56329008: Pituitary structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Anatomical structure which has as its parts a heterogeneous collection of organs, organ parts, cells, cell parts or body part subdivisions that are adjacent to, or continuous with one another; does not constitute a cell part, cell, tissue, organ, or body part subdivision.\Structure of anatomical compartment (body structure)\Intracranial structure\Brain structure\Brain part\Brain region\Supratentorial brain\Supratentorial brain part\The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.\Structure of diencephalon\Diencephalon part\Pituitary and/or pineal structures (body structure)\Pituitary structure

\Gland structure (body structure)\Endocrine gland structure (body structure)\Pituitary and/or pineal structures (body structure)\Pituitary structure

\Body region structure\Body part structure\Upper body structure\Upper body part structure\Structure of head and/or neck (body structure)\Head structure\Head part\Intracranial structure\Brain structure\Brain part\Brain region\Supratentorial brain\Supratentorial brain part\The cerebrum is the regional structure of the brain, which is the adult equivalent of the forebrain or prosencephalon. It is constituted by the structural derivatives of the telencephalon and diencephalon including the cerebral hemispheres, epithalamus, thalamus, hypothalamus, lateral ventricles and third ventricle. This definition is harmonious with the Federation of Association of Anatomist Second Edition (2019) Part V Terminologia Anatomica.\Structure of diencephalon\Diencephalon part\Pituitary and/or pineal structures (body structure)\Pituitary structure

