Tumour-like conditions of spleen

Description

Any condition caused by determinants acquired after birth, in the antenatal period or genetically inherited factors, leading to tumour-like conditions of the spleen. Confirmation is through medical imaging.

Index terms

Tumour-like conditions of spleen
Splenic hamartoma
Inflammatory pseudotumour of spleen

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Sclerosing angiomatoid nodular transformation
SANT - [Sclerosing angiomatoid nodular transformation]

Exclusions from above levels

04 – Diseases of the immune system
05 – Endocrine, nutritional or metabolic diseases
18 – Complications of pregnancy, childbirth or the puerperium

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19 – Certain conditions originating in the perinatal period
20 – Congenital malformations, deformations or chromosomal abnormalities
22 – 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

Sibling codes

3B81.1 – Postsurgical asplenia
3B81.2 – Atrophy of spleen
3B81.3 – Nontraumatic laceration or rupture of spleen
3B81.4 – Splenosis
3B81.5 – Splenic cyst or pseudocyst
3B81.6 – Infarction of spleen
3B81.7 – Infection of spleen
3B81.8 – Torsion of spleen
3B81.9 – Fibrosis of spleen
3B81.A – Perisplenitis
3B81.B – Hypersplenism
3B81.C – Chronic congestive splenomegaly
3B81.Y – Other specified acquired disorders of spleen
3B81.Z – Acquired disorders of spleen, unspecified

Foundation entity

Tumour-like conditions of spleen – http://id.who.int/icd/entity/142317144

Part of: 3B81: Acquired disorders of spleen › 03: Diseases of the blood or blood-forming organs