Difference between revisions of "Sickle cell disease"

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'''Sickle cell disease''' is a heritable [[haematopathology|haematologic]] disorder associated with serious pathologies.
'''Sickle cell disease''', also '''sickle cell [[anemia]], is a heritable [[haematopathology|haematologic]] disorder associated with serious pathologies.


==Liver==
==Liver==

Revision as of 14:43, 30 July 2011

Sickle cell disease, also sickle cell anemia, is a heritable haematologic disorder associated with serious pathologies.

Liver

  • Cirrhosis and liver failure.[1]

Spleen

  • It may lead to auto infarction - result in hypofunction.
    • Splenectomy have increased risk from polysaccharide encapsulated bacteria, i.e. Neisseria meningitis, Haemophilus influenzae, and Streptococcus pneumoniae.

Gallbladder

  • Pigment stones.

Kidney

See also

References

  1. Hurtova, M.; Bachir, D.; Lee, K.; Calderaro, J.; Decaens, T.; Kluger, MD.; Zafrani, ES.; Cherqui, D. et al. (Apr 2011). "Transplantation for liver failure in patients with sickle cell disease: challenging but feasible.". Liver Transpl 17 (4): 381-92. doi:10.1002/lt.22257. PMID 21445921.
  2. Davis CJ, Mostofi FK, Sesterhenn IA (January 1995). "Renal medullary carcinoma. The seventh sickle cell nephropathy". Am. J. Surg. Pathol. 19 (1): 1–11. PMID 7528470.