Background: Ancient schwannoma is a rare, benign peripheral nerve sheath tumor exhibiting degenerative changes. Its presentation in the submental region is extremely uncommon and may be clinically mistaken for a salivary gland tumor. Case Presentation: We report the case of a 51-...
Open access
Research Article10.9734/ijmpcr/2025/v18i3436
Background: Stevens-Johnson syndrome (SJS) and drug-induced liver injury (DILI) are rare but potentially life-threatening adverse drug reactions. Sulfasalazine is known to cause either condition individually, but their simultaneous occurrence is exceedingly rare. Case Presentatio...
Open access
Research Article10.9734/ijmpcr/2025/v18i3435
Central venous catheter placement is a common procedure, performed on a daily basis. It is relatively a safe procedure, with low complication rate. However serious complications can occur, especially in cases of inadvertent artery cannulation. The consequences can be devastating,...
Open access
Research Article10.9734/ijmpcr/2025/v18i3434
Background: Testicular cancer, while rare, remains the most common solid malignancy among young males aged 14 to 40 years. Early diagnosis is critical for improving outcomes, yet delayed presentation is common. Case Presentation: We describe the case of a 19-year-old male present...
Open access
Research Article10.9734/ijmpcr/2025/v18i3433
Background: Crouzon’s syndrome is a rare autosomal dominant genetic disorder caused by mutations in the FGFR2 gene. It leads to craniosynostosis, where the premature fusion of skull bones results in distinct craniofacial abnormalities. Key clinical features include towering skull...
Open access
Research Article10.9734/ijmpcr/2025/v18i3432
Primary pulmonary synovial sarcoma is a rare and distinct entity, comprising 0.5% of all primary lung malignancies. It typically manifests clinically with cough, chest pain, shortness of breath, or hemoptysis, and a mass lesion may be visible on X-ray or CT scan. Diagnosis is est...
Open access
Research Article10.9734/ijmpcr/2025/v18i3430
Aim: Empyema is a rare complication of pneumonia resulting from the accumulation of pusin the pleural space as a result of impairment of host defense and bacterial virulence. About zero.6% of children laid low with pneumonia progress to empyema as in line with research. Case Pres...
Open access
Research Article10.9734/ijmpcr/2025/v18i3429
Epstein Barr virus (EBV), the most prevalent viruses known to infect humans belongs to the herpes family. The genome of the EBV is the first to be fully sequenced. Infectious mononucleosis is a condition that commonly occurs in adulthood presenting with symptoms such as fever, s...
Open access
Research Article10.9734/ijmpcr/2025/v18i3428
Aims: This case report aims to highlight the systemic complications and clinical challenges associated with Antisynthetase Syndrome (ASyS), a rare autoimmune condition characterized by antibodies targeting aminoacyl-tRNA synthetases. Presentation of Case: A 65-year-old woman with...
Open access
Research Article10.9734/ijmpcr/2025/v18i3427
Iohexol is a typical iodinated radiocontrast medium that is widely used in imaging examinations. The molecular structure of iohexol, which contains iodine, can trigger a complex immune response, leading to anaphylactic reactions that may manifest as cardiovascular instability, re...
Open access
Research Article10.9734/ijmpcr/2025/v18i3426
Background: Oxaliplatin, especially when used in combination with capecitabine (CapeOX), is associated with hepatotoxicity, including hepatic sinusoidal injury. Sinusoidal Obstruction Syndrome (SOS) is a rare but potentially serious adverse effect that can complicate chemotherapy...
Open access
Research Article10.9734/ijmpcr/2025/v18i3425
Mycoplasma pneumoniae is a common cause of community-acquired pneumonia in children, often presenting with varied clinical manifestations ranging from mild respiratory symptoms to severe pneumonia and extrapulmonary complications. Diagnosis of Mycoplasma pneumoniae is often chall...
Open access
Research Article10.9734/ijmpcr/2025/v18i2423
Anemia in patients diagnosed with HIV/AIDS is attributed to generalized bone marrow failure or to autoimmune hemolytic processes. However, the two most frequent causes of anemia in these groups of patients are related to either the cytopathic effect of HIV or the antiretroviral d...
Open access
Research Article10.9734/ijmpcr/2025/v18i2422
Background: Pituitary Stalk Interruption Syndrome (PSIS) is a rare congenital disorder characterized by the absence or thinning of the pituitary stalk, hypoplasia of the anterior pituitary, and ectopic posterior pituitary. This results in panhypopituitarism and related clinical m...
Open access
Research Article10.9734/ijmpcr/2025/v18i2420
Primary Sjogren syndrome is a systemic autoimmune disorder commonly presenting with dryness involving the eyes and mouth due to inflammation and resultant pathology of the lacrimal and salivary glands. Sjogren syndrome is managed by replacing moisture at affected glandular sites...
Open access
Research Article10.9734/ijmpcr/2025/v18i2421