Database : MEDLINE
Search on : Bronchogenic and Cyst [Words]
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  1 / 1698 MEDLINE  
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[PMID]: 29510429
[Au] Autor:Zoeller C; Ure BM; Dingemann J
[Ad] Address:Department of Pediatric Surgery, Hannover Medical School, Hannover, Germany.
[Ti] Title:Perioperative Complications of Video-Assisted Thoracoscopic Pulmonary Procedures in Neonates and Infants.
[So] Source:Eur J Pediatr Surg;, 2018 Mar 06.
[Is] ISSN:1439-359X
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:INTRODUCTION: Video-assisted thoracoscopic surgery (VATS) has gained broad acceptance among pediatric surgeons. Today, VATS can be regarded as a routine approach for various conditions in neonates and infants. However, there is a lack of information concerning the complications of thoracoscopic pulmonary surgery in neonates and infants. We aimed to review the available data. PATIENTS AND METHODS: A systematic review of the literature was performed using PubMed. All publications reporting on VATS for pulmonary procedures in neonates and infants up to the age of 1 year were included. Articles were reviewed in detail for occurrence of perioperative complications and their treatment. RESULTS: Nine case series were eligible for analysis. Entities treated included lung sequestration, congenital pulmonary airway malformation, congenital lobar emphysema, and bronchogenic cyst. Case series reported on a total number of 135 patients. Complications occurred in 14 patients (10.4%). The major complication was an accidental transection of the middle lobar bronchus that concluded in a later resection of a prior unaffected lung lobe. Other relevant complications reported were bleeding in four patients (3.0%) and persistent air leak in four cases (3.0%). Infectious complications were reported in four patients (3.0%). Additionally, iatrogenic phrenic nerve paralysis occurred in one patient. There were no deaths related to the VATS technique. In 11 cases (8.1%), conversion to thoracotomy had been necessary. General recommendations on the treatment of complications could not be derived due to small patient numbers and lack of details of the complications reported. CONCLUSION: Reports on major complications of pulmonary VATS in neonates and infants below 1 year of age are scarce. As severe complications such as accidental bronchus transection have been described, feasibility of neonatal/infant VATS cannot be unequivocally confirmed. No literature-based recommendation can be given on the treatment of complications.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1803
[Cu] Class update date: 180306
[Lr] Last revision date:180306
[St] Status:Publisher
[do] DOI:10.1055/s-0038-1636917

  2 / 1698 MEDLINE  
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[PMID]: 29390371
[Au] Autor:Lee HD; Han SH; Park SB; Ko Y; Lee KH
[Ad] Address:Department of Rehabilitation Medicine.
[Ti] Title:An intradural extramedullary bronchogenic cyst in the thoracolumbar spine: A case report.
[So] Source:Medicine (Baltimore);96(50):e9263, 2017 Dec.
[Is] ISSN:1536-5964
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:RATIONALE: We report the symptoms beginning with weakness and the clinical courses of a patient who was diagnosed with an intradural extramedullary bronchogenic cyst. PATIENT CONCERNS: The patient was a 44-year-old man visited the Department of Physical Medicine and Rehabilitation for walking difficulties characterized by limping due to muscle weakness of left lower extremity for 5 months and atrophy in left calf muscle. DIAGNOSES: Lumbar spine MRI was repeated, since radiating pain in the left hip and posterior thigh with low back pain developed 16 months later. Intraspinal mass of T12 and L1 levels that was not found in the first MRI was newly found in the follow-up MRI. INTERVENTIONS: Total tumor removal was conducted with laminectomy. It was finally diagnosed as an intradural extramedullary bronchogenic cyst on the basis of the pathological analysis results. OUTCOMES: His left calf circumference was increased compared to before surgery the radiating pain also disappeared. LESSONS: If the patient's MRI findings are not correlated with the electrophysiologic and physical examination findings, additional MRI should be accompanied with other tests for an early detection.
[Mh] MeSH terms primary: Bronchogenic Cyst/diagnosis
Dura Mater/pathology
Low Back Pain/diagnosis
[Mh] MeSH terms secundary: Adult
Bronchogenic Cyst/diagnostic imaging
Bronchogenic Cyst/pathology
Bronchogenic Cyst/surgery
Dura Mater/surgery
Humans
Laminectomy
Low Back Pain/pathology
Low Back Pain/surgery
Lumbar Vertebrae/pathology
Lumbar Vertebrae/surgery
Magnetic Resonance Imaging
Male
Thoracic Vertebrae/pathology
Thoracic Vertebrae/surgery
[Pt] Publication type:CASE REPORTS; JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180301
[Lr] Last revision date:180301
[Js] Journal subset:AIM; IM
[Da] Date of entry for processing:180203
[St] Status:MEDLINE
[do] DOI:10.1097/MD.0000000000009263

