36591000119102: Teratoma (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Germ cell tumor (disorder)\Teratoma (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3323170018 Teratoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3326771017 Teratoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

5629241000241119 tératome fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Teratoma (disorder)	Associated morphology	Teratoma - category	false	Inferred relationship	Some	1
Teratoma (disorder)	Is a	Germ cell tumor (disorder)	true	Inferred relationship	Some
Teratoma (disorder)	Associated morphology	Teratoma	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fetal sacral teratoma causing disproportion	Is a	False	Teratoma (disorder)	Inferred relationship	Some
Intrapulmonary teratoma	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Teratoma of ovary (disorder)	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Sacrococcygeal teratoma	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Extragonadal teratoma is an extremely rare, benign or malignant germ cell tumor characterized, clinically, by a teratoma presenting in an extragonadal location (e.g. retroperitoneum, mediastinum, craniofacial or sacrococcygeal region, intraosseous, solid organs) and, histologically, by displaying well-differentiated structures, as well as immature elements. Presenting symptoms are variable depending on size and location of tumor.	Is a	True	Teratoma (disorder)	Inferred relationship	Some
A rare neoplastic disease with the presence of a testicular neoplasm composed of several, well-differentiated or immature, tissues derived from one or more of the 3 germinal layers. Patients typically present unilateral (occasionally bilateral) painless testicular swelling or a palpable testicular nodule/mass.	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Fetal sacral teratoma	Is a	False	Teratoma (disorder)	Inferred relationship	Some
Congenital teratoma of nasopharynx (disorder)	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Epignathus is a very rare and life threatening intraoral teratoma, usually arising from the maxilla, mandible, palate or base of skull and invading the cranium, nasopharynx or oral cavity. Epignathus is more commonly seen in females, and presents with various manifestations (depending on the tumour size) including obstructive polyhydramnios in the prenatal period and dyspnoea, cyanosis, cough, difficulty in sucking and swallowing, and rarely vomiting (due to swallowing difficulties) postnatally. When large, they can lead to airway obstruction, asphyxia and death in the neonatal period.	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Benign mediastinal teratoma	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Teratoma of orbit (disorder)	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Benign sacral teratoma (disorder)	Is a	False	Teratoma (disorder)	Inferred relationship	Some
Malignant teratoma	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Benign teratoma of retroperitoneum (disorder)	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Benign teratoma of pineal region (disorder)	Is a	True	Teratoma (disorder)	Inferred relationship	Some
Benign teratoma of umbilical cord (disorder)	Is a	True	Teratoma (disorder)	Inferred relationship	Some
A rare neoplastic disorder characterized by benign metastatic masses increasing in size and number after chemotherapy for non-seminomatous germ cell tumors of testis or ovary. It may present at any time after chemotherapy, with a median occurrence within 24 months after treatment completion. Per definition, the resected specimen exclusively contains mature teratoma components, and serum tumor markers have normalized. The retroperitoneum is the most common site, although almost any other localization has been reported. Increased tumor size may cause mechanical compression of vital organs, with renal dysfunction, bowel ischemia, and biliary obstruction as major complications.	Is a	True	Teratoma (disorder)	Inferred relationship	Some

This concept is not in any reference sets