Journal of Clinical and Medical Images (ISSN 2640-9615)

Case Report

Rare Case of Buerger’s Disease with Acute Fulminant Progression to Digital Ischaemia Despite Aggressive Medical Treatment

1. Abstract Buerger’s disease, also known as thromboangiitis obliterans (TAO), is a non-atherosclerotic, segmental inflammatory disease affecting small to medium-sized arteries and veins in the limbs. It is a rare disease seen mostly in young male smokers below 45 years of age. Disease course is typically gradual, progressing from claudication symptoms to rest pain eventually […]

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Inter Aortic-Caval Paraganglioma Simulating a Pancreatic Mass

1. Summary Paraganglioma is a tumor that develops from clusters of neuroendocrine cells located along the vascular and nervous axes called paraganglia. They are present in different locations: the thorax (posterior mediastinum), the abdomen (in the vicinity of the large blood vessels; aorta and vena cava) [1]. Some paragangliomas are secreting, most often catecholamines. They

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Lymphoepithelial Cyst Mimicking Malignant Pancreatic Signs

1. Abstract 1.1. Background: A lymphoepithelial cyst of the pancreas is a rare benign lesion that is difficult to diagnose preoperatively and challenging in distinguishing from potentially malignant cystic pancreatic neoplasms. A diagnostic step-up approach is recommended to clarify the lesion’s dignity and specify a treatment plan.

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Solid Pseudopapillary Tumour of the Pancreas, a Chameleon-like Tumour? High CD138 Expression by a Pseudopapillary and Solid Tumour of the Pancreas Simulating a Plasmacytoma

1. Abstract Solid Pseudopapillary Tumour of the Pancreas (SPTP) is an uncommon tumour that occurs mainly in young women. Its aetiology is unknown with a low potential for malignancy. Its diagnosis is most often difficult by biopsy. Imaging data associated with epidemiological data should be sufficient to conjure up its diagnosis. We report the case

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A Rare Case of Acute Disseminated Encephalomyelitis (ADEM) after Plasmodium Falciparum Infection

1. Abstract Malaria infections have a wide array of both acute and chronic neu- rologic presentations that can create unclear clinical pictures, espe- cially when presenting in a region with low malaria prevalence.1 Neurological complications for the pediatric population can be devastating if not correctly identified and promptly treated.

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Gastroparesis Following Pulmonary Vein Isolation: A Case Report

1. Abstract Gastroparesis is a chronic disorder characterized by delayed gastric emptying after meals in the absence of any mechanical obstructions, especially pyloric stenosis [4]. The main symptoms include early satiety and fullness after a meal, nausea, vomiting, belching and bloating [5]. Gastroparesis is a complication of AF ablation which arises due to iatrogenic damage

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Inflammatory Breast Cancer: A Case Report and Literature Review

1. Abstract A 52-year-old female was admitted to our hospital due to the redness and swelling of the left breast continuing for 1 month. Specialist examination found that the left breast is larger than the right side and the left breast quadrant showed skin redness and orange peel on about 1/3 of the breast. This

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Management of the Patient with Dextrocardia, ASD, VSD and Scoliosis Under General Anesthesia: A Case Report

1. Abstract 1.1. Background: With the new anesthesia methods and developments in pediatric surgery, the life expectancy of patients with congenital heart disease (CHD) has been prolonged. The presence of congenital and cardiac anomalies complicates the management of anesthesia and perioperative difficulties may be experienced for the anesthetist when cardiac or non-cardiac surgeries are planned

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18-F-FDG PET/CT Finding of Intramedullary Spinal Cord Metastases from Cerebellar Medulloblastoma – Case Report

1. Case Presentation A 20- years old female patient, diagnosed case of right cerebellum medulloblastoma, post excision, adjuvant chemotherapy, and radiotherapy in 2018. Presented with right eye swelling in 2021. Brain MRI revealed a right frontal parasagittal mass lesion and left lateral cerebellar mass, highly suggestive of disease recurrence. Total spine MRI showed interval development

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A Case of Lipomyelomeningocele Causing Equinovarus is Reported

1. Abstract 1.1. Background: Lipomyelomeningocele ( LMM) is a congenital factor that causes clubfoot. This disease often develops into adulthood and often has rigid deformities. This is the most difficult orthopedic and functional reconstruction surgery. 1.2. Case Presentation: We report case of stiff clubfoot caused by Lipomyelomeningocele (LMM). Through osteotomy correction and Soft tissue loosening,

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