  3 / 1698 MEDLINE  
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[PMID]: 29452079
[Au] Autor:Byers JT; Gertz HE; French SW; Wang L
[Ad] Address:Harbor-UCLA, Department of Pathology, 1000 W. Carson St., Torrance, CA 90509, United States. Electronic address: jtbyers@gmail.com.
[Ti] Title:Case report: Retroperitoneal bronchogenic cyst as a diagnostic dilemma after colon cancer diagnosis.
[So] Source:Exp Mol Pathol;, 2018 Feb 13.
[Is] ISSN:1096-0945
[Cp] Country of publication:Netherlands
[La] Language:eng
[Ab] Abstract:A 52 year-old obese male presented with a moderately differentiated adenocarcinoma of the sigmoid colon. On staging CT, the patient was found to have a cystic lesion in the left retroperitoneum.
[Pt] Publication type:LETTER
[Em] Entry month:1802
[Cu] Class update date: 180216
[Lr] Last revision date:180216
[St] Status:Publisher

  4 / 1698 MEDLINE  
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[PMID]: 29389833
[Au] Autor:Nachef Z; Harris K; Dhillon SS
[Ad] Address:Department of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, State University of New York at Buffalo.
[Ti] Title:Bronchogenic Cyst: Fluid-thrill Sign on Endobronchial Ultrasound.
[So] Source:J Bronchology Interv Pulmonol;, 2018 Jan 31.
[Is] ISSN:1948-8270
[Cp] Country of publication:United States
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1802
[Cu] Class update date: 180201
[Lr] Last revision date:180201
[St] Status:Publisher
[do] DOI:10.1097/LBR.0000000000000473

  5 / 1698 MEDLINE  
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[PMID]: 29266024
[Au] Autor:Pogoriler J; Swarr D; Kreiger P; Adzick NS; Peranteau W
[Ad] Address:Departments of Pathology and Laboratory Medicine.
[Ti] Title:Congenital Cystic Lung Lesions: Redefining the Natural Distribution of Subtypes and Assessing the Risk of Malignancy.
[So] Source:Am J Surg Pathol;, 2017 Dec 20.
[Is] ISSN:1532-0979
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Asymptomatic cystic lung lesions-congenital pulmonary airway malformations (CPAMs), sequestrations, and bronchogenic cysts-are commonly diagnosed prenatally. Indications to resect are to eliminate risk of malignancy or infection. CPAMs consist of a spectrum of malformations, with type 1 historically considered the most common. Mucinous cell clusters, seen almost exclusively in type 1, are premalignant lesions at risk for progression to mucinous adenocarcinoma. We reviewed and classified 2.5 years of consecutive, prenatally diagnosed lesions as extralobar sequestration, intralobar sequestration, type 1 CPAM, type 2 CPAM/bronchial atresia, or "other" to determine the distribution of lesion types and risk of malignancy. One hundred eighty-four lesions in 174 patients showed type 1 CPAM to be least common subtype. Type 1 CPAMs had more severe presentation, infrequently had features of obstruction, and usually had cysts ≥2 cm. Fifteen of eighteen type 1 CPAMs had mucinous cell clusters (total risk, 8%), with mucous cells outside main cyst in 12/15. No pleuropulmonary blastomas were identified. Additional historic cases were reviewed to further evaluate risk of malignancy. Over 14 years, 28 infants with fetal/type 1 lesions were identified, with clusters of mucinous cells in 75% of cases. A total of 9 pleuropulmonary blastomas were diagnosed in 6 patients over 16 years. Contrary to historical studies, type 1 CPAMs are much less common than type 2, likely related to detection of asymptomatic lesions prenatally. A majority of type 1 CPAMs contain mucinous cell clusters. This data is useful in management of patients in centers that do not resect asymptomatic lesions.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171221
[Lr] Last revision date:171221
[St] Status:Publisher
[do] DOI:10.1097/PAS.0000000000000992

  6 / 1698 MEDLINE  
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[PMID]: 29194484
[Au] Autor:Tan GJS; Ooi WM; Law RHF; Nardini M
[Ad] Address:Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.
[Ti] Title:Robotic pericardial patch repair of the bronchus intermedius after bronchogenic cyst removal.
[So] Source:Interact Cardiovasc Thorac Surg;, 2017 Nov 28.
[Is] ISSN:1569-9285
[Cp] Country of publication:England
[La] Language:eng
[Ab] Abstract:Bronchogenic cysts are often asymptomatic mediastinal masses that are usually diagnosed as incidental findings. Surgical resection can be performed with robotic surgery, and if repair of the airway is needed, this can be achieved by direct closure or by applying a pericardial patch. We present a case of a 45-year-old woman diagnosed with a mass in the visceral mediastinum. She had undergone resection adopting a 4-armed, completely portal robotic technique. However, the removal of the cyst had led to a large tear in the bronchus intermedius. The bronchus was then repaired with a 2.4-cm-long pericardial patch sutured with the V-lock sutures. The entire procedure was performed in a total span of 189 min, and the patient was discharged on postoperative Day 2. The robotic platform, with articulated instruments, allowed complex suturing while conversion was not required. To our knowledge, the robotic surgery has not been applied in bronchial repairs by pericardial patches, and this case is the first of its kind.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1712
[Cu] Class update date: 171201
[Lr] Last revision date:171201
[St] Status:Publisher
[do] DOI:10.1093/icvts/ivx382

