Publications by authors named "F Y Dieng"

Article Synopsis
  • The study focused on managing acute pain in adults with sickle cell disease (SCD), particularly during vaso-occlusive crises (VOC), which occur when sickle cells block microvessels, leading to severe pain.* -
  • An analysis of 118 cases revealed that most patients (86.61%) had the SS sickle cell phenotype, with predominant pain in the lower limbs and spine, and a majority experiencing intense to unbearable pain.* -
  • The findings underscore the effectiveness of multimodal analgesia as a treatment approach, while also indicating significant variability in pain management practices, suggesting a need for tailored recommendations.*
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The Hodgkin variant Richter syndrome (HvRS) is an infrequent complication occurring in 1% of lymphocytic lymphoma/chronic lymphocytic leukemia patients. We report a case of HvRS diagnosed in Sub-Saharan Africa. A 63-year-old patient was consulted for the investigation of an abdominal mass that had been evolving for 5 years prior to admission.

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SUMMARYCOVID-19 infection has emerged as a comorbidity that can significantly increase morbidity and mortality in sickle cell patients with ACS (acute thoracic/chest syndrome). The aim of our study was to assess COVID-19-related morbidity and mortality in sickle cell patients with ACS. This was a retrospective, descriptive study of patient records followed over a 36-month period from January 2020 to December 2022.

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Objectives: The aim of this study was to describe the morbidity and mortality of homozygous sickle cell disease after the age of 40.

Methods: This was a cohort study of 209 patients followed from 1994 to 2022. All hemoglobin electrophoresis-confirmed SS sickle cell patients over 40 years were included.

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