Tumors of the broad ligament: what and when to suspect such rare location.

Although secondary involvement of the broad ligament by malignant tumors arising elsewhere in the abdomen and pelvis is common, primary tumors in this location are rare. Tumors of the broad ligament can be of mesenchymal and mixed nature, such as leiomyoma, the most common neoplasm; epithelial tumors of Müllerian type, imposing a challenge to differentiate them from other adnexal masses; unique tumors from mesonephric origin; and tumor-like lesions. Most neoplasms in this region, whether benign or malignant, usually present clinically with vague symptoms and are often discovered during a routine gynecological examination.

Congenital systemic venous return anomalies to the right atrium review.

Congenital anomalies of the systemic venous return to the right atrium are rare and stem from variations in the embryogenesis of the venous system. They are usually asymptomatic, and such the major clinical significance of their recognition is to prevent misdiagnosis, in addition to some having technical implications on invasive procedures.Typically, the venous blood from the upper half of the body is carried by the right-sided, superior vena cava (SVC), and some common congenital abnormalities found are persistent left SVC, SVC duplication, anomalous drainage of the brachiocephalic veins, or interruption of the SVC.

Derivation and external validation of the SHIeLD score for predicting outcome in normotensive pulmonary embolism.

Background: Identifying patients with normotensive pulmonary embolism (PE) who may benefit from thrombolysis remains challenging. We sought to develop and validate a score to predict 30-days PE-related mortality and/or rescue thrombolysis.

Methods: We retrospectively assessed 554 patients with normotensive PE.