Partial agenesis of pancreas (Q46346): Difference between revisions

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+CID11:LB21.4
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+Normal rank
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+dki-india-LB21.4
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+Concluído
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+https://pauloleads.com.br/cases-publicos/
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+August 2026Timestamp +2026-08-13T00:00:00Z
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+ICD S353
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Latest revision as of 14:52, 13 August 2026

Partial agenesis of the pancreas is characterised by the congenital absence of a critical mass of pancreatic tissue. The severity of the disease depends on the amount of functional pancreatic tissue present. Pancreatic agenesis is commonly associated with other malformations, in particular pancreaticobiliary duct anomalies, leading to acute or chronic pancreatitis, hyperglycaemia (50% of cases), or, more rarely, polysplenia.

Language	Label	Description	Also known as
default for all languages	LB21.4
English	Partial agenesis of pancreas	Partial agenesis of the pancreas is characterised by the congenital absence of a critical mass of pancreatic tissue. The severity of the disease depends on the amount of functional pancreatic tissue present. Pancreatic agenesis is commonly associated with other malformations, in particular pancreaticobiliary duct anomalies, leading to acute or chronic pancreatitis, hyperglycaemia (50% of cases), or, more rarely, polysplenia.