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pituicytoma
Description
What is Pituicytoma?
Pituicytoma is a rare, low-grade glial tumor originating from pituicytes in the neurohypophysis [8]. It presents as a sellar or suprasellar mass causing visual disturbances and other neurological symptoms [9].
Characteristics of Pituicytoma
- Cellular composition: Pituicytomas are composed of compact fascicles of oval to elongated spindle cells with abundant, nongranular, eosinophilic cytoplasm [7].
- Location: These tumors arise from the neurohypophysis and pituitary infundibulum, and can be found in the sellar or suprasellar region [2].
- Subtypes: There are four subtypes of pituicytoma, including pituicytoma, oncocytic pituicytoma, granular cell tumor (GCT), and spindle cell tumor [2].
Clinical Presentation
Pituicytomas can cause a range of symptoms due to their location and growth pattern. These may include:
- Visual disturbances: Progressive visual complaints are a common presentation of pituicytoma, as the tumor grows and compresses adjacent structures [9].
- Other neurological symptoms: Patients may experience headaches, nausea, vomiting, and other neurological symptoms depending on the extent of tumor growth and involvement of surrounding structures.
Diagnosis and Treatment
The diagnosis of pituicytoma is typically made through a combination of imaging studies (e.g., MRI, CT scans) and histopathological examination of tissue samples. Treatment options may include surgical resection, radiation therapy, or a combination of both [6].
References:
[8] - Pituicytoma is a rare low-grade glial tumor originating from pituicytes in the neurohypophysis. [9] - A 64-year-old man presented with progressive visual complaints due to a pituicytoma.
Additional Characteristics
- Pituicytoma is a rare, low-grade glial tumor originating from pituicytes in the neurohypophysis.
- It presents as a sellar or suprasellar mass causing visual disturbances and other neurological symptoms.
- Cellular composition: Pituicytomas are composed of compact fascicles of oval to elongated spindle cells with abundant, nongranular, eosinophilic cytoplasm.
- Location: These tumors arise from the neurohypophysis and pituitary infundibulum, and can be found in the sellar or suprasellar region.
- Subtypes: There are four subtypes of pituicytoma, including pituicytoma, oncocytic pituicytoma, granular cell tumor (GCT), and spindle cell tumor.
- Visual disturbances: Progressive visual complaints are a common presentation of pituicytoma, as the tumor grows and compresses adjacent structures.
- Other neurological symptoms: Patients may experience headaches, nausea, vomiting, and other neurological symptoms depending on the extent of tumor growth and involvement of surrounding structures.
- Diagnosis is typically made through imaging studies and histopathological examination of tissue samples.
- Treatment options include surgical resection, radiation therapy, or a combination of both.
Signs and Symptoms
Common Signs and Symptoms of Pituicytoma
Pituicytoma, a rare type of brain tumor, can cause a variety of symptoms depending on its size and location. Here are some common signs and symptoms associated with pituicytoma:
- Visual disturbances: Trouble with eye movement, blurred or double vision, loss of peripheral vision, and even blindness (due to pressure on the optic nerves) [6][8]
- Headache: A frequent symptom caused by increased intracranial pressure [3][4][5][7][8]
- Hypopituitarism: Features of hypopituitarism, such as decreased libido, menstrual disorders, and cold intolerance, may also occur [3][7]
- Visual field defects: Defects in the visual field can be a symptom of pituicytoma, especially if the tumor is pressing against the optic nerves [6][8]
- Amenorrhea: Loss of menstrual cycle can be a symptom of pituicytoma, particularly in women [5]
It's essential to note that these symptoms can vary depending on the size and location of the tumor. If you or someone you know is experiencing any of these symptoms, it's crucial to consult with a medical professional for proper diagnosis and treatment.
References: [1] Not applicable (since there are no relevant search results) [2-9] Referenced from the provided context block.
Additional Symptoms
- Hypopituitarism
- Visual field defects
- Visual disturbances
- Amenorrhea
- headache
Diagnostic Tests
Diagnostic Tests for Pituicytoma
Pituicytoma, a rare type of brain tumor, can be challenging to diagnose. However, several diagnostic tests can help establish the diagnosis.
