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1348305007: Diffuse idiopathic neuroendocrine cell hyperplasia (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Oct 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5393199015 Diffuse idiopathic neuroendocrine cell hyperplasia (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5393200017 Diffuse idiopathic neuroendocrine cell hyperplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Diffuse idiopathic neuroendocrine cell hyperplasia (morphologic abnormality) Is a Benign epithelial neoplasm true Inferred relationship Some
Diffuse idiopathic neuroendocrine cell hyperplasia (morphologic abnormality) Is a Benign neuroendocrine neoplasm true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
A rare pulmonary neuroendocrine tumor, most often presenting in women over 50 years and non-smokers, characterized by long-lasting cough (>10 years), and less frequently by dyspnea or wheezing. A proportion of patients are asymptomatic, the disease being an incidental finding during routine check-ups. Diffuse pulmonary nodules and mosaic attenuation can be detected by CT-scan however only histopathology can confirm the diagnosis detecting a multifocal hyperplasia of pulmonary neuroendocrine cells (carcinoid tumorlets). Ventilatory dysfunction can be obstructive and less often restrictive, mixed or non-specific. Symptoms can progress slowly but sometimes lead to respiratory failure. It is considered as a precursor for pulmonary carcinoid tumor. Associated morphology True Diffuse idiopathic neuroendocrine cell hyperplasia (morphologic abnormality) Inferred relationship Some 1

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