FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1290080008: Neuroendocrine neoplasm of pancreas (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Feb 2024. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5266878017 Neuroendocrine neoplasm of pancreas (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5266879013 Neuroendocrine neoplasm of pancreas en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


23 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neuroendocrine neoplasm of pancreas (disorder) Finding site Pancreatic structure (body structure) true Inferred relationship Some 1
Neuroendocrine neoplasm of pancreas (disorder) Is a Neuroendocrine neoplasm, malignant true Inferred relationship Some
Neuroendocrine neoplasm of pancreas (disorder) Is a Malignant neoplasm of pancreas (disorder) true Inferred relationship Some
Neuroendocrine neoplasm of pancreas (disorder) Associated morphology Malignant neuroendocrine neoplasm (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Primary malignant neuroendocrine neoplasm of pancreas (disorder) Is a True Neuroendocrine neoplasm of pancreas (disorder) Inferred relationship Some
A rare neuroendocrine neoplasm of pancreas characterized by morphologically recognizable neuroendocrine and non-neuroendocrine components, each constituting at least 30% of the tumor volume. Based on histopathology, mixed ductal- and mixed acinar-neuroendocrine carcinomas are distinguished. Patients usually present with unspecific symptoms related to tumor growth and/or metastasis, although occurrence of Zollinger-Ellison syndrome has been reported. Resectability of the tumor is the most important prognostic factor. Is a True Neuroendocrine neoplasm of pancreas (disorder) Inferred relationship Some
Neuroendocrine carcinoma of pancreas Is a True Neuroendocrine neoplasm of pancreas (disorder) Inferred relationship Some
A rare neuroendocrine tumor of pancreas characterized by a well-differentiated epithelial pancreatic neuroendocrine neoplasm measuring at least 0.5 cm, without distinct hormonal syndrome. Tumors <0.5 cm are called microadenomas. Microadenomatosis is the multifocal occurrence of microadenomas. Histopathologic examination shows an organoid growth pattern and expression of synaptophysin and chromogranin A on immunohistochemistry. Tumors are often discovered incidentally, or patients may present with symptoms related to local or metastatic tumor spread. Microadenomas are considered benign, while larger tumors may behave in a malignant manner with extrapancreatic spread, metastasis, or recurrence. Is a True Neuroendocrine neoplasm of pancreas (disorder) Inferred relationship Some
Neuroendocrine tumor of pancreas (disorder) Is a True Neuroendocrine neoplasm of pancreas (disorder) Inferred relationship Some

Reference Sets

GB English

US English

Back to Start