Background: Hemangiomas are benign endothelial cell-derived tumors that are present in 1-2% of newborns. They are most frequent in females. Eighty per cent are located in the head and neck region. Intramuscular hemangiomas represent 0.8% of all cases. They are characterized by rapid endothelial growth. Treatment is indicated for lesions that have an organic or visceral location or those that present with deformities.
Methods: Six cases of intramuscular hemangioma are presented. They were collected during the period June 2003 to November 2005 from all surgical cases seen at the Department of Cardiovascular Surgery, Hospital General "Dr Manuel Gea Gonzalez," Mexico City, Mexico. Their clinical appearance, treatment, and outcomes are discussed.
Results: There were five women and one man with a mean age of 24.6 years (15-44 years). Two hemangiomas were located on the upper extremities and four on the lower extremities. All six patients were treated by surgical resection. Four cavernous hemangiomas were revealed during microscopic examination. At 1-3 years of follow-up, there were no recurrences and the functional and aesthetic results were good.
Conclusions: Intramuscular hemangiomas are rare. Lesions of the extremities are even rarer. Surgical excision in the six cases described here resulted in cure with good functional and cosmetic outcomes.
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http://dx.doi.org/10.1111/j.1365-4632.2008.04033.x | DOI Listing |
J Am Acad Dermatol
January 2025
Division of Dermatology, Department of Medicine, University of Toronto, Toronto, ON, Canada; Division of Dermatology, The Hospital for Sick Children, Toronto, ON, Canada.
JACC Case Rep
December 2024
Texas Children's Hospital, Baylor College of Medicine, Houston, Texas, USA.
Fetal and neonatal cardiac tumors are rare and often benign. Clinical presentation is primarily related to mass effect, pericardial effusion or arrhythmia. Prenatal detection can assist with risk assessment and inform optimal delivery plan and postnatal management.
View Article and Find Full Text PDFJACC Case Rep
December 2024
Department of Cardiovascular Surgery, The Mount Sinai Hospital, New York, New York, USA.
A hemