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All published articles 522

Isolated Male Epispadias with Continence in a 40 Year Old: A Case Report

Atim T., Akpamgbo C. N., Eniola S. B., Aisuodionoe-Shadrach O. I. & Eze G. C. · International Journal of Medical and Pharmaceutical Case Reports · 2023

Epispadias is part of the bladder exstrophy-epispadias complex; it has a defective dorsal wall of the urethra with potential incompetence of the urinary continence mechanism. Isolated male epispadias is due to failure of the urethral plate to tubularize on the dorsum of the penis...

Open access Research Article 10.9734/ijmpcr/2023/v16i4359

Case of Ceftriaxone-Induced Immune Hemolytic Anemia in an Outpatient Parenteral Antimicrobial Therapy (OPAT) Unit

Jaslyn Maurer, Samantha Ruddy, Monica Bapna, George Rodriguez & Sorana Segal-Maurer · International Journal of Medical and Pharmaceutical Case Reports · 2023

Background: Ceftriaxone is a commonly used antimicrobial agent for the treatment of various infections. It is frequently administered once daily and is an attractive option for use in both in- and out-patient settings. Ceftriaxone-induced immune hemolytic anemia, while rare, can...

Open access Research Article 10.9734/ijmpcr/2023/v16i4357

Neurological Complications of COVID-19 Vaccination: A Case Report of Generalized Convulsive Status Epilepticus

Machlusil Husna, Ria Damayanti & Priyo Atdisuramad · International Journal of Medical and Pharmaceutical Case Reports · 2023

Generalized convulsive status epilepticus (GCSE) is a life-threatening condition characterized by prolonged seizure activity that affects both sides of the brain. Despite its high mortality rate, GCSE is a relatively rare complication of COVID-19 vaccination. In this case report,...

Open access Research Article 10.9734/ijmpcr/2023/v16i4355

Lung Ultrasound to Diagnose Necrotizing Pneumonia in the Pediatric Patient

Rachna Kadakia, Isaac Gordon & Cornelia Muntean · International Journal of Medical and Pharmaceutical Case Reports · 2023

Necrotizing pneumonia, a severe complication of community-acquired pneumonia, poses a significant risk of potentially fatal outcomes if not promptly identified and treated. The current standard of care in the emergency room involves an initial plain radiograph of the chest follow...

Open access Research Article 10.9734/ijmpcr/2023/v16i4356

Saddle Shaped Thrombus at Subclavian-Vertebral Artery Junction

A. K. Sharma & S. Roy · International Journal of Medical and Pharmaceutical Case Reports · 2023

Acute upper limb ischemia is an uncommon but dreaded cardiovascular emergency. Severity of symptoms is dependent upon the site of the arterial occlusion and the extent of the collateral blood supply around the shoulder and elbow region. The most common cause of occlusion in subcl...

Open access Research Article 10.9734/ijmpcr/2023/v16i4354

A Rare Neurological Sequela: Pontine Infarct Conducing to Millard-gubler Syndrome

Hema Ratna Sai Lakshmi Vemana, Nisar Ahmed, Bhagya Aruna Chikkala, Rupa Lavanya Gogulamanda, Priyanka Kandregula, Minisha Nalli & Pavan Kumar Yanamadala · International Journal of Medical and Pharmaceutical Case Reports · 2023

Background: Ventral Pontine Syndrome, likewise called Millard Gubler Syndrome (MGS) or Facial abducens hemiplegia disorder is a neurodegenerative problem that is described by one-sided lesions influencing the basal piece of the caudal pons including fascicles of the abducens and...

Open access Research Article 10.9734/ijmpcr/2023/v16i4353

Yolk Sac Tumor in a 43-Year-Old Woman

Chijioke O. Ezeigwe, Uchenna D. Okudo, Onyeka C. Ekwebene, Emmanuel C. Egwuatu, Daniel C. Anyiam, Jerome C. Okudo, Oyetokunbo Ibidapo-Obe, George U. Eleje, Charlotte B. Oguejiofor, Nkejesus C. Obi & Victor K. Nwodo · International Journal of Medical and Pharmaceutical Case Reports · 2023

Yolk sac tumors are uncommon and demonstrate rapidity in growth in young women. They are the second most common germ cell tumor following dysgerminomas. They are either pure or are associated with another form of germ cell tumor and can be highly polymorphic. Preservation of fert...