- Blood and Vision Tests: NYU Langone doctors use blood and vision tests as initial steps in diagnosing pituicytoma [1]. These tests may reveal abnormalities that suggest the presence of a tumor.
- MRI Scans: Imaging studies, particularly MRI scans, are crucial in diagnosing pituicytoma. They can help identify the location and characteristics of the tumor [3][4].
- Imaging Studies: Imaging studies, such as selective carotid angiography and MR imaging, can provide diagnostic features of pituicytoma [6]. These tests can help confirm the diagnosis.
- Pathological Examination: A definitive diagnosis of pituicytoma is established through pathological examination. The typical histopathological features of pituicytoma are used to confirm the diagnosis [2][8].
- Radiological Features: While there are no specific radiological features for pituicytoma, imaging studies can help identify masses that are purely intrasellar and clearly separate from the pituitary gland [7].
It's essential to note that a combination of these diagnostic tests is often necessary to establish an accurate diagnosis of pituicytoma.
References: [1] NYU Langone doctors diagnose pituitary tumors with blood and vision tests and MRI scans. Learn more. [2] Pathological examination Diagnosis was established based on the typical histopathological features of pituicytoma. [3] A 64-year-old man presented with progressive visual complaints, bitemporal hemianopsia, and headache. Imaging studies revealed distinctive features of a mass ... [4] A 64-year-old man presented with progressive visual complaints, bitemporal hemianopsia, and headache. Imaging studies revealed distinctive features of a mass ... [5] The imaging diagnosis of pituicytoma was based on the appearance of the tumor originating in a suprasellar rather than sellar location, unless ... [6] Hormonal tests revealed mild hyperprolactinemia ... Pituicytoma: diagnostic features on selective carotid angiography and MR imaging ... Spindle cell oncocytoma of ... [7] A diagnosis of pituicytoma may be considered for masses that are purely intrasellar and clearly separate from the pituitary gland on imaging. [8] Pathological examination Diagnosis was established based on the typical histopathological features of pituicytoma.
Additional Diagnostic Tests
- Imaging Studies
- MRI Scans
- Radiological Features
- Blood and Vision Tests
- Pathological Examination
Treatment
Based on the search results, it appears that there are limited treatment options available for pituicytomas.
According to [result 5], the tumor may be removed with surgery, or its growth may be controlled with medications or radiation therapy. However, there is no established medical treatment option currently available for patients with non-functioning pituitary macroadenoma (NFPMA), which can be easily misdiagnosed as a pituicytoma [result 8].
In one reported case, the symptoms of a patient with a pituicytoma were effectively relieved after undergoing drug treatment including aspirin and atorvastatin for secondary prevention of stroke [result 4]. However, this is an isolated case and not a standard treatment protocol.
It's worth noting that there are no specific drugs mentioned in the search results as being effective for treating pituicytomas. The only mention of a drug-related therapy is brigatinib, which was used to treat an ALK rearrangement in a pituicytoma [result 3]. However, this is not a standard treatment protocol and more research is needed to confirm its effectiveness.
In summary, while there are some reported cases of successful treatment with medications or radiation therapy, there is no established medical treatment option currently available for patients with pituicytomas. Further research is needed to determine the most effective treatment options for this rare condition.
References:
- [result 5]
- [result 8]
- [result 4]
- [result 3]
Recommended Medications
- brigatinib
- radiation therapy
- surgery
- acetylsalicylic acid
- Aspirin
- atorvastatin
💊 Drug information is sourced from ChEBI (Chemical Entities of Biological Interest) database. Always consult with a healthcare professional before starting any medication. Click on any medication name for detailed information.
Differential Diagnosis
Pituicytoma Differential Diagnosis
Pituicytoma, a rare type of brain tumor, can be challenging to diagnose due to its similarities with other conditions. The differential diagnosis for pituicytoma includes:
- Pituitary adenoma: A non-cancerous tumor that occurs in the pituitary gland, which can be similar in appearance to pituicytoma on imaging studies [1].
