3B81.6ICD-11 MMS 2026-01
Infarction of spleen
Description
A disease caused by determinants such as trauma, infection, or inherited factors leading to a shortage of oxygen in the spleen. This disease is characterised by death of spleen tissue and loss of function. Confirmation is by medical imaging.
Index terms
- Infarction of spleen
- Spleen phlebothrombosis
- splenic phlebothrombosis
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- Necrotising spleen
- ischemic splenic necrosis
- necrotic spleen
- splenic necrosis
- Splenic haemorrhage
- spleen haemorrhage
- Subcapsular splenic haemorrhage
Excludes
NB91.0– traumatic rupture of spleen
Exclusions from above levels
04– Diseases of the immune system05– Endocrine, nutritional or metabolic diseases18– Complications of pregnancy, childbirth or the puerperium
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19– Certain conditions originating in the perinatal period20– Congenital malformations, deformations or chromosomal abnormalities22– Injury, poisoning or certain other consequences of external causes- http://id.who.int/icd/entity/1000704511 – Human immunodeficiency virus disease
JB64.1– Other diseases of the blood or blood-forming organs or certain disorders involving the immune mechanism complicating pregnancy, childbirth or the puerperium
Foundation children elsewhere
KA83.5– Neonatal haemorrhage originating in spleen
Sibling codes
3B81.0– Tumour-like conditions of spleen3B81.1– Postsurgical asplenia3B81.2– Atrophy of spleen3B81.3– Nontraumatic laceration or rupture of spleen3B81.4– Splenosis3B81.5– Splenic cyst or pseudocyst3B81.7– Infection of spleen3B81.8– Torsion of spleen3B81.9– Fibrosis of spleen3B81.A– Perisplenitis3B81.B– Hypersplenism3B81.C– Chronic congestive splenomegaly3B81.Y– Other specified acquired disorders of spleen3B81.Z– Acquired disorders of spleen, unspecified
Foundation entity
Infarction of spleen – http://id.who.int/icd/entity/2072693588
Part of: 3B81: Acquired disorders of spleen › 03: Diseases of the blood or blood-forming organs