Sickle cell anemia

Sickle cell anemias are chronic hemolytic diseases that may induce three types of acute accidents: severe anemia, severe bacterial infections, and ischemic vasoocclusive accidents (VOA) caused by sickle-shaped red blood cells obstructing small blood vessels and capillaries. Many diverse complications can occur.

Back pain

An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) localized to the back.


Total: 9

                      


(per page)
PMID (PMCID)
24855399
(4020897)
OTHER
Back pain: the sole of presentation of sickle cell disease.
Osman S, Khan S, Hendaus MA.
J Blood Med. 2014;5:49-53.
Hence, sickle cell disease with vaso-occlusive crisis should be incorporated into the list of differential diagnoses in children with back pain.
24855399
(4020897)
OTHER
Back pain: the sole of presentation of sickle cell disease.
Osman S, Khan S, Hendaus MA.
J Blood Med. 2014;5:49-53.
Back pain: the sole of presentation of sickle cell disease.
21768865
FEMALE Infant, Newborn
Epidural analgesia for treatment of a sickle cell crisis during pregnancy.
Winder AD, Johnson S, Murphy J, Ehsanipoor RM.
Obstet Gynecol. 2011;118(2 Pt 2):495-7.
A 20-year-old African American with sickle cell disease presented at 29 4/7 weeks of gestation with severe, debilitating leg and back pain.
21657139
MALE Adult
Homozygous sickle cell anemia and secondary complications: a case study.
Yontz CJ, Waller KV.
Clin Lab Sci. 2011;24(2):78-84.
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 following avascular necrosis of the femoral head, priapism, chronic transfusions, iron overload, hypertension, migraine headaches, port infections, depression and type II diabetes.
19091280
MALE Adult
Acute splenic sequestration in an adult with hemoglobin S-C disease.
Rivera-Ruiz M, Varon J, Sternbach GL.
Am J Emerg Med. 2008;26(9):1064.e5-8.
Acute splenic sequestration crisis is a common, potentially life-threatening complication of sickle cell anemia in children that is uncommon in adults.We present the case of a 44-year-old gentleman with undiagnosed hemoglobin S-C disease who developed intense back pain, marked abdominal distension, systemic inflammatory response syndrome, and multisystem organ failure that first presented as acute splenic sequestration crisis.
18380379
MIXED_SAMPLE Child
[Complaints of back pain in childhood: find curable causes].
Haveman LM, van Es HW, ten Berge-Kuipers M.
Ned Tijdschr Geneeskd. 2008;152(7):353-8.
Three children, a 13-year-old boy and a 3-year-old and 6-year-old girl, were presented to the hospital with back pain, caused by Scheuermann's disease, spondylodiscitis and sickle cell disease, respectively.
18380379
MIXED_SAMPLE Child
[Complaints of back pain in childhood: find curable causes].
Haveman LM, van Es HW, ten Berge-Kuipers M.
Ned Tijdschr Geneeskd. 2008;152(7):353-8.
Various causes of back pain in children can be distinguished: mechanical problems, infections of the lumbar spine, neoplasia, inflammation, and other causes, such as sickle cell disease.
17939320
MALE Child
Diagnostic and treatment difficulties in systemic lupus erythematosus coexisting with sickle cell disease.
Ogunbiyi AO, George AO, Brown O, Okafor BO.
West Afr J Med. 2007;26(2):152-5.
We present an 8-year-old boy with sickle cell disease who presented with recurrent fever, back pains, and 'cutaneous eruptions' to multiple drugs.
16882790
FEMALE
Primary hyperparathyroidism mimicking vaso-occlusive crises in sickle cell disease.
Krishnamoorthy P, Alyaarubi S, Abish S, Gale M, Albuquerque P, Jabado N.
Pediatrics. 2006;118(2):e537-9.
A 17-year-old girl with sickle cell disease (SS phenotype) was seen for bilateral knee and back pain.