Background
The ease of implantation of the rapid deployment (RD) and sutureless valves has contributed to the adoption of anterior right thoracotomy (ART) approach for aortic valve replacement (AVR).
Aim of the study
This study evaluates the safety and haemodynamic performance of minimally invasive AVR through ART using the RD valves.
Methods
This is a retrospective, single‐center review of a total of 50 consecutive patients who received RD‐AVR through ART.
Results
The median age of patients was 75 years (interquartile range [IQR]: 69‐80), and median Euroscore II was 5.1 (IQR: 2.4‐7.5). ART RD‐AVR was successfully performed in all cases with no conversion to sternotomy, paravalvular leaks or need for valve explantation. The mean size of the implanted valve was 23.2 ± 2.3 mm. In‐hospital mortality was 2%. The mean and maximum pressure gradients across the aortic prosthesis were 10 mm Hg (IQR: 9‐12) and 19 mm Hg (IQR: 16‐23).
Conclusions
Rapid deployment aortic valve replacement can be safely performed through anterior right thoracotomy wit excellent haemodynamic performance and low postoperative complications rate.
BackgroundThoracic outlet syndrome (TOS) is a pathological condition caused by a narrowing between the clavicle and first rib leading to a compression of the neurovascular bundle to the upper extremity. The incidence of TOS is probably nowadays underestimated because the diagnosis could be very challenging without a thorough clinical examination along with appropriate clinical testing. Beside traditional supra-, infraclavicular or transaxillary approaches, the robotic assisted first rib resection has been gaining importance in the last few years.MethodsWe conducted a retrospective cohort analysis of all patients who underwent robotic assisted first rib resection due to TOS at Lucerne Cantonal Hospital and then we performed a narrative review of the English literature using PubMed, Cochrane Database of Systematic Reviews and Scopus.ResultsBetween June 2020 and November 2021, eleven robotic assisted first rib resections were performed due to TOS at Lucerne Cantonal Hospital. Median length of stay was 2 days (Standard Deviation: +/– 0.67 days). Median surgery time was 180 min (Standard Deviation: +/– 36.5). No intra-operative complications were reported.ConclusionsRobotic assisted first rib resection could represent a safe and feasible option in expert hands for the treatment of thoracic outlet syndrome.
Primary pulmonary lymphoepithelioma-like carcinoma (LELC) is a rare tumour that is histologically identical to the lymphoepithelioma originally described in the nasopharynx. It mostly occurs in endemic regions in Asia, where it is associated with Epstein-Barr virus (EBV) infection. The incidence of primary pulmonary LELC is even lower in the Western population, in which an association with EBV is not typically observed. In this report, we present the case of a 78-year-old Caucasian woman who was diagnosed with EBV-positive pulmonary LELC following lingulectomy and histopathological examination of the tumour. Metastasis from the nasopharynx was excluded clinically and radiologically. Due to the absence of regional lymph node involvement, the patient did not receive adjuvant therapy. She remained free of disease at the one-year follow-up. Reporting cases of primary pulmonary LELC in non-Asian patients can help to elucidate the association with EBV infection and its potential implications for diagnosis, treatment, and follow-up.
Teratomas are a type of germ cell tumor that may contain several different types of tissue. Neurofibroma is a benign peripheral nerve sheath tumor with the plexiform type being pathognomonic for neurofibromatosis type 1. We report a case of a 33-year-old woman with a background of Neurofibromatosis type 1 who presented with left-sided chest pain and shortness of breath. She was diagnosed with a large mediastinal mass which was confirmed from a CT-guided biopsy as neurofibroma. Following a multidisciplinary team discussion, she underwent mediastinal mass resection and the final histopathology report revealed mediastinal mature teratoma.
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