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


The un-ending saga of Seronegative autoimmune encephalitis
Deepinder Kaur Maini , Ankita Kumari , Rajiv Anand , Saurabh Arora , Atul Prasad , Nishant Tomar , Anubhav Gupta , Tanzeel Ahmad Wani
Year: 2025
Objective: To characterize the clinical presentation, diagnostic challenges, neuroimaging findings, and treatment response in patients with seronegative autoimmune encephalitis (AIE) presenting as new-onset refractory status epilepticus (NORSE) and to assess the utility of fluorodeoxyglucose positron emission tomography (FDG-PET) and electroencephalogram (EEG) in diagnosisand disease monitoring.Background: NORSE is a life-threatening condition... Continue Reading

Ovarian Teratoma with Bowel Fistula managed non-operatively
Thomas Kirengo , Samra Ali , Samuel Ghattas , Mostafa AbdelKarim , Mohiuddin Kamal , Sabina Kondokhar , Joseph Mechery , Ali Murtada
Year: 2025
Background: Mature ovarian cystic teratomas (MOCT) are the most common benign ovarian tumours. They are mainly asymptomatic (60%) but can in rare cases (<1%) complicate by forming a fistula into adjacent structures such as the bowel. Patients with fistulating ovarian teratomas are typically managed surgically, most often requiring laparotomy.  ... Continue Reading

Mucosa-associated lymphoid tissue lymphoma presenting as intestinal obstruction: a case report
Ahmed Qotb , Meshaal Alenezi , Ahmed Khairy , Mohammed AlJasmi
Year: 2025
Background: Mucosa-associated lymphoid tissue (MALT) lymphoma is a rare variant of extranodal marginal zone B cell lymphoma occurring at mucosal sites. Gastric MALT lymphoma is well-described, but non-gastric MALT lymphomas, particularly small intestinal, ceacal, and appendiceal MALT lymphoma, are rare and present diagnostic problems. Intestinal MALT lymphoma is frequently diagnosed... Continue Reading

Rapid-onset group A streptococcal pyomyositis after minor blunt leg trauma in an immunocompetent adult: a case report
Ketankumar Vegad , Deeksha Deepak
Year: 2025
Background: Pyomyositis is uncommon in temperate regions and is usually caused by Staphylococcus aureus. Infections due to group A Streptococcus (GAS) are rare but can progress rapidly. Case Presentation: A healthy 50-year-old man presented with a three-day history of left-calf pain and swelling two days after minor blunt trauma. He... Continue Reading

Atypical Gastrointestinal Presentation and Overcoming Diagnostic and Therapeutic Challenges in Fulminant Capnocytophaga canimorsus Sepsis
Pushpa Saajan , Ashby Mathew , Anusha Karunasagar , Ehab elghaysha , Fiona Mulyansaka , Shikandhini Visuvanthan
Year: 2025
Background:   Capnocytophaga canimorsus is a fastidious, zoonotic Gram-negative bacillus that can cause rapidly fatal septicaemia. Delays in microbiological diagnosis due to slow growth are common, reducing survival chances. This case uniquely highlights both an atypical gastrointestinal presentation and the resolution of a diagnostic impasse through extended CO₂ incubation triggered... 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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