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title, docid, authors, breadcrumbs, category, cmeTopicId, documentVersionId, imageCount, lastUpdated, pageDescription, pageKeywords, pageTitle, enhancedTitle, type, references, breadcrumbs
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| Enhancing Suprasellar Mass | 528eaea9-095f-4fab-ad42-5ad84e215a2d |
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Brain | 01b1cc14-8442-4bbd-93ff-bd8895b90f87 | 39bca65a-aa9f-4818-9b63-d727551a81f1 | 19 | 01/26/23 | Enhancing Suprasellar Mass | Brain, Differential Diagnosis, Sella/Juxtasellar, Pineal Region, Anatomically Based Differentials, Enhancing Suprasellar Mass | Enhancing Suprasellar Mass | STATdx | Enhancing Suprasellar Mass | DDX | true |
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title: "Enhancing Suprasellar Mass" docid: "528eaea9-095f-4fab-ad42-5ad84e215a2d" authors:
- key: "318f80ab-6abb-4067-a809-2ebdaa5a30c9" value: "Kalen Riley, MD, MBA"
- key: "5cff4116-3654-4b3a-bb75-5ebe0b8c9850" value: "Anne G. Osborn, MD, FACR"
- key: "8d5254e9-8dda-478b-8f08-bdee97a32c79" value: "Karen L. Salzman, MD, FACR" breadcrumbs:
- name: "Brain" slug: "brain" treeNodeId: "6d8829f1-14d7-45af-8675-255189aa526a"
- name: "Differential Diagnosis" slug: "differential-diagnosis" treeNodeId: "a7fdd139-664e-4bb8-8d18-400e4733ff60"
- name: "Sella/Juxtasellar, Pineal Region" slug: "sellajuxtasellar-pineal-region" treeNodeId: "5e38b9c1-3137-47e3-aa83-1fc82cb4099a"
- name: "Anatomically Based Differentials" slug: "anatomically-based-differentials" treeNodeId: "7a51b2ca-8fee-4c16-aff3-b7189f68ea60"
- name: "Enhancing Suprasellar Mass" slug: "enhancing-suprasellar-mass" treeNodeId: null category: "Brain" cmeTopicId: "01b1cc14-8442-4bbd-93ff-bd8895b90f87" documentVersionId: "39bca65a-aa9f-4818-9b63-d727551a81f1" imageCount: 19 lastUpdated: "01/26/23" pageDescription: "Enhancing Suprasellar Mass" pageKeywords: "Brain, Differential Diagnosis, Sella/Juxtasellar, Pineal Region, Anatomically Based Differentials, Enhancing Suprasellar Mass" pageTitle: "Enhancing Suprasellar Mass | STATdx" enhancedTitle: "Enhancing Suprasellar Mass" type: "DDX" references: true breadcrumbs:
- "Brain"
- "Differential Diagnosis"
- "Sella/Juxtasellar, Pineal Region"
- "Anatomically Based Differentials"
- "Enhancing Suprasellar Mass"
ESSENTIAL INFORMATION
-
Key Differential Diagnosis Issues
- Effect of age on differential diagnosis important
- Common lesions ("big 5") account for > 75% of all suprasellar masses
- Most other lesions < 1-2% each
- Differential diagnosis narrows if mass confined to infundibulum
-
Helpful Clues for Common Diagnoses
- Pituitary Macroadenoma vs. Meningioma - Macroadenoma: Gland cannot be identified separate from mass - Meningioma: Mass distinct from gland (diaphragma sellae separates mass above from pituitary below)
- SaccularAneurysm - Coronal plane helps distinguish aneurysm from pituitary - Look for phase artifact, flow void on MR
- Craniopharyngioma - Adamantinomatous: 90% Ca⁺⁺, 90% cystic, 90% enhance - Papillary may be solid, noncalcified, enhance strongly
- Pilocytic Astrocytoma - More common in children than adults - T2 hyperintense, variable enhancement - Expands hypothalamus, optic chiasm - May extend into optic nerves/tracts
- Pilomyxoid Astrocytoma - Subtype of pilocytic astrocytoma, more aggressive - Infant > child - Large, bulky tumor with lateral extension to temporal lobe common - Hemorrhage in 20-25%
-
Helpful Clues for Less Common Diagnoses
- Pituitary Hyperplasia - May be physiologic (pregnancy, lactation, puberty) - Pathologic in end-organ failure (thyroid, ovarian, etc.)