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Pituitary structure	Is a	Pituitary and/or pineal structures (body structure)	true	Inferred relationship	Some
Pituitary structure	Is a	Hypothalamic structure	false	Inferred relationship	Some
Pituitary structure	del af	Entire diencephalon	false	Additional relationship	Some
Pituitary structure	del af	Entire endocrine system	false	Additional relationship	Some
Pituitary structure	Is a	Hypothalamus part	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Colloid cyst of pituitary gland (disorder)	Finding site	False	Pituitary structure	Inferred relationship	Some	1
Invasive pituitary adenoma	Finding site	False	Pituitary structure	Inferred relationship	Some	1
Colloid cyst of pituitary gland (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Functionless pituitary neoplasm (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Invasive pituitary adenoma	Finding site	False	Pituitary structure	Inferred relationship	Some	1
Functioning pituitary neoplasm (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Pituicytoma	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Familial isolated pituitary adenoma	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Ectopic pituitary tissue	Finding site	False	Pituitary structure	Inferred relationship	Some	2
Congenital absence of pituitary gland	Finding site	False	Pituitary structure	Inferred relationship	Some	2
Accessory pituitary gland	Finding site	False	Pituitary structure	Inferred relationship	Some	2
Congenital anomaly of pituitary gland (disorder)	Finding site	False	Pituitary structure	Inferred relationship	Some	2
Pharyngeal pituitary tissue	Finding site	False	Pituitary structure	Inferred relationship	Some	4
Ectopic pituitary tissue	Finding site	True	Pituitary structure	Inferred relationship	Some	1
A rare pituitary deficiency characterized by herniation of the subarachnoid space into the sella turcica, resulting in flattening of the pituitary gland and endocrine dysfunction. Most common endocrine abnormalities are hyperprolactinemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhea, obesity, and visual disturbances, among others.	Finding site	True	Pituitary structure	Inferred relationship	Some	2
Choroideremia co-occurrent with hypopituitarism	Finding site	False	Pituitary structure	Inferred relationship	Some
Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy.	Finding site	False	Pituitary structure	Inferred relationship	Some
Hypopituitarism following procedure (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	2
Familial isolated pituitary adenoma	Finding site	False	Pituitary structure	Inferred relationship	Some	2
Choroideremia co-occurrent with hypopituitarism	Finding site	False	Pituitary structure	Inferred relationship	Some	1
Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy.	Finding site	True	Pituitary structure	Inferred relationship	Some	1
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia.	Finding site	False	Pituitary structure	Inferred relationship	Some	6
Hypopituitarism due to radiotherapy	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Pharyngeal pituitary tissue	Finding site	True	Pituitary structure	Inferred relationship	Some	2
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia.	Finding site	True	Pituitary structure	Inferred relationship	Some	2
A rare midline cerebral malformation disorder with characteristics of duplicated pituitary stalks and/or glands within duplicated sella. Patients may present various degrees of facial dysmorphism and endocrine abnormalities, including precocious puberty, hypogonadism, hypothyroidism and/or hyperprolactinaemia, as well as associated congenital anomalies such as cleft lip/palate, bifid nasal bridge/tongue/uvula, hypothalamic enlargement with or without hamartoma, nasopharyngeal tumours, corpus callosum agenesis/hypoplasia, basilar artery duplication, and/or vertebral defects (in particular duplication of the odontoid process).	Finding site	True	Pituitary structure	Inferred relationship	Some	1
A rare mixed functioning pituitary adenoma with characteristics of co-secretion of growth hormone and prolactin, which manifests with signs and symptoms of both acromegaly and hyperprolactinaemia.	Finding site	True	Pituitary structure	Inferred relationship	Some	1
A rare acquired pituitary hormone deficiency characterized by the presence of rare benign tumor in the sellar region. Clinical presentation is either acute or insidious and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances and pituitary dysfunction.	Finding site	True	Pituitary structure	Inferred relationship	Some	1
A rare acquired pituitary hormone deficiency characterized by the presence of rare benign tumor in the sellar region. Clinical presentation is either acute or insidious and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances and pituitary dysfunction.	Finding site	True	Pituitary structure	Inferred relationship	Some	2
A rare acquired pituitary hormone deficiency characterized by combination of headache, visual field defects that correlate with cyst size and pituitary dysfunction. Most frequent hormonal manifestations are hypogonadism with amenorrhea/impotence or low libido and galactorrhea.	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Septo-optic dysplasia sequence (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Malignant pituitary blastoma (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Hypopituitarism caused by drug (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Epidermoid cyst of pituitary gland (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Transsphenoidal partial excision of neoplasm of pituitary gland (procedure)	Procedure site - Direct (attribute)	False	Pituitary structure	Inferred relationship	Some	1
Transsphenoidal total excision of neoplasm of pituitary gland (procedure)	Procedure site - Direct (attribute)	True	Pituitary structure	Inferred relationship	Some	1
Endoscopic endonasal transsphenoidal total excision of neoplasm of pituitary gland	Procedure site - Direct (attribute)	True	Pituitary structure	Inferred relationship	Some	1
Endoscopic endonasal transsphenoidal partial excision of neoplasm of pituitary gland	Procedure site - Direct (attribute)	False	Pituitary structure	Inferred relationship	Some	1
A benign tumor invasive into adjacent structures.	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Adenocarcinoma of pituitary gland	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Xanthogranulomatous hypophysitis (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Autoimmune hypopituitarism (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Hypopituitarism due to granulomatous disease	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Hypopituitarism due to metabolic disease (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Hypopituitarism due to vascular disorder	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Immunoglobulin G4 related hypophysitis (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Incision and exploration of pituitary gland	Procedure site - Direct (attribute)	True	Pituitary structure	Inferred relationship	Some	2
Microprolactinoma	Finding site	True	Pituitary structure	Inferred relationship	Some	2
Macroprolactinoma	Finding site	True	Pituitary structure	Inferred relationship	Some	2
Prolactinoma	Finding site	True	Pituitary structure	Inferred relationship	Some	2
Pituitary hypertrophy	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Pituitary degeneration	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Avascular necrosis of pituitary gland (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Isolated deficiency of pituitary hormone (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Metastatic carcinoma to pituitary (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Metastatic adenocarcinoma to pituitary gland (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Primary adenocarcinoma of pituitary gland (disorder)	Finding site	True	Pituitary structure	Inferred relationship	Some	1
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor.	Finding site	True	Pituitary structure	Inferred relationship	Some	1
Structure of transplanted pituitary gland (body structure)	Is a	True	Pituitary structure	Inferred relationship	Some
Excision of neoplasm of pituitary (procedure)	Procedure site - Direct (attribute)	True	Pituitary structure	Inferred relationship	Some	1
Magnetic resonance imaging of pituitary gland (procedure)	Procedure site - Direct (attribute)	True	Pituitary structure	Inferred relationship	Some	1
Malignant neoplasm of pituitary and hypothalamus	Finding site	True	Pituitary structure	Inferred relationship	Some	2

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
93667018	Pituitary gland	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
93669015	Hypophysis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
497589011	Pituitary structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
794829019	Pituitary structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3027151000005111	pituitær struktur	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)