Case Report

1. Abstract 1.1. Introduction: Lymphangioma is an uncommon benign tumor believed to be the result of diffuse proliferation of lymphatic tissues. Abdominal lymphangiomatosis is a rare disease characterized by infiltration of the intraperitoneal organs with lymphangiomas. Clinical symptoms of this condition are not clear. Pathological, radiological, and clinical evidence are limited for diagnosis. During operation,

1. Abstract The Breast Imaging Reporting and Data System (BI-RADS®) is a standardized system of reporting breast pathology used also for Magnetic Resonance Imaging (MRI). It facilitates clear communication between the radiologist and other physicians as surgeons involved in senology, by providing a lexicon that compares breast gland structures to assessment categories in the management

1. Abstract Auto Immune Thyroiditis (AIT) and Graves’ disease are autoimmune diseases with the opposite state of thyroid function: hypothyroidism and thyrotoxicosis. Typically, thyrotoxicosis can progress to thyroiditis and eventually hypothyroidism. http://dx.doi.org/10.47829/JCMI.2021.51005

1. Abstract A 46-year-old white man, presented to the emergency department with backache for 2 weeks, which aggravated with right upper abdominal pain for 1 day without fever. He was homosexual with normal dietary habits and no history of alcoholism or smoking. Contrast-enhanced CT showed a huge mass with several smaller masses underneath occupying the

1. Abstract Mucus plugs can partially or completely obstruct one or more airways and cause serious consequences, including atelectasis. Invasive ventilation increases the risk for mucus plug formation, since mucociliary clearance is impaired in the presence of the endotracheal tube and because relatively dry gases cause mucosa to produce more mucus. Moreover, ineffective coughing resulting

1. Abstract The treatment of choice in congenital structural cardiopathy, including atrial septal defects, is mostly carried out using a percutaneous approach. The main complications of this approach involve the puncture. Other complications include device migration, shunts, or endocarditis and they are extremely rare. Inhere we present a case of a patient with late Amplatzer-related

1. Abstract Primary and metastatic malignant melanomas represent a rare diagnosis with a small number of described cases. The aggressive nature of the tumor, non -specific symptoms, difficult diagnosis, and no official protocol about the treatment result in poor disease prognosis. chemotherapy, immunotherapy or radiotherapy can be employed. A case of a patient with malignant

1. Abstract Relapsing Polychondritis (RP) is a rare disease characterized by inflammation of cartilage and connective tissues with destructive episodes. Although the pathogenesis is not completely known, there is an autoimmunity in which antibodies against mainly type II collagen play a role.