- Neurosarcoid - Older patients, enhancing mass
- Langerhans Cell Histiocytosis - Children and young adults; enhancing mass - May cause thickened infundibulum - Absence of pituitary "bright spot"
- Germinoma - Children > > adults; enhancing mass - CT hyperdense - May cause thickened infundibulum - Absence of the pituitary "bright spot"
- Lymphocytic Hypophysitis - Can mimic pituitary adenoma on imaging - Most common in peripartum female - May be autoimmune, inflammatory, granulomatous process, drug related - May be secondary to checkpoint inhibitor therapy
- Astrocytoma, IDH-Mutant - May affect hypothalamic and suprasellar regions - T2 hyperintense; variable enhancement - WHO grades 2-4
-
Helpful Clues for Rare Diagnoses
- Solitarymetastasis to gland &/or stalk rare
- Lymphoma, leukemia usually with systemic disease
- Pituicytoma, g****ranular cell tumor, and spindle cell oncocytoma are rare tumors, which may occur along infundibulum &/or posterior pituitary or may mimic macroadenoma
-
Alternative Differential Approaches
- Adult: Consider adenoma, meningioma, and aneurysm
- Child: Craniopharyngioma, astrocytoma, Langerhans cell histiocytosis, and germinoma
References
Selected References
- Kinoshita Y et al: Natural course of Rathke's cleft cysts and risk factors for progression. J Neurosurg. 1-7, 2022
- Pascual JM et al: Duct-like recess in the infundibular portion of third ventricle craniopharyngiomas: an MRI sign identifying the papillary type. AJNR Am J Neuroradiol. 43(9):1333-40, 2022
- Poyuran R et al: Nonneoplastic and noninfective cysts of the central nervous system: a histopathological study. Neuropathology. ePub, 2022
- Jipa A et al: Imaging of the sellar and parasellar regions. Clin Imaging. 77:254-75, 2021
- Kurokawa R et al: MRI findings of immune checkpoint inhibitor-induced hypophysitis: possible association with fibrosis. AJNR Am J Neuroradiol. 41(9):1683-9, 2020
- Go JL et al: Imaging of the sella and parasellar region. Radiol Clin North Am. 55(1):83-101, 2017
- Seeburg DP et al: Imaging of the sella and parasellar region in the pediatric population. Neuroimaging Clin N Am. 27(1):99-121, 2017
- Zamora C et al: Sellar and parasellar imaging. Neurosurgery. 80(1):17-38, 2017
- Patel KS et al: Intraoperative magnetic resonance imaging assessment of non-functioning pituitary adenomas during transsphenoidal surgery. Pituitary. 19(2):222-31, 2016
- Petrakakis I et al: The sellar and suprasellar region: a "hideaway" of rare lesions. Clinical aspects, imaging findings, surgical outcome and comparative analysis. Clin Neurol Neurosurg. 149:154-65, 2016
- Wang J et al: The clinicopathological features of pituicytoma and the differential diagnosis of sellar glioma. Neuropathology. 36(5):432-440, 2016
- Wu AW et al: Chondroid chordoma of the sella turcica mimicking a pituitary adenoma. Ear Nose Throat J. 94(10-11):E47-9, 2015
- DW Louis, et. al (Editors). WHO Classification of Tumours of the Central Nervous System. International Agency for Research on Cancer, Lyon, 2016. Chapter 17: Tumours of the sellar region, pp 323-334.
Images
Selected Images
Pituitary Macroadenoma
Coronal T1 C+ MR shows an enhancing intrasellar and suprasellar mass
. The pituitary gland cannot be separated from the mass and indeed is the mass. Note the superior displacement of the optic chiasm
by the macroadenoma.
Pituitary Macroadenoma
Coronal T1 C+ MR shows an enhancing intrasellar and suprasellar mass
. The pituitary gland cannot be separated from the mass and indeed is the mass. Note the superior displacement of the optic chiasm
by the macroadenoma.
Meningioma
Coronal T1 C+ FS MR shows a suprasellar enhancing mass
separate from the normal pituitary gland below
. Meningiomas often have associated hyperostosis of the adjacent bone. Additionally, these benign tumors enhance homogeneously and may have an associated dural tail.
