was operated. He had similar but less severe complaint three weeks before. On admission, his temperature was around 38 degrees C and the abdomen was slightly tender in the left upper quadrant. His blood count showed 24,600 white
Endostapling the aberrant artery filled with embolized coils for intralobar pulmonary sequestration: a report of two cases.
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Intrapulmonary sequestration is a rare congenital bronchopulmonary malformation. Surgery is generally standard treatment, and thoracoscopic resection has been accepted recently. Some patients have inflammatory change of the sequestrated lung and adhesion to the adjacent organs. In those cases, it is
Pulmonary sequestration in adult patients: a retrospective study.
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OBJECTIVE
Pulmonary sequestration (PS) is a rare congenital malformation. This study presents the characteristics of PS in adult patients, including pulmonary function and concurrent infection, which have not been well documented previously.
METHODS
Patients ≥16 years old with a discharge diagnosis
Neonatal pulmonary sequestration (PS) with rhabdomyomas-like hyperplasia: A case report
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Introduction: Pulmonary sequestration (PS) is a rare pulmonary congenital malformation characterized by disconnection with the tracheobronchial tree or the pulmonary arterial blood supply thus impeding the connection to the arterial blood
Video-Assisted Thoracoscopic Surgery for Pulmonary Sequestrations: Series of 35 Consecutive Patients in a Single Center.
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OBJECTIVE
The aim of this report is to summarize the experience of completely video-assisted thoracoscopic surgery (VATS) for pulmonary sequestration in a single center and to evaluate the long-term outcome in a larger series of patients.
METHODS
The data of 35 pulmonary sequestrations who received
Neonatal pulmonary sequestration: clinical experience with transumbilical arterial embolization.
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Pulmonary sequestration (PS) is a rare congenital malformation of the lower respiratory tract. The exact natural course of PS is not well understood and there are no well-established treatment guidelines for antenatally diagnosed PS. The aim of this study was to describe clinical outcomes in
Atherosclerosis of aberrant arteries from the left gastric artery into the right intralobar pulmonary sequestration complicated by mycobacterial epithelioid cell granuloma.
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Vascular changes observed in intralobar pulmonary sequestration (PS) have been reported to be similar to those observed in pulmonary hypertension (PH). However, atherosclerosis in the pulmonary artery, which is one of the characteristic arterial changes of PH, has scarcely been reported in PS. Here,
Intralobar pulmonary sequestration supplied by multiple anomalous arteries: report of a case.
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Pulmonary sequestration is abnormal pulmonary tissue that has separated from the normal pulmonary parenchyma, is not connected to the tracheobronchial tree, and is supplied by a systemic artery. We describe herein a case of intralobar pulmonary sequestration found in a 66-year-old man who was
[Diagnosis and surgical treatment of pulmonary sequestration].
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OBJECTIVE
To investigate the classification, incidence, clinical characteristics, diagnosis and surgical treatment of pulmonary sequestration.
METHODS
The clinical data of 23 patients with pulmonary sequestration, 13 males and 10 females, aged 39 (12 - 71), with a course of 3 days to 9 years,
[Bronchopulmonary sequestration: review of 27 cases].
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OBJECTIVE
To explore the clinical manifestations, the diagnosis and the treatment of bronchopulmonary sequestration.
METHODS
Twenty-seven cases of bronchopulmonary sequestration confirmed by histopathological studies were analyzed and related literatures were reviewed.
RESULTS
Among the 27 cases of
Extralobar pulmonary sequestration in a 55-year-old man.
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Pulmonary sequestration is a rare congenital lung malformation that more commonly occurs in the left lung, mainly near the lower mediastinum. It is rarely observed in patients with extralobar sequestration in adulthood. We report the case of a 55-year-old man with recurrent fever and cough lasting
Emergency laparotomy helped the resection of an intralobar pulmonary sequestration with haemorrhagic shock.
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Massive intrapulmonary haemorrhage and haemothorax are uncommon presentations associated with pulmonary sequestration. Here, we describe the case of a 40-year-old man who suffered from high fever and haemoptysis for 1 week before he was admitted to our hospital with a complaint of chest discomfort
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