Open access Research Article 10.9734/ijmpcr/2023/v16i4351

Spotting the Culprit: A Rare Case of Hematometra in a Menstruating Female with Fraser Syndrome

Sameer Khan, Nevine Macalintal, Katlin Davitt, Jennifer McEachron & Cornelia Muntean · International Journal of Medical and Pharmaceutical Case Reports · 2023

Background: Fraser syndrome is a rare autosomal disorder that is associated with multiple genetic abnormalities. Discussed here is one abnormality associated with the genital tract. Case Description: A 19-year-old female with Fraser syndrome presented to the pediatric emergency d...

Open access Research Article 10.9734/ijmpcr/2023/v16i4352

A Case Report on Recurrent Episodes of Dyselectrolytemia Diagnosed as Gitleman Syndrome

Priyadharshini V., Deepika Ganesh & Rajmahizhan T. · International Journal of Medical and Pharmaceutical Case Reports · 2023

Background: Gitleman syndrome (GS) is also known as familial hypokalaemia-hypomagnesemia, which is a rare genetic disorder. It is an autosomal recessive disease that is characterized by hypokalaemia, hypomagnesemia, metabolic alkalosis, hypocalciuric hypercalcemia and hyperaldost...

Open access Research Article 10.9734/ijmpcr/2023/v16i4350

Vibrio cholerae Bacteraemia: Report of Two Cases

Bhaskar Narayan Chaudhuri, Amrita Basak, Partha Guchhait, Sayan Naskar, Anupam Das & Satadal Das · International Journal of Medical and Pharmaceutical Case Reports · 2023

Aims: Case reports on Vibrio cholerae bacteraemia are extremely rare and thus such cases should be presented for a proper understanding of the mechanism of these rare conditions. Presentation of Cases: One male patient aged 67 years was suffering from vomiting, hiccups, fever wit...

Open access Research Article 10.9734/ijmpcr/2023/v16i4349

Frustrations of Parents/ Guardians of Children Living with Sickle Cell Disease: A Case Series

Samuel N. Osei-Djarbeng, Samuel Osei-Asante & Natasha Asamoah · International Journal of Medical and Pharmaceutical Case Reports · 2023

Aim: To present some frustrations and problems parents/guardians of children living with Sickle Cell Disease go through. Presentation of Reports: We present series of cases of parents and guardians whose children are less than fourteen (14) years of age and have sickle cell disea...

Open access Research Article 10.9734/ijmpcr/2023/v16i4348

A Case Report on Adult - Onset Still’s Disease

Meenatchi R., Karthy C. & Krithika Sri. J. B. · International Journal of Medical and Pharmaceutical Case Reports · 2023

Background: Adult-onset Still's disease (AOSD) is an uncommon systemic inflammatory condition with an unknown cause, presenting with a set of three main symptoms: recurrent high fevers, joint pain (sometimes accompanied by arthritis), and an evanescent skin rash. Case Report: We...

Open access Research Article 10.9734/ijmpcr/2023/v16i4347

Hemophagocytic Lymphohistiocytosis Secondary to Chronic Lymphocytic Leukaemia and Multiple Infections Manifested with Quotidian Pyrexia: A Case Report

D. Fragrance Jemimah, Gency Ann Raju, S. Hariharan & G. Thenmozhi · International Journal of Medical and Pharmaceutical Case Reports · 2023

Hemophagocytic lymphohistiocytosis (HLH) is a rare, life-threatening immune regulatory condition that can cause end-organ damage and death. HLH is clinically characterized by uncontrolled activation of cytotoxic T lymphocytes, natural killer cells, and macrophages that can lead t...

Open access Research Article 10.9734/ijmpcr/2023/v16i4346

Efficacy and Versatility of the Medial Hemisoleus Flap for Complex Middle Third Tibial Defects: A Presentation of 2 Cases

Amine El Harti, Sarah Sabur, Amine Fikry, Ahlam Youssfi, Sarah Karti & Mounia Diouri · International Journal of Medical and Pharmaceutical Case Reports · 2023

Soft tissue injuries involving the middle third of the tibia can present significant clinical challenges, often leading to complications such as infection and nonunion. This article explores the efficacy of the medial hemisoleus flap as a valuable surgical technique for addressin...

Open access Research Article 10.9734/ijmpcr/2023/v16i4345