Journals / Turkish Journal of Cancer / 2000 / Cilt: 30 - Sayı: 2

Hemangiopericytoma of the parotid gland: A case report

Pages
89–93
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Because of the rarity of the condition and its unusual site of origin, a case of hemangiopericytoma of the parotid gland is being reported in a 55-year-old woman.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Hemangiopericytoma is an uncommon tumor of vascular origin arising from the pericytes of Zimmerman.
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Key Findings & Data:It represents only 1% of all vasoformative tumors.
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Conclusion & Impact:Because of the rarity of the condition and its unusual site of origin, a case of hemangiopericytoma of the parotid gland is being reported in a 55-year-old woman.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Yaşlı · Parotis bezi · Hemanjiyoperisitom

Abstract

Hemangiopericytoma is an uncommon tumor of vascular origin arising from the pericytes of Zimmerman. It represents only 1% of all vasoformative tumors. Up to one fourth of all cases of hemangiopericytoma are reported from head and neck region. An origin in the parotid gland is extremely rare, with only 30 cases reported in the world literature. Because of the rarity of the condition and its unusual site of origin, a case of hemangiopericytoma of the parotid gland is being reported in a 55-year-old woman.

Özet

Hemangiopericytoma is an uncommon tumor of vascular origin arising from the pericytes of Zimmerman. It represents only 1% of all vasoformative tumors. Up to one fourth of all cases of hemangiopericytoma are reported from head and neck region. An origin in the parotid gland is extremely rare, with only 30 cases reported in the world literature. Because of the rarity of the condition and its unusual site of origin, a case of hemangiopericytoma of the parotid gland is being reported in a 55-year-old woman.

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Cite This Article

MAHESHWARI, G. K., BABOO, H. A., GOPAL, U., WADHWA, M. K., SHUKLA, H. K. (2000). Hemangiopericytoma of the parotid gland: A case report. Turkish Journal of Cancer, Cilt: 30 - Sayı: 2, 89–93. https://ajindex.com/articles/368410

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