Results 71 to 80 of about 44,817 (277)

Bone marrow evaluation in a pediatric population with pancytopenia in a tertiary care children’s hospital of Nepal

open access: yesJournal of Pathology of Nepal
Background: Pancytopenia, which is characterized by a triad of anemia, leukopenia, and thrombocytopenia, is frequently observed among the pediatric population.
Uma Bhatta   +2 more
doaj   +1 more source

18‐FDG PET in the Evaluation of Therapeutic Response of Necrotizing Otitis Externa

open access: yesThe Laryngoscope, EarlyView.
PET performed well in assessing the therapeutic response of NEO, with excellent sensitivity but low specificity of visual analysis. A complementary quantitative analysis was useful to distinguish between satisfactory and insufficient partial responses. ABSTRACT Objective The duration of antibiotic treatment for necrotizing otitis externa (NEO) and the ...
Lucie Lécolier   +5 more
wiley   +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

Azathioprine-Induced Severe Bone Marrow Suppression

open access: yesCase Reports in Clinical Practice, 2019
Aplastic anemia is characterized by bone marrow failure and pancytopenia. It could be due to autoimmune disorders, radiation, drugs, or chemicals. Drugs that mostly cause aplastic anemia include chloramphenicol, non-steroidal anti-inflammatory drugs ...
Marzie Ghalamkari   +3 more
doaj   +1 more source

Chronic occlusion of the thoracic aorta: a novel cause of pleuropericardial effusions and pancytopenia

open access: yesJournal of Vascular Surgery Cases and Innovative Techniques, 2021
A 57-year-old man had presented with a 6-month history of worsening dyspnea, renal failure, hypertension, pancytopenia, and a continuous machinery murmur.
Sonali R. Gnanenthiran, MBBS, PhD, FRACP, FCSANZ   +4 more
doaj   +1 more source

Fever with pancytopenia: unusual presentation of extrapulmonary tuberculosis: a case report

open access: yesJournal of Medical Case Reports, 2018
BackgroundTuberculosis is a major health problem in the developing world. Diagnosis of extrapulmonary tuberculosis is delayed because the presentation is nonspecific.
Chamara Dalugama, I. Gawarammana
semanticscholar   +1 more source

Mutation profiling in differential diagnosis between TdT‐positive high‐grade/large B‐cell lymphoma and B‐lymphoblastic leukaemia/lymphoma

open access: yesThe Journal of Pathology, EarlyView.
Abstract Terminal deoxynucleotidyl transferase (TdT) is occasionally expressed in large B‐cell lymphoma (LBCL), and this causes difficulty in differential diagnosis from B‐lymphoblastic leukaemia/lymphoma (B‐ALL/LBL). We reviewed 31 cases of TdT‐positive LBCL and B‐ALL/LBL, and their final diagnosis included 19 diffuse large/high‐grade BCLs with MYC ...
Maria‐Myrsini Tzioni   +27 more
wiley   +1 more source

Clinicopathological study of new onset pancytopenia: An experience of largest study from a tertiary care center of western India

open access: yesMedical Journal of Dr. D.Y. Patil Vidyapeeth, 2021
Background: Pancytopenia is characterized by decreased hemoglobin (adult males
Ganesh Pendkur   +4 more
doaj   +1 more source

A Case of Thyrotoxicosis with Pancytopenia.

open access: yesEndocrine Journal, 2001
We report a 49-year-old man with primary hyperthyroidism who presented with pancytopenia. The patient presented with leg edema, sinus tachycardia, cardiomegaly, and pleural effusions, all from congestive heart failure. Laboratory data showed pancytopenia and primary hyperthyroidism; echocardiogram showed diffuse hyperkinesis of the left ventricular ...
Hideji Tanaka   +6 more
openaire   +4 more sources

Ataxia-pancytopenia syndrome with SAMD9L mutations

open access: yesNeurology: Genetics, 2017
Objective: We describe the neurologic, neuroradiologic, and ophthalmologic phenotype of 1 Swedish and 1 Finnish family with autosomal dominant ataxia-pancytopenia (ATXPC) syndrome and SAMD9L mutations.
Sorina Gorcenco   +16 more
semanticscholar   +1 more source

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