EJMCR Cover Image EISSN: 2520-4998

European Journal of Medical Case Reports

The European Journal of Medical Case Reports (EJMCR) is a peer-reviewed, open-access journal dedicated to publishing high-quality case reports that contribute valuable insights to medical practice. EJMCR highlights unique clinical cases, rare conditions, innovative diagnostic techniques, and unexpected outcomes, providing a platform for clinicians and researchers to share knowledge and improve patient care worldwide. 

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EJMCR now accepts Videos as supplement to the case reports — highlighting novel techniques, surgical procedures, and intriguing ultrasound findings.
Journal Metrics
Acceptance rate
39%
Initial decision
7 Days
Final decision
45 Days
Acceptance to online publishing
12 Days

Articles


Felty's Syndrome Preceding Rheumatoid Arthritis in a Patient with a History of Rheumatic Fever: A Case Report 
Alma Almadani , Dania Sulaiman , Maysoun Kudsi , Ameen Suliman
Year: 2026
Background: Felty's syndrome is a rare condition affecting 1–3% of patients with rheumatoid arthritis. It typically arises after a prolonged course of RA. Although rheumatic fever and RA may share overlapping features, they are distinct entities; their co-occurrence in a patient is rare and considered coincidental. Case presentation: A 27-year-old... Continue Reading

Breast undifferentiated (pleomorphic) high-grade carcinoma - a case report
Rudainy Kaddoura , Salim Al Rahbi , Zakiya Al Ajmi , Hiba Al Mahruqi
Year: 2026
Background: Pleomorphic carcinoma of the breast is a rare and aggressive histologic variant of invasive breast carcinoma characterized by the presence of highly atypical, bizarre, pleomorphic giant cells. It typically portends a poor prognosis and poses diagnostic challenges due to its undifferentiated morphology. Case Presentation: We report the case of... Continue Reading

Duplication of the 15q11-13 region in a Moroccan patient with autism, intellectual deficiency and absence of speech - A case report 
Fakir Zineb , Tazzite Amal , Berrada Sarah , Dehbi Hind
Year: 2026
Background: The 15q11.2–q13 duplication syndrome (OMIM: 608636) is a rare autosomal dominant neurodevelopmental disorder caused by genomic rearrangements within a highly unstable chromosomal region prone to low-copy repeat–mediated duplications. This region contains imprinted genes involved in Angelman and Prader–Willi syndromes, making the parental origin relevant to its pathogenicity. Clinically, affected... Continue Reading

Acquired Horner Syndrome Secondary to Cervical Disc Herniation.
Daniel Rodrigues , Beatriz Rosa , Carolina Oliveira , Laura Caine , Elsa Goncalves , Marcia Ribeiro
Year: 2026
Background Horner syndrome (HS), defined by the triad of ptosis, miosis, and facial anhidrosis, arises from disruption of the oculosympathetic pathway at any point along its course. The most frequently documented causes include trauma, neoplasms, and iatrogenic injury. Conversely, cervical myelopathy resulting from disc herniation is an uncommon etiology of... Continue Reading

Strengthening Antimicrobial Stewardship Through Regular Interventions: A Two-Cycle Clinical Audit in a District General Hospital in the United Kingdom
Pushpa Saajan , Shayi Shali , Ashica Joshy , Mahboba Muhib , Anusha Krunasagar , Sandra Shali , Shikandhini Visuvanthan
Year: 2026
Background: Antimicrobial resistance (AMR) is a growing global health crisis driven by inappropriate antibiotic use, prolonged treatment, and inadequate documentation of prescribing rationale. Optimizing antimicrobial use through hospital-based stewardship interventions is a clinical priority to improve outcomes and curb resistance. This audit evaluated whether structured pharmacist–microbiologist interventions could enhance compliance... Continue Reading
Primary adrenal malignancies in Oman in the last decade (2014-2023)
Primary adrenal malignancies in Oman in the last decade (2014-2023)

Adrenal gland malignancies are rare but aggressive endocrine tumors. For instance, adrenocortical carcinoma (ACC), a primary adrenal cortical cancer, has an incidence of only about 0.7-2 cases per million population per year. In Oman and the broader Middle East, literature on adrenal malignancies is especially scarce, often confined to single case reports or small series. This study aimed to observe the primary (non-metastatic) adrenal malignancies managed at the study center over the last decade (2013–-2023).

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