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
Malattia Leventinese (ML) is an autosomal dominant macular dystrophy with a homogeneous genetic makeup. From an ophthalmic perspective, it can be identified by a radial arrangement of parapapilla deposits, also known as Forni's verrucosities, and by drusen-like deposits in the ma...
Open access
Research Article10.9734/ijmpcr/2025/v18i2419
Eye diseases may lead to visual impairment which is one of the public's most feared disabilities. Tuberculosis is a systemic infectious disease caused by Mycobacterium tuberculosis. Ocular tuberculosis is a rare manifestation of this condition. We report the case of a 36-year-old...
Open access
Research Article10.9734/ijmpcr/2025/v18i2417
We present two cases of barosinusitis with distinct clinical presentations: a 33-year-old flight mechanic developing acute visual blurring from maxillary-ethmoidal-frontal sinusitis and a 30-year-old flight attendant with recurrent maxillary sinus pain exacerbated by allergic rhi...
Open access
Research Article10.9734/ijmpcr/2025/v18i2418
Background: Horner syndrome (HS), a rare neurological condition caused by disruption of the oculosympathetic pathway, can occasionally serve as an early indicator of systemic diseases such as Behçet syndrome (BS). Neuro-Behçet syndrome (NBS) represents a severe manifestation of B...
Open access
Research Article10.9734/ijmpcr/2025/v18i2416