Results 51 to 60 of about 31,298 (246)

A prospective clinico-hematological study in 100 cases of pancytopenia in capital city of India

open access: yesJournal of Applied Hematology, 2014
Context: Pancytopenia is not a disease but a clinico-hematological entity encountered in clinical practice. A prompt intervention is required to avoid complications, which can occur in these patients.
Sweta   +3 more
doaj   +1 more source

A single-center cross-sectional study on the clinical profile of pancytopenia and a novel scoring system for megaloblastic anemia

open access: yesApollo Medicine, 2022
Background: Our study tries to identify the main culprits causing pancytopenia and its typical clinical presentation, along with the clinical and hematological profile of megaloblastic anemia (MGA)-induced pancytopenia, in a tertiary care hospital in ...
Sanjaykumar Somsingbhai Rathwa   +3 more
doaj   +1 more source

Pancytopenia in Lyme disease [PDF]

open access: yesBMJ Case Reports, 2014
We present a 49-year-old man with subacute onset of fever, weakness, shortness of breath, unilateral lower extremity oedema and pancytopenia who was found to have positive serology for Lyme disease. The patient presented with an intravascular haemolytic pattern on laboratory findings where an extensive infectious disease and haematological workup ruled
Raman, Mehrzad, Joseph, Bravoco
openaire   +2 more sources

The Homozygous p.(Arg215Ter) Variant in XRCC2 Is Associated With Atypical Fanconi Anemia Without Major Hematological Abnormalities in Childhood

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Fanconi Anemia (FA) is the most frequent inherited bone marrow failure syndrome. A role for the XRCC2 gene in FA was suspected in 2012 and confirmed in 2016, but only two affected individuals have been described thus far, and no long‐term follow‐up is available.
Sabina Cenciarelli   +11 more
wiley   +1 more source

Bone marrow examination in cases of pancytopenia

open access: yes, 2017
Background: Pancytopenia is a relatively common hematological entity. This study was undertaken to find out the various causes of pancytopenia by bone marrow examination of patients admitted to New civil hospital, Surat, Gujarat, India.Methods: This was ...
Shruti Gheewala   +7 more
core   +2 more sources

Clinicohematological Study of Pancytopenia in a Tertiary Care Hospital of Western Region of Nepal

open access: yesJournal of Nepal Medical Association, 2017
Introduction: Pancytopenia is a relatively common hematological entity and is a manifestation of many illnesses which can be life threatening at times. The severity of pancytopenia and the underlying pathology determine the management and prognosis. This
Dilasma Ghartimagar   +6 more
doaj   +1 more source

Bone Marrow Cellularity in Pancytopenia- A Paradigm of Underlying Pathology

open access: yesNational Journal of Laboratory Medicine, 2023
Introduction: Reduced numbers of all three types of peripheral blood cells characterise the hematologic condition known as pancytopenia. Practical distinction among various causes of pancytopenia is usually clear but some processes are so closely related
Alok Kumar   +4 more
doaj   +1 more source

Histoplasmosis-induced pancytopenia [PDF]

open access: yesBlood, 2012
![Figure][1] A 61-year-old truck driver developed a fever, cough, and shortness of breath requiring oxygen support and antibiotics. He had rheumatoid arthritis controlled with methotrexate and hydroxychloroquine.
Cyrus C, Hsia, Alejandro, Lazo-Langner
openaire   +2 more sources

Reconceptualizing Aplastic Anemia—Seed, Worm, Soil

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
Aplastic anemia (AA) encompasses a group of hematological syndromes often misdiagnosed, resulting in a decrease in the overall blood cell count and representing a form of bone marrow failure. We reinterpret AA based on the “seed, worm, and soil” doctrine.
Xintong Xu   +4 more
wiley   +1 more source

Mucopolysaccharidosis Type 3B in an Adult with Pancytopenia: A Rare Case Report

open access: yes, 2014
Mucopolysaccharidoses are rare hereditary lysosomal storage diseases developing due to dysfunction or deficiencies in enzymes that metabolize long-chain carbohydrates and glycosaminoglycans.
Nihal Güzelay   +3 more
core   +1 more source

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