Asplenia classification: Difference between revisions
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==Overview== | ==Overview== | ||
Asplenia may be classified into two groups based on its cause: [[Congenital]]: Isolated asplenia, heterotaxy syndrome, and [[Acquired]]: Functional asplenia. | |||
==Classification== | ==Classification== |
Revision as of 12:09, 19 July 2021
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Asplenia may be classified into two groups based on its cause: Congenital: Isolated asplenia, heterotaxy syndrome, and Acquired: Functional asplenia.
Classification
Asplenia may be classified into two groups based on its cause:[1] [2]
- Congenital: Isolated asplenia, heterotaxy syndrome.
- Acquired: Functional asplenia.
References
- ↑ MYERSON RM, KOELLE WA (1956). "Congenital absence of the spleen in an adult; report of a case associated with recurrent Waterhouse-Friderichsen syndrome". N Engl J Med. 254 (24): 1131–2. doi:10.1056/NEJM195606142542406. PMID 13322226.
- ↑ Long B, Koyfman A, Gottlieb M (2021). "Complications in the adult asplenic patient: A review for the emergency clinician". Am J Emerg Med. 44: 452–457. doi:10.1016/j.ajem.2020.03.049. PMID 32247651 Check
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