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1186735007: Mixed neuroendocrine-non neuroendocrine neoplasm of pancreas (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4667510018 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4667511019 A rare neuroendocrine neoplasm of pancreas characterised by morphologically recognisable neuroendocrine and non-neuroendocrine components, each constituting at least 30% of the tumour volume. Based on histopathology, mixed ductal- and mixed acinar-neuroendocrine carcinomas are distinguished. Patients usually present with unspecific symptoms related to tumour growth and/or metastasis, although occurrence of Zollinger-Ellison syndrome has been reported. Resectability of the tumour is the most important prognostic factor. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4667506016 MiNEN (mixed neuroendocrine-non neuroendocrine neoplasm) of pancreas en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4667507013 Mixed neuroendocrine-non neuroendocrine neoplasm of pancreas (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667508015 Mixed neuroendocrine-non neuroendocrine neoplasm of pancreas en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667509011 Pancreatic mixed neuroendocrine-non-neuroendocrine neoplasm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7723521000241115 tumeur mixte neuroendocrine et non neuroendocrine du pancréas fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7723531000241118 néoplasme mixte neuroendocrine et non neuroendocrine du pancréas fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428881001000118 Gemischte neuroendokrine/nicht neuroendokrine Neoplasie des Pankreas de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
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 néoplasme neuroendocrine malin false 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 Malignant neoplasm of pancreas (disorder) false 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 Neuroendocrine tumor of pancreas (disorder) false 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. Finding site Pancreatic structure (body structure) true Inferred relationship Some 1
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. Associated morphology A mixed epithelial neoplasm that is composed of both neuroendocrine and non neuroendocrine components with variable proportions for each component. true Inferred relationship Some 1
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 Malignant epithelial neoplasm (disorder) true 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 Neuroendocrine neoplasm of pancreas (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Mixed ductal-neuroendocrine carcinoma of pancreas Is a True 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. Inferred relationship Some
Primary mixed acinar endocrine-ductal carcinoma of pancreas (disorder) Is a True 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. Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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