Homozygous sickle cell anemia and secondary complications: a case study

CJ Yontz, KV Waller - American Society for Clinical Laboratory …, 2011 - clsjournal.ascls.org
A 26-year-old African-American male presented with chest and back pain, fatigue and a
history of the following: homozygous sickle cell anemia, pain crises, stroke, hip replacement …

[HTML][HTML] Acute chest syndrome due to sickle cell disease as a cause of sudden death: Case report and literature review

T González Gaitán - Medicina Legal de Costa Rica, 2024 - scielo.sa.cr
Abstract GONZALEZ GAITAN, Tatiana. Acute chest syndrome due to sickle cell disease as a
cause of sudden death: Case report and literature review. Med. leg. Costa Rica [online] …

[PDF][PDF] Acute chest syndrome, avascular necrosis of femur, and pulmonary embolism all at once: an unexpected encounter in the first-ever admission of a sickle cell …

A Annadatha, D Talwar, S Acharya, S Kumar, V Lahane - Cureus, 2021 - cureus.com
Acute chest syndrome (ACS) is defined as the radiological appearance of pulmonary
infiltrates with fever or respiratory symptoms like chest pain, breathlessness, and cough in a …

Acute chest syndrome, a distinctive manifestation in sickle cell disease–A case study

U Jadhav, R Babu, B Ghewade… - Journal of Datta …, 2020 - journals.lww.com
Acute chest syndrome is the most common cause of death and second most common cause
for hospitalization of the adult population suffering from sickle cell disease. Therefore, it is …

[HTML][HTML] Acute Chest Syndrome and Pulmonary Embolism in Sickle Cell Disease Case Report: About one Case Admitted at the Mixed Medecine and Sickle Cell …

AM Mukuna, MN Timothée, LK Roger, NY Noela… - Open Access Library …, 2024 - scirp.org
Sickle cell disease (SCD), a hereditary genetic disorder marked by abnormal circulating
hemoglobin, presents a spectrum of complications necessitating collaboration among …

VASO-OCCLUSIVE CRISIS IN A PATIENT WITH SICKLE CELL TRAIT

P Neupane, MK Ranjan, RK Yadav… - Journal of Chitwan …, 2023 - jcmc.com.np
Sickle cell trait occurs as a result of inheritance of a normal haemoglobin gene (HbA) from
one parent and a mutated sickle haemoglobin (HbS) gene from another. Unlike the sickle …

A Pediatric Patient with a Complicated History of Sickle Cell Trait

E Nedelcu, JR Wiencek, CC Pierre - Clinical Chemistry, 2022 - academic.oup.com
A 12-year-old White female with a history of sickle cell trait (HbAS), splenectomy, frequent
pain crises, infections, and acute chest syndrome (ACS) presented to the emergency …

[CITATION][C] Myocardial infarction following sickle cell chest syndrome

MA Tanner, MA Westwood… - British journal of …, 2006 - Wiley Online Library
A 21-year-old Afro-Caribbean male with known homozygous sickle cell disease (HbSS) was
admitted to hospital with an acute sickle chest syndrome. He made a steady recovery but …

[HTML][HTML] Pulmonary infarction without fat or thrombo-embolism in sickle cell anaemia

AM Rouxel, JJ Quiot, E Pasquier… - Respiratory Medicine …, 2008 - Elsevier
The aetiology of the acute chest syndrome in sickle cell disease includes: cardiopathy, lung
infection, rib infarct and fat or venous embolism. We report a case where a chest …

“Pseudo-Sickle” Cell Anemia

R Kasmani, WT Gunning, JI Shapiro - The American journal of the …, 2009 - amjmedsci.com
A25-year-old African American woman presented with a chief complaint of generalized pain.
She carried a diagnosis of sickle cell anemia and history of repeated hospitalizations for …