Most Recent
Thalassemia and hemoglobinopathies in pediatric populations: Prevalence, Diagnostic Insights, and Regional Patterns
Thalassemia and hemoglobinopathies are inherited disorders affecting the structure or production of hemoglobin, leading to varying degrees of anemia and lifelong health impact. Early detection through advanced screening plays a critical role in prevention, counselling, and improved clinical outcomes. Using high-performance liquid chromatography (HPLC), the study identified notable positivity across all age groups, with the highest incidence in children aged 4–9 years. The findings reinforce the importance of early and systematic screening to detect carriers and affected individuals, especially in regions with higher prevalence.
An Incidental Diagnosis of Krukenberg’s Tumor (KT): Exploration beyond the Ovaries
This case report describes an incidental diagnosis of Krukenberg’s Tumor (KT) in a patient whose ovarian enlargement was not evident and whose symptoms mimicked a benign fibroid. The final diagnosis was made only via histopathology, demonstrating characteristic microscopic features. Early and accurate detection via pathology can dramatically alter management and prognosis.
A Missed Diagnosis or Neglected Parental Premarital Counselling of Rare Case of Compound Heterozygous Sickle Cell-Beta+Thalassemia in Patient: Case Report
Sickle cell disease, an inherited haemoglobin disorder can lead to serious health complications if unrecognized. Prompt diagnosis enables appropriate monitoring, counselling, and preventive care for improved long-term outcomes. This case report highlights a rare instance of compound heterozygous HbS β-thalassaemia, a condition with a very low prevalence. The report emphasizes the difficulty in distinguishing compound haemoglobinopathies from isolated conditions and the importance of accurate diagnosis for optimal management.
Flowcytometry Immunophenotyping: Role in Acute Leukemia and Detection of Aberrant Expressions in the Indian Population
Flow-cytometry immunophenotyping is a rapid, precise tool for leukemia classification and detecting aberrant expressions. This enables rapid and accurate lineage classification, which is critical for selecting appropriate cytogenetic/molecular testing, refining prognosis, and guiding timely therapeutic decisions that directly influence patient
Malignant Mixed Germ Cell Tumour of Uterus: A Rare Case Report
Malignant mixed germ cell tumors of the uterus are exceptionally rare, with limited literature guiding diagnosis or management.The case highlights the importance of comprehensive histopathological and immunohistochemical evaluation for accurate diagnosis. Early recognition and multimodal treatment are critical, though prognosis remains guarded.
About Us
Metropolis Healthcare is a leading diagnostic service provider in India. We are a team of dedicated professionals committed to ensuring you and your family receive the most accurate and timely healthcare solutions. We believe in making health care accessible, affordable and evidence-based. Our expert panel are equipped with the latest technology and manned by a certified team of over 4000+ technicians.
In diagnostic services, we have more than three decades of experience servicing diverse stakeholders health advantage packages for men, women and seniors, genetic fitness & corporation in over 650+ tests like Oncology, Neurology, Gynaecology, Haematology, and many more. Our diagnostic services are located in leading doctors and clinics and serve over 15+ cities in India.