Introduction: Guillain–Barré syndrome (GBS) is an uncommon, acute autoimmune condition affecting the peripheral nervous system, marked by rapidly progressive, symmetrical muscle weakness and loss of deep tendon reflexes. It frequently occurs following an antecedent infectious epi...
Open access
Research Article10.9734/ijmpcr/2026/v19i2483
Background: Budd-Chiari syndrome is an uncommon condition characterized by thrombotic or non-thrombotic obstruction of hepatic venous outflow. It commonly presents with hepatomegaly, ascites, and abdominal pain. Its incidence is estimated at 1 in 100,000 to 1 in 2.5 million annua...
Open access
Research Article10.9734/ijmpcr/2026/v19i2482
Aims: To highlight the role of characteristic multifocal inner retinitis identified by multimodal imaging as a crucial diagnostic marker for Mediterranean Spotted Fever (MSF), particularly when early serology is negative. Case Study: A 45-year-old male presented with a one-week h...
Open access
Research Article10.9734/ijmpcr/2026/v19i1481
Introduction: Phenytoin is a widely used antiepileptic drug with a narrow therapeutic index and dose-dependent non-linear pharmacokinetics. Even minor changes in metabolism or protein binding may precipitate toxicity and neurological manifestations may mimic cerebellar or cerebro...
Open access
Research Article10.9734/ijmpcr/2026/v19i1480
Aims: To describe a severe case of Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS) associated with sequential cephalosporin and vancomycin exposure, and to highlight the diagnostic challenges and hematologic and thromboembolic complications encountered during the cl...
Open access
Research Article10.9734/ijmpcr/2026/v19i1479
Spinal anesthesia (SA) is a popular technique of anesthetic for pregnant women undergoing elective cesarean surgery. The purpose of this study was to present a case of delayed onset of spinal anesthesia in a patient undergoing cesarean section and factors associated with delayed...
Open access
Research Article10.9734/ijmpcr/2026/v19i1478
Introduction: Turner syndrome is a chromosomal disorder caused by partial or complete absence of one X chromosome and is commonly associated with short stature, gonadal dysgenesis, and endocrine abnormalities. Primary amenorrhea is a frequent presenting feature in adolescent fema...
Open access
Research Article10.9734/ijmpcr/2026/v19i1477
Left atrial myxoma is the most common benign primary cardiac tumor, typically arising from the interatrial septum. It is associated with nonspecific systemic, embolic, and obstructive symptoms, making early diagnosis and timely intervention essential. Early surgical excision is t...
Open access
Research Article10.9734/ijmpcr/2026/v19i1476
Introduction: Aplastic anemia is a rare but serious hematological disorder characterized by bone marrow failure leading to pancytopenia. The condition often presents with nonspecific symptoms, resulting in delayed diagnosis and an increased risk of life-threatening complications....
Open access
Research Article10.9734/ijmpcr/2026/v19i1475
Background: Diamond blackfan syndrome is a rarest anemic disease with characteristics of small jaw & wide set eyes, etc. It is gentical disorder rating a low incidence rate world wide. The diagnostic criteria is mainly based upon the clinical presentation, laboratory investig...
Open access
Research Article10.9734/ijmpcr/2026/v19i1474
Background: Scleral dellen is a rare, non-infectious complication of pterygium surgery caused by localized scleral dehydration and tear film instability. Although uncommon, delayed diagnosis may lead to severe scleral thinning and uveal exposure. Objective: To describe the clinic...
Open access
Research Article10.9734/ijmpcr/2026/v19i1472
Purpose: To report a case of bilateral asymmetric adult-onset Best vitelliform macular dystrophy (BVMD), emphasizing the role of multimodal imaging—including fundus autofluorescence (FAF), optical coherence tomography (OCT), and OCT angiography (OCTA)—in detecting retinal dysfunc...
Open access
Research Article10.9734/ijmpcr/2026/v19i1473
Langerhans cell histiocytosis (LCH) is a rare hematological disorder that may present in the oral cavity. Intraoral LCH lesions may present as masses, gingivitis, ulcers, gingival bleeding, tooth loss, pain, cysts, leukoplakia or non-healing wounds after surgery or tooth extracti...
Open access
Research Article10.9734/ijmpcr/2025/v18i4470
Aims: To describe the clinical presentation, imaging features, and outcomes of post-traumatic Bruch’s membrane rupture (BMR), emphasizing the importance of long-term surveillance. Presentation of Case: We report three young male patients (ages 18, 24, and 26; mean ≈23 years) pres...
Open access
Research Article10.9734/ijmpcr/2025/v18i4469
Aims: Understanding the epidemiology, pathophysiology, clinical manifestations, causative mutations and management of oculocutaneous albinism by reporting a case of a 7-year-old child affected by this disease Study Design: Case report. Case Report: 7-year-old child presenting ocu...
Open access
Research Article10.9734/ijmpcr/2025/v18i4468