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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.

Bone pain

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

Total: 7

(per page)

PMID (PMCID)
30636638	FEMALE	Middle Aged
	The additional genetic diagnosis of homozygous sickle cell disease in a patient with Waardenburg-Shah syndrome: a case report.
	Rankine-Mullings AE, Serjeant G, Ramsay Z, Hanchard NA, Asnani M. J Med Case Rep. 2019;13(1):10.
	The complications of sickle cell disease she experienced included bone pain, a chronic right leg ulcer, avascular necrosis of her left hip, and symptomatic cholelithiasis.
22348860 (3306268)	OTHER
	Altered mental status and low anion gap in a patient with sickle cell anemia: a case report.
	Wartak SA, Mehendale RA, Freda B, Verma A, Rose DN. J Med Case Rep. 2012;6:72.
	A 50-year-old African American male patient with sickle cell disease presented with refractory anemia, recurrent bone pains and encephalopathy.
19050460	FEMALE	Adult
	Continuous inhaled nitric oxide therapy in a case of sickle cell disease with multiorgan involvement.
	Chang WL, Corate LM, Sinclair JM, van der Heyde HC. J Investig Med. 2008;56(8):1023-7.
	A 27-year-old female with sickle cell disease (HbSS) was admitted presenting with severe bone pain and fever.
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.
	We report a case of bone pain associated with primary hyperparathyroidism in a patient with sickle cell disease.
15495257	MALE	Adult
	Sickle cell crisis associated with hemophagocytic lymphohistiocytosis.
	Kio E, Onitilo A, Lazarchick J, Hanna M, Brunson C, Chaudhary U. Am J Hematol. 2004;77(3):229-32.
	We present a case of an African American male who was first diagnosed with sickle cell disease (SCD) at the age 23 years when he presented with generalized bone pain, fever, and hepatosplenomegaly.
7748367	FEMALE
	Nontraumatic fat embolism syndrome in sickle cell anemia.
	Horton DP, Ferriero DM, Mentzer WC. Pediatr Neurol. 1995;12(1):77-80.
	A 14-year-old girl with sickle cell disease and nephrotic syndrome developed bone pain, followed by pulmonary edema, seizures, coma, and bilateral flaccid paralysis.
6691757	FEMALE	Adult
	Fat embolism in sickle cell disease. Report of a case with brief review of the literature.
	Shapiro MP, Hayes JA. Arch Intern Med. 1984;144(1):181-2.
	It should be suspected in any patient with sickle cell disease in whom unexplained fever, respiratory, and neurologic symptoms typical of fat emboli develop following the onset of bone pain.