Journal of Clinical and Medical Images (ISSN 2640-9615)
(ISSN 2640-9615)
1. Introduction The U.S. healthcare system, herein called “patient” Healthcare, is critically ill, both medically and financially. Of this, there is no dispute. There is strong disagreement about how to cure this patient. Most people look to government to fix the patient. This has not worked despite more than fifty years, innumerable legislative acts, and […]
Curing Patient Healthcare In 2 Images Read More »
1. Summary Eosinophilic gastrointestinal diseases (EGIDs) are rare, im- mune-mediated disorders characterized by eosinophilic infiltra- tion of one or more areas of the gastrointestinal (GI) tract, various gastrointestinal symptoms depending on the affected tract region, as well as depth and extent of eosinophilic infiltration, and the absence of other known causes of eosinophilia.
1. Abstract Brugada syndrome, though rare, poses a significant risk of sudden cardiac death, particularly in young adults, and remains underdiagnosed globally. We present the case of a 22-year-old male initially presenting with a presumed seizure episode, later found to exhibit findings suggestive of type 1 Brugada pattern on his admission electrocardiogram [EKG].
Brugada and Epilepsy: Recurrent Coincidence or Meant to Be? Read More »
1. Abstract Pyothorax-associated lymphoma (PAL) is a rare disease with variations in endemic prevalence. PAL arising from a posttraumatic empyema are a rare occurrence. Here, we report a case of Epstein- Barr virus (EBV)-positive PAL arising from a posttraumatic empyemae. A male patient, 83 years old. Twenty years earlier, the patient fell from a height,
Pyothorax-Associated Lymphoma: A Case Report and Review Read More »
1. Abstract 1.1. Objective: We report the retrospective analysis of three patients with severe COVID-19, with a SpO2 of 87% on average, treated with a co-adjuvant therapy of inhaled ethanol, as well as a review on the use of this therapy in some respiratory diseases.
1. Abstract Orthodontic and surgical technical advances in recent years have resulted in treatment opportunities for a whole range of craniofacial skeletal disorders either in the adolescent or adult patient. In the growing child these can include myofunctional orthodontic appliance therapy or distraction osteogenesis procedures, whilst in the adult the mainstay approach revolves around orthognathic
1. Clinical Images A 48-year-old Moroccan woman with no significant medical history was referred to our institution for evaluation of 4 months history of left flank pain, diarrhea and arthralgia.
Uncommon Endoscopic Presentation in Inflammatory Bowel Diseases Read More »
1. Abstract Rosai-Dorfman-Destombes disease is a very rare benign disorder of histiocyte proliferation with unknown etiology. We report the case of a 41 years old man diagnose with this disease, having had long standing cervical lymphadenopathy increasing in size. This case is presented given the difficulty in diagnosis and surgical management on skin involvement.
Lymphadenopathy Presenting as Rosai- Dorfman- Destombes Disease: A Rare Entity Read More »
1. Abstract A rare cause of foot pain is described in which the diagnostic accuracy of the MRI proved vital in pinpointing the location of the aetiology and subsequently in corrective surgery.
Ganglion Cyst as a Rare Cause of Medial Arch of Foot Pain and Diagnostic Accuracy of MRI Read More »
1. Abstract 1.1. Introduction: Computer-assisted detection (CAD) systems based on artificial intelligence (AI) utilizing convolutional neural networks (CNN) have demonstrated successful outcomes in diagnosing lung lesions in several studies.