Background: Intramuscular myxoma is a rare benign soft tissue tumour of mesenchymal origin, which appears as a painless mass of slow growth. Early diagnosis is important in order to differentiate it from other entities, especially soft tissue sarcoma.
Clinical Cases: Two cases, both women with a mean age of 52.5 years (range 40-65) are presented. The first was seen due to growth of a gluteal mass, and the second by coccydynia. Computed tomography and nuclear magnetic resonance were the diagnostic tests of choice. In one case, where there was a single but large lesion, radical extirpation of the gluteal muscle was chosen. In the other case, in which the lesions were multiple, individualised excision of cysts was performed. Postoperative functional limitation was low in both types of surgery, with good oncological results being obtained.
Conclusion: Intramuscular myxomas are benign lesions. There are no cases of malignancy or recurrence due to incomplete resection. It has to be determined whether they are single or multiple, since in the latter case, they could be due to syndromes such as Mazabraud syndrome, which is associated with bone fibrous dysplasia, or Albright syndrome that is also associated with pigmented skin spots.
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http://dx.doi.org/10.1016/j.circir.2016.05.003 | DOI Listing |
Med Ultrason
December 2024
Department of Medical Ultrasound, Yanbian University Hospital,Yanji, Jilin, China.
Plast Reconstr Surg Glob Open
December 2024
From the Plastic and Reconstructive Surgery Department, Hamad Medical Corporation, Doha, Qatar.
Intramuscular myxoma (IM) is a rare benign soft-tissue neoplasm that most commonly involves the thigh muscles. It presents as a painless, solitary, slow-growing mass. The definitive diagnosis of IM can only be made by histopathological examination of the lesion.
View Article and Find Full Text PDFInt J Surg Case Rep
December 2024
American British Cowdray Medical Center, 154 Carlos Graef Fernandez Av, Central Tower, medical office 515, Mexico City 05300, Mexico.
Introduction And Importance: Mazabraud's syndrome is a rare condition, describing the presence of fibrous bone dysplasia and intramuscular myxomas, with an incidence of 1:1,000,000. The aim of this article is to provide a review of the clinical presentation of Mazabraud's syndrome, including indications for surgical treatment, and follow-up strategies.
Case Presentation: A 46-year-old woman presented with a 3-month history of a painless mass in the right gluteal region, she referred a rapid increase in the mass's volume in the 3 weeks prior to consultation.
Skeletal Radiol
October 2024
Department of Orthopedic and Trauma Surgery, Cliniques Universitaires Saint Luc, Université Catholique de Louvain (UCLouvain), Hippocrate Avenue 10, B-1200, Brussels, Belgium.
Cureus
August 2024
Department of Radiodiagnosis, Jawaharlal Nehru Medical College, Datta Meghe Institute of Higher Education and Research, Wardha, IND.
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