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Congenital anomalies of respiratory system are quite diverse and not all of them are subject to surgical treatment. One example is accessory lobe of the azygos vein. This anomaly usually has no clinical manifestations and requires only follow-up, as well as attention in surgery on the right half of the chest for some other disease.

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Objective: Coronary artery, aortic valve, and descending aorta calcification (CAC, AVC, DAC) are manifestations of atherosclerosis, and cardiac epicardial adipose tissue (EAT) indicates heart adiposity. This study explored the association between cardiac adipose tissue and cardiovascular calcification in participants with long-standing T1D.

Methods: EAT and intra-thoracic adipose tissue (IAT) were measured in 100 T1D subjects with cardiac computed tomography (CT) scans in the EDIC study.

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A rare case report: Gallbladder-associated ectopic liver tissue: Challenges, insights, and surgical considerations.

Int J Surg Case Rep

February 2024

General Surgery Department, Military Hospital of Tunis, Mont Fleury-1008, Tunis, Tunisia; Faculty of Medicine of Tunis, 15, Djebel Lakhdhar Street - 1007 Bab Saadoun, Tunis, Tunisia.

Introduction And Importance: Ectopic liver tissue (ELT), a rare anomaly distinct from accessory liver, challenges conventional embryonic morphogenesis. Unlike the latter, ELT lacks a connection to the main liver, showcasing an unusual growth of normal liver tissue beyond its customary location. This peculiarity poses clinical and radiological challenges for surgeons throughout their careers, particularly during laparoscopic or open procedures.

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Sarcoidosis is a systemic disorder characterized by the aberrant development of granulomatous inflammation within various organs in the body. In over 90% of cases, sarcoidosis typically manifests initially in the intra-thoracic region, characterized by pulmonary involvement or mediastinal lymphadenopathy. It is rare for sarcoidosis to manifest exclusively as extra-thoracic involvement and even more rarely for hypercalcemia to be the only initial sign.

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Article Synopsis
  • Non-bacterial thrombotic endocarditis is a rare condition that can be challenging to diagnose early, which is essential for effective treatment.
  • A 75-year-old male presented with acute lower limb ischemia, revealing complications related to prior anticoagulation treatment for a pulmonary embolism, and was later found to have a malignant lung tumor.
  • The diagnosis of non-bacterial thrombotic endocarditis was supported by the patient's clinical history, imaging results, and the presence of thrombosis without signs of infection, leading to a favorable outcome with surgical intervention and further oncology care.
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