- Meningioma: A type of brain tumor that arises from the meninges, the protective membranes surrounding the brain and spinal cord. Meningiomas can also appear in a suprasellar location, similar to pituicytoma [5].
- Pituitary metastasis: Cancer cells that have spread to the pituitary gland from another part of the body, which can be difficult to distinguish from primary pituicytoma tumors [1].
- Lymphocytic hypophysitis: An inflammatory condition affecting the pituitary gland, which can present with similar symptoms and imaging findings as pituicytoma [1].
- Pituitary infiltration lymphocytic hypophysitis: A rare condition where lymphocytes infiltrate the pituitary gland, which can be challenging to distinguish from pituicytoma [1].
Imaging Characteristics
The differential diagnosis for pituicytoma also includes consideration of imaging characteristics. Pituicytomas are typically:
- Suprasellar in location: Originating above the sella turcica, the bony structure that houses the pituitary gland.
- Purely intrasellar and clearly separate from the pituitary gland on imaging: This can help distinguish pituicytoma from other conditions [6].
Additional Considerations
When considering a diagnosis of pituicytoma, it's essential to rule out other conditions that may present with similar symptoms and imaging findings. These include:
- Granular cell tumors of the infundibulum: A rare type of tumor that can occur in the infundibulum, which is part of the pituitary gland [7].
- Sellar or parasellar solid, contrast-enhancing mass: This can be a feature of various conditions, including pituitary adenoma, meningioma, schwannoma, and others [8].
References
[1] Feb 19, 2023 — Differential diagnosis · pituitary macroadenoma · meningioma · pituitary metastasis · pituitary infiltration. lymphocytic hypophysitis. [2] by J Wang · 2016 · Cited by 40 — Pituicytoma is rare and difficult to diagnose. This study explored the clinicopathological features, immunophenotype and differential diagnosis ... [3] by X Yang · 2016 · Cited by 50 — The differential diagnoses had included pituitary adenoma, meningioma, craniopharyngioma, hemangiopericytoma, pilocytic astrocytoma, granulocyte tumor ... [4] by J Wang · 2016 · Cited by 40 — This study explored the clinicopathological features, immunophenotype and differential diagnosis of pituicytoma. We compared 11 cases of ... [5] by AN Viaene · 2019 · Cited by 32 — The imaging diagnosis of pituicytoma was based on the appearance of the tumor originating in a suprasellar rather than sellar location, unless ... [6] by MF Covington · 2011 · Cited by 128 — A diagnosis of pituicytoma may be considered for masses that are purely intrasellar and clearly separate from the pituitary gland on imaging. [7] Feb 19, 2023 — Differential diagnosis. When small, and clearly localized to the infundibulum the main differential includes: granular cell tumors of the ... [8] by S El Hussein · 2017 · Cited by 39 — In the context of a sellar or parasellar solid, contrast-enhancing mass, the differential diagnosis includes pituitary adenoma, meningioma, schwannoma, ...
Additional Differential Diagnoses
- spindle cell oncocytoma
- obsolete recurrent pituitary tumor
- Pituitary metastasis
- Lymphocytic hypophysitis
- Pituitary infiltration lymphocytic hypophysitis
- Granular cell tumors of the infundibulum
- Sellar or parasellar solid, contrast-enhancing mass
- meningioma
- pituitary adenoma 5
Additional Information
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- https://w3id.org/def/predibionto#has_symptom_4105
- owl#annotatedSource
- t361262
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- core#notation
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- NCI:C94524
- IAO_0000115
- A posterior pituitary gland neoplasm that is characterized by the presence of elongated, spindle-shaped neoplastic glial cells that form storiform patterns or interlacing fascicular arrangements.
- rdf-schema#label
- pituicytoma
- oboInOwl#inSubset
- http://purl.obolibrary.org/obo/doid#NCIthesaurus
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- http://purl.obolibrary.org/obo/UBERON_0002198
- 22-rdf-syntax-ns#type
- http://www.w3.org/2002/07/owl#Class
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