  7 / 1698 MEDLINE  
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[PMID]: 29171948
[Au] Autor:Canivet A; Lancellotti P
[Ad] Address:Service de Cardiologie, CHU de Liège, Site Sart Tilman, GIGA Cardiovascular Sciences, Université de Liège, Belgique.
[Ti] Title:Syndrome de platypnée-orthodéoxie: Une observation clinique perspicace. [Platypnea-orthodeoxia syndrome : an insightful clinical observation].
[So] Source:Rev Med Liege;72(11):494-498, 2017 Nov.
[Is] ISSN:0370-629X
[Cp] Country of publication:Belgium
[La] Language:fre
[Ab] Abstract:We report the case of a patient admitted to the Intensive Care Unit with dyspnea and refractory hypoxemia after surgical resection of a benign bronchogenic cyst. Etiological research approach excluded conventional postoperative hypoxemia causes. Thereafter a platypnea-orthodeoxia syndrome has been diagnosed. Additional tests will demonstrate the existence of a patent foramen ovale. This diagnosis was suitable with the patient's syndrome and was eligible for percutaneous closure procedure allowing immediate resolution of symptoms and confirming the diagnosis.
[Pt] Publication type:CASE REPORTS; ENGLISH ABSTRACT
[Em] Entry month:1711
[Cu] Class update date: 171124
[Lr] Last revision date:171124
[St] Status:In-Data-Review

  8 / 1698 MEDLINE  
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[PMID]: 29164672
[Au] Autor:Raptis A; Deprez PH; Jouret-Mourin A
[Ad] Address:Department of Pathology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.
[Ti] Title:Resection of an intra-esophageal bronchogenic cyst by endoscopic submucosal dissection.
[So] Source:Dig Endosc;, 2017 Nov 22.
[Is] ISSN:1443-1661
[Cp] Country of publication:Australia
[La] Language:eng
[Ab] Abstract:Bronchogenic cysts are rare foregut abnormalities that arise from aberrant budding of the tracheobronchial tree early in embryological development. They account for 10% to 15% of all primary masses of the mediastinum (1), where they appear predominantly and may compress nearby structures. Intra-esophageal bronchogenic cysts are rare and have only been reported in 23 adult cases since 1981 (2). We report an intra-esophageal bronchogenic cyst that was removed by endoscopic mucosal dissection (ESD). This article is protected by copyright. All rights reserved.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1711
[Cu] Class update date: 171122
[Lr] Last revision date:171122
[St] Status:Publisher
[do] DOI:10.1111/den.12983

  9 / 1698 MEDLINE  
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[PMID]: 29110827
[Au] Autor:Hall NJ; Stanton MP
[Ad] Address:University Surgery Unit, Faculty of Medicine, University of Southampton, Southampton General Hospital, Mailpoint 816, Tremona Rd, Southampton SO16 6YD, UK; Department of Paediatric Surgery and Urology, Southampton Children's Hospital, Southampton, UK. Electronic address: n.j.hall@soton.ac.uk.
[Ti] Title:Long-term outcomes of congenital lung malformations.
[So] Source:Semin Pediatr Surg;26(5):311-316, 2017 Oct.
[Is] ISSN:1532-9453
[Cp] Country of publication:United States
[La] Language:eng
[Ab] Abstract:Congenital lung malformations comprise a group of anatomical abnormalities of the respiratory tree including congenital cystic malformations, bronchopulmonary sequestrations, bronchogenic cyst, bronchial atresia, and congenital lobar emphysema. These anomalies are detected with increasing frequency by pre-natal sonography, but may also present for the first time with symptoms in childhood or later life. When symptomatic, there is little controversy that resection is indicated, which is usually curative. When a lesion is asymptomatic there is greater debate regarding the benefit of resection versus continued observation. This article provides an overview of the spectrum of disorders, the management options available and the long-term outcomes associated with each treatment option.
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1711
[Cu] Class update date: 171107
[Lr] Last revision date:171107
[St] Status:In-Process

  10 / 1698 MEDLINE  
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[PMID]: 29099998
[Au] Autor:Brugha R; Semple T; Cook J; Dusmet M; Rosenthal M
[Ad] Address:Imperial College London, 4615, Population Health and Gene Therapy, London, United Kingdom of Great Britain and Northern Ireland.
[Ti] Title:Two Bronchogenic Cysts Causing Tracheal Stenosis in an Infant.
[So] Source:Am J Respir Crit Care Med;, 2017 Nov 03.
[Is] ISSN:1535-4970
[Cp] Country of publication:United States
[La] Language:eng
[Pt] Publication type:JOURNAL ARTICLE
[Em] Entry month:1711
[Cu] Class update date: 171103
[Lr] Last revision date:171103
[St] Status:Publisher
[do] DOI:10.1164/rccm.201708-1611IM


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