SavedAdd your journal

Journals / İstanbul Medical Journal / 2020 / Cilt: 21 - Sayı: 1

Intramuscular Myxoma of the Right Cruris: A Case Report

Intramuscular myxoma is one of the rare soft tissue benign tumours. The most common localisation of the myxoma is the heart muscle. It has been reported less frequently in the hip and around the shoulder, trunk, neck and cruris. We aimed to report th

Alican Barış
Esra Circi
Pages
4–5
Publication Date
2022-10-19
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

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

We aimed to report this rare case of the cruris.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Intramuscular myxoma is one of the rare soft tissue benign tumours.
📊
Key Findings & Data:The most common localisation of the myxoma is the heart muscle.
💡
Conclusion & Impact:We aimed to report this rare case of the cruris.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Intramuscular myxoma is one of the rare soft tissue benign tumours. The most common localisation of the myxoma is the heart muscle. It has been reported less frequently in the hip and around the shoulder, trunk, neck and cruris. We aimed to report this rare case of the cruris.

Özet

İntramusküler miksoma yumuşak dokunun iyi huylu nadir tümörlerinden biridir. Miksomanın tipik yerleşim yeri kalp kasıdır. Kalça, omuz çevresi, gövde, boyun ve bacakta daha az rastlanmaktadır. Bacakta görülen bu nadir olguyu bildirmeyi amaçladık.

🔖

Cite This Article

Barış, A., Circi, E. (2022). Intramuscular Myxoma of the Right Cruris: A Case Report. İstanbul Medical Journal, Cilt: 21 - Sayı: 1, 4–5. https://ajindex.com/articles/551899

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Domino JS, Weindel S, Woodrow S. Multiple paraspinal intramuscular myxomas: case report. J Neurosurg Spine 2019; 32: 491-632
  2. Custódio M, Antunes E, Alves G, Braz-Silva P. Unexpected diagnosis of an intramuscular myxoma arising from the masseter muscle. Br J Oral and Maxillofac Surg 2002; 58: 109-11
  3. Tirefort J, Kolo FC, Lädermann A. An Interesting Case of Intramuscular Myxoma with Scapular Bone Lysis. Case Rep Orthop 2017; 2017: 1690409
  4. Silver WP, Harrelson JM, Scully SP. Intramuscular myxoma: a clinicopathologic study of 17 patients. Clin Orthop Relat Res 2002: 191-7
  5. Enzinger FM. Intramuscular myxoma: a review and follow-up study of 34 cases. Am J Clin Pathol 1965; 43: 104-13
  6. Bekers EM, Eijkelenboom A, Rombout P, van Zwam P, Mol S, Ruijter E, et al. Identification of novel GNAS mutations in intramuscular myxoma using next-generation sequencing with single-molecule tagged molecular inversion probes. Diagn Pathol 2019; 14
  7. Wang W, Smitaman E, Rubenstein W, Hughes T, Huang BK. Post-biopsy MRI changes in the size and enhancement of intramuscular myxomas: A report of two cases. Clin Imaging 2018; 48: 55-61
  8. Jalan D, Jain P. Mazabraud’s Syndrome-A Diagnosis Commonly Missed. J Orthop Case Rep 2019; 9: 26-9
  9. Majoor B, van de Sande M, Appelman-Dijkstra N, Leithner A, Jutte P, Vélez R, et al. Prevalence and clinical features of Mazabraud’s syndrome: a multicentre European survey. J Bone Joint Surg Am 2019; 101: 160-8
  10. Macfarlane P, Lew W, Neuhaus S. An aggressive case of Mazabraud’s syndrome. Eur J Surg Oncol 2007; 33: 1087-9
  11. Fetsch JF, Laskin WB, Miettinen M. Superficial acral fibromyxoma: a clinicopathologic and immunohistochemical analysis of 37 cases of a distinctive soft tissue tumor with a predilection for the fingers and toes. Hum Pathol 2001; 32: 704-14.