Saccular Aneurysm
Axial T1 C+ MR shows a suprasellar enhancing mass
with prominent phase artifact
caused by large basilar tip aneurysm with slow intraluminal flow. Aneurysms are the 3rd most common suprasellar mass in an adult.
Craniopharyngioma
Sagittal T1 C+ MR shows an enhancing, partially solid and cystic suprasellar mass
related to an adamantinomatous craniopharyngioma. These WHO grade 1 tumors are the most common pediatric intracranial tumor of nonglial origin.
Pilomyxoid Astrocytoma
Coronal T1 C+ FS MR shows a heterogeneously enhancing suprasellar mass
in a child that was found to represent a pilomyxoid astrocytoma, WHO grade 1. Pilomyxoid astrocytoma is a subtype of pilocytic astrocytoma that is often more aggressive.
Neurosarcoid
Axial T1 C+ FS MR shows a lobular, enhancing suprasellar mass
related to neurosarcoid. Patients with neurosarcoid often have associated pulmonary hilar adenopathy.
Langerhans Cell Histiocytosis
Axial T1 C+ FS MR shows a diffusely enhancing suprasellar mass
in a young adult who first presented with diabetes insipidus and a thick, enhancing infundibulum with absence of a posterior pituitary bright spot. Nine months later, patient returned with a much larger suprasellar mass.
Lymphocytic Hypophysitis
Coronal T2 MR in a pregnant patient with acute vision problems shows a sellar and suprasellar mass
with superior displacement of the optic chiasm
. Imaging of lymphocytic hypophysitis may mimic a pituitary macroadenoma.
Additional Images
Pituitary Macroadenoma
Coronal T1 C+ MR shows an inhomogeneously enhancing intra- and suprasellar mass
; the pituitary gland cannot be found separate from it and indeed is the mass.
Meningioma
Coronal T1 C+ FS MR shows a suprasellar enhancing mass
separated from the normal pituitary gland below
by a thin black line of diaphragma sellae
.
Craniopharyngioma
Coronal T1 C+ MR in a child shows a intra-/suprasellar mass. An apical nonenhancing portion is surrounded by a thin enhancing rim
. The solid portion enhances strongly but heterogeneously
.
Craniopharyngioma
Sagittal T1 C+ FS MR shows a papillary craniopharyngioma in an adult man. Papillary craniopharyngiomas are most often solid masses.
Astrocytoma, IDH-Mutant
Coronal T1 C+ MR shows an enhancing suprasellar mass
separate from the pituitary gland below
. Note involvement of the optic chiasm
.
Pilocytic Astrocytoma
Sagittal T1 C+ MR in a 3-year-old boy with rotary nystagmus and vomiting shows a large suprasellar mass
clearly separate from the pituitary gland below
.
Neurosarcoid
Axial T1 C+ FS MR shows an enhancing suprasellar mass involving the optic chiasm
and hypothalamus
with pial enhancement along the inferior frontal lobe
. The lesion also involved the optic nerve.
Germinoma
Coronal T1 C+ FS MR in 22-year-old man with diabetes insipidus shows hydrocephalus and an enhancing sellar/suprasellar mass. Germinoma commonly presents with diabetes insipidus. A macroadenoma often has visual defects.
Rare Sellar Region Tumor (Pituicytoma, Granular Cell Tumor, Spindle Cell Oncocytoma)
Coronal T1 C+ MR shows a diffusely enhancing suprasellar mass
that involves the infundibulum. A pituicytoma was diagnosed at resection. These rare tumors are WHO grade 1 and usually arise along the infundibulum or neurohypophysis. (Courtesy A.V. Hasso, MD.)
Craniopharyngioma
Axial T1 C+ FS MR shows a cystic and solid suprasellar enhancing mass
. In an adult, craniopharyngiomas may be adamantinomatous or papillary types. Adamantinomatous craniopharyngiomas enhance, calcify, and have cysts. Papillary craniopharyngiomas are commonly solid and enhancing. These are WHO grade 1 tumors.
Pilocytic Astrocytoma
Coronal T1 C+ FS MR in 25-year-old woman with visual complaints shows an enhancing suprasellar mass
that partially encases the optic chiasm
. There is also a parasellar cystic portion
of the mass. Pilocytic astrocytomas often present as a solid and cystic cerebellar mass in a child or young adult. These WHO grade 1 tumors are typically T2 hyperintense with variable enhancement.