Journal of Clinical Images and Medical Case Reports
(ISSN 2766-7820) Impact Factor: 2.6
NLM/PubMed ID: 9918266187306676
Indexed in ISI

A 34 year old women consulted in emergency in our department for intense headache with vomiting, and bilateral papilledema in the ophtalmologic examination, in front of these symptoms a brain CT-scan was performed.

In Protein-losing enteropathy (PLE), proteins are lost from the gastrointestinal system exceeding their synthesis by other organs. Proteins entering the gut are degraded into amino acids and reabsorbed but conditions causing inflammation or erosion of the gastrointestinal tract increase mucosal permeability with excessive leakage and poor reabsorption.

Chronic large bowel intussusception in adults in rare with literature limited to scattered case reports. The majority of intussusception occurs in pediatric populations and in the small bowel with etiologies ranging from malignancy to polyps.

Ping-pong fractures are rare congenital skull depressions that occur spontaneously or secondary to birth trauma. We report a case of a neonate born via cesarean section with suction assistance at 39 weeks. A 4 cm left parietal depression was noted at birth.

Interrupted aortic arch (IAA) is a relatively rare congenital vascular malformation, with an incidence of less than 1% among congenital heart diseases (CHD). This condition is classified as a duct- dependent anomaly, wherein blood from the left ventricle fails to flow adequately through the descending aorta, compelling reliance on the right ventricle for perfusion to the lower extremities via the ductus arteriosus.

A 74-year-old female presented with mild exertional shortness of breath and pain between her shoulder blades on a background of chronic cough and occasional haemoptysis. Chest radiography demonstrated an abnormal bulge over the left heart border and subsequent dedicated cardiac computed tomography.

This case describes persistent mediastinal chylothorax following bioprosthetic aortic valve replacement and concomitant pulmonary vein isolation for atrial fibrillation. The chylothorax persisted for more than 30 days after surgery and resolved after lymphangiography.

Localized cervical lymphadenopathy is a rare manifestation of diffuse cutaneous Systemic Sclerosis (dcSSc), and its diagnosis can be challenging given the wide range of diseases associated with this complaint. Clinical, laboratory, imaging and histological assesment are fundamental for accurate clinical reasoning.

Hydatid disease, caused by Echinococcus species, primarily affects the liver and lungs but can occasionally involve unusual anatomical locations. We report a rare case of disseminated hydatidosis in a middle-aged female with an atypical hydatid cyst embedded within the posterior uterine wall.

A 70-year-old man with parkinsonism presented with al- tered sensorium of 3 days duration. He had a history of fever and cough one week back and was admitted in local hospital and had several intravenous fluid infusions. There was no history of alcohol intake.