Glomangiosarcoma: Difference between revisions
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{{Infobox medical condition | |||
| name = Glomangiosarcoma | |||
| synonyms = Malignant glomus tumor | |||
| field = [[Oncology]], [[Dermatology]] | |||
| symptoms = [[Pain]], [[swelling]], [[tenderness]] | |||
| complications = [[Metastasis]] | |||
| onset = Typically in [[adulthood]] | |||
| duration = [[Chronic]] | |||
| types = | |||
| causes = Unknown, possibly [[genetic mutations]] | |||
| risks = Previous [[glomus tumor]], [[genetic predisposition]] | |||
| diagnosis = [[Biopsy]], [[imaging studies]] | |||
| differential = [[Benign glomus tumor]], [[hemangiopericytoma]], [[leiomyosarcoma]] | |||
| prevention = None known | |||
| treatment = [[Surgical excision]], [[radiation therapy]], [[chemotherapy]] | |||
| medication = | |||
| prognosis = Variable, depends on stage and metastasis | |||
| frequency = Rare | |||
}} | |||
'''Glomangiosarcoma''' is a rare type of [[tumor]] that originates from the [[glomus body]], a type of [[nerve]] tissue found throughout the body. This type of tumor is a malignant (cancerous) form of a [[glomus tumor]], which is typically benign (non-cancerous). | '''Glomangiosarcoma''' is a rare type of [[tumor]] that originates from the [[glomus body]], a type of [[nerve]] tissue found throughout the body. This type of tumor is a malignant (cancerous) form of a [[glomus tumor]], which is typically benign (non-cancerous). | ||
== Symptoms == | == Symptoms == | ||
The symptoms of glomangiosarcoma can vary depending on the location of the tumor. Common symptoms may include [[pain]], sensitivity to temperature changes, and a noticeable mass or lump. In some cases, the tumor may cause functional impairment if it compresses nearby structures or nerves. | The symptoms of glomangiosarcoma can vary depending on the location of the tumor. Common symptoms may include [[pain]], sensitivity to temperature changes, and a noticeable mass or lump. In some cases, the tumor may cause functional impairment if it compresses nearby structures or nerves. | ||
== Causes == | == Causes == | ||
The exact cause of glomangiosarcoma is unknown. It is thought to arise from the cells of the glomus body, which are involved in regulating body temperature. These tumors are not typically associated with any inherited syndromes or environmental exposures. | The exact cause of glomangiosarcoma is unknown. It is thought to arise from the cells of the glomus body, which are involved in regulating body temperature. These tumors are not typically associated with any inherited syndromes or environmental exposures. | ||
== Diagnosis == | == Diagnosis == | ||
Diagnosis of glomangiosarcoma typically involves a combination of [[physical examination]], imaging studies such as [[MRI]] or [[CT scan]], and [[biopsy]] of the tumor. The diagnosis is confirmed by a [[pathologist]] who examines the biopsy under a microscope. | Diagnosis of glomangiosarcoma typically involves a combination of [[physical examination]], imaging studies such as [[MRI]] or [[CT scan]], and [[biopsy]] of the tumor. The diagnosis is confirmed by a [[pathologist]] who examines the biopsy under a microscope. | ||
== Treatment == | == Treatment == | ||
Treatment for glomangiosarcoma typically involves [[surgery]] to remove the tumor. In some cases, [[radiation therapy]] or [[chemotherapy]] may be used in addition to surgery, particularly if the tumor is large or has spread to other parts of the body. | Treatment for glomangiosarcoma typically involves [[surgery]] to remove the tumor. In some cases, [[radiation therapy]] or [[chemotherapy]] may be used in addition to surgery, particularly if the tumor is large or has spread to other parts of the body. | ||
== Prognosis == | == Prognosis == | ||
The prognosis for glomangiosarcoma varies depending on the size and location of the tumor, as well as the patient's overall health. In general, these tumors are considered to be aggressive and have a high risk of recurrence and metastasis. | The prognosis for glomangiosarcoma varies depending on the size and location of the tumor, as well as the patient's overall health. In general, these tumors are considered to be aggressive and have a high risk of recurrence and metastasis. | ||
== See also == | == See also == | ||
* [[Glomus tumor]] | * [[Glomus tumor]] | ||
* [[Sarcoma]] | * [[Sarcoma]] | ||
* [[Cancer]] | * [[Cancer]] | ||
[[Category:Rare diseases]] | [[Category:Rare diseases]] | ||
[[Category:Cancers]] | [[Category:Cancers]] | ||
[[Category:Tumors]] | [[Category:Tumors]] | ||
{{stub}} | {{stub}} | ||
{{No image}} | {{No image}} | ||
Latest revision as of 01:04, 4 April 2025
| Glomangiosarcoma | |
|---|---|
| Synonyms | Malignant glomus tumor |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Pain, swelling, tenderness |
| Complications | Metastasis |
| Onset | Typically in adulthood |
| Duration | Chronic |
| Types | |
| Causes | Unknown, possibly genetic mutations |
| Risks | Previous glomus tumor, genetic predisposition |
| Diagnosis | Biopsy, imaging studies |
| Differential diagnosis | Benign glomus tumor, hemangiopericytoma, leiomyosarcoma |
| Prevention | None known |
| Treatment | Surgical excision, radiation therapy, chemotherapy |
| Medication | |
| Prognosis | Variable, depends on stage and metastasis |
| Frequency | Rare |
| Deaths | N/A |
Glomangiosarcoma is a rare type of tumor that originates from the glomus body, a type of nerve tissue found throughout the body. This type of tumor is a malignant (cancerous) form of a glomus tumor, which is typically benign (non-cancerous).
Symptoms[edit]
The symptoms of glomangiosarcoma can vary depending on the location of the tumor. Common symptoms may include pain, sensitivity to temperature changes, and a noticeable mass or lump. In some cases, the tumor may cause functional impairment if it compresses nearby structures or nerves.
Causes[edit]
The exact cause of glomangiosarcoma is unknown. It is thought to arise from the cells of the glomus body, which are involved in regulating body temperature. These tumors are not typically associated with any inherited syndromes or environmental exposures.
Diagnosis[edit]
Diagnosis of glomangiosarcoma typically involves a combination of physical examination, imaging studies such as MRI or CT scan, and biopsy of the tumor. The diagnosis is confirmed by a pathologist who examines the biopsy under a microscope.
Treatment[edit]
Treatment for glomangiosarcoma typically involves surgery to remove the tumor. In some cases, radiation therapy or chemotherapy may be used in addition to surgery, particularly if the tumor is large or has spread to other parts of the body.
Prognosis[edit]
The prognosis for glomangiosarcoma varies depending on the size and location of the tumor, as well as the patient's overall health. In general, these tumors are considered to be aggressive and have a high risk of recurrence and metastasis.
