Evans syndrome is an uncommon autoimmune hematological disorder characterized by the coexistence or sequential development of autoimmune hemolytic anemia and immune thrombocytopenia. Its occurrence with antiphospholipid antibody syndrome, cystic fibrosis, chronic pancreatitis, in...
Open access
Research Article10.9734/ijmpcr/2026/v19i3498
Background: Cerebral Venous Thrombosis (CVT) is an uncommon cerebrovascular disorder with a highly variable clinical spectrum. While headache is the most prevalent symptom, acute and severe visual impairment as the dominant presenting feature is rare and constitutes a neuro-ophth...
Open access
Research Article10.9734/ijmpcr/2026/v19i3497
Cerebral venous sinus thrombosis (CVST) is an uncommon form of intracranial thrombosis characterised by the formation of a blood clot within the cerebral venous drainage system, including the dural venous sinuses, cortical veins, and the deep venous structures such as the vein of...
Open access
Research Article10.9734/ijmpcr/2026/v19i2496
Elevated lactate levels and high anion gap metabolic acidosis are hallmarks of Metformin-associated lactic acidosis, a rare but potentially fatal complication of Metformin therapy. Although the incidence of MALA is low, it carries a significantly high mortality rate, particularly...
Open access
Research Article10.9734/ijmpcr/2026/v19i2495
Background: The long-term ingestion of external corticosteroids can lead to iatrogenic Cushing’s syndrome and are known to be adverse drug reactions that are prevented. There are many nonspecific symptoms associated with iatrogenic Cushing’s syndrome that often mimic other dermat...
Open access
Research Article10.9734/ijmpcr/2026/v19i2494
Pulpal necrosis in permanent teeth with trauma-induced incomplete root development complicates treatment planning because of the presence of an open apex and thin dentinal walls. This case report aimed to evaluate the clinical and radiographic outcomes of regenerative endodontic...
Open access
Research Article10.9734/ijmpcr/2026/v19i2493
Introduction: Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) syndrome represents an uncommon yet potentially fatal clinical condition. Drug-induced hypersensitivity reaction is characterised by fever, rash, haematological abnormalities and multi-organ involvement p...
Open access
Research Article10.9734/ijmpcr/2026/v19i2492
Background: Scleritis is a severe and potentially sight-threatening inflammatory disease of the sclera, most frequently associated with systemic autoimmune disorders. Infectious etiologies are less common but remain clinically significant, particularly those caused by herpes viru...
Open access
Research Article10.9734/ijmpcr/2026/v19i2491
Posterior circulation strokes account for 20-25% of ischemic events, frequently presenting with altered sensorium, dysphagia, and limb weakness that challenge early recognition. Coexisting spinal pathology further complicates diagnosis, mandating comprehensive neuroimaging. A 68-...
Open access
Research Article10.9734/ijmpcr/2026/v19i2490
Metastatic breast cancer represents the most advanced stage, where the accurate and rapid identification of neoplastic cells is essential for clinical management and prognostic assessment. Although immunohistochemistry is the gold standard, flow cytometry emerges as a robust and...
Open access
Research Article10.9734/ijmpcr/2026/v19i2489
Introduction: Infantile hemangiomas (IH) are the most common benign vascular tumors of infancy, typically emerging in the early postnatal period. While most IH follow a self-limiting course, ulceration is a frequent complication, particularly in high-risk anatomical sites such as...
Open access
Research Article10.9734/ijmpcr/2026/v19i2488
Background and Aim: VTE is a serious risk after knee replacement surgery. Poor pain management and unsupervised NSAID use may lead patients to skip anticoagulants, increasing clot risk. This case study explores the consequences of unsupervised consumption of over-the-counter (OTC...
Open access
Research Article10.9734/ijmpcr/2026/v19i2487
Background: Perifoveal Exudative Vascular Anomalous Complex (PEVAC) is a rare retinal disorder characterized by an isolated perifoveal aneurysmal lesion that closely mimics the presentation of exudative choroidal neovascularization (CNV), requiring accurate diagnosis via multimod...
Open access
Research Article10.9734/ijmpcr/2026/v19i2486
Background: Thoraco-omphalopagus conjoined twins present extreme surgical and ethical complexity due to shared thoracoabdominal structures, most notably the liver and chest wall. While hepatic separation has been widely emphasized, the role of chest wall reconstruction as a deter...
Open access
Research Article10.9734/ijmpcr/2026/v19i2485
Introduction: Myelin oligodendrocyte glycoprotein antibody–associated disease (MOGAD) presents with varied neurological features and may mimic other causes of acute myelopathy, making early diagnosis challenging. Case Presentation: A 19-year-old male presented with rapidly progre...
Open access
Research Article10.9734/ijmpcr/2026/v19i2484