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AI Summary & Key Takeaways
AI Insight⚡ TL;DR(Too Long; Didn't Read)
The diagnosis can be made by ultrasonographic and magnetic resonance imaging findings for those obviating diagnostic biopsy.
📌 3 Key Takeaways
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Objective & Hypothesis:Lipofibromatous hamartoma is a rare, slow-growing, benign, fibrofatty tumor-like condition.
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Key Findings & Data:The upper extremity nerves are commonly involved.
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Conclusion & Impact:The diagnosis can be made by ultrasonographic and magnetic resonance imaging findings for those obviating diagnostic biopsy.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters
Abstract
Lipofibromatous hamartoma is a rare, slow-growing, benign, fibrofatty tumor-like condition. The upper extremity nerves are commonly involved. It is characterized by thickened axonal bundles with epineural and perineural fibrosis and fatty infiltration around the axonal bundles. Macrodactyly is a characteristic symptom in one-third of cases. Treatment options are differentiated according to the symptomatology. The diagnosis can be made by ultrasonographic and magnetic resonance imaging findings for those obviating diagnostic biopsy.
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Cite This Article
ÇOŞKUN, A., KARAMAN, Z. F., KARAMAN, İ. (2022). Lipofibromatous Hamartoma of the Upper Extremity: Report ofTwo Cases. European Archives of Medical Research, Cilt: 37 - Sayı: 2, 121–123. https://ajindex.com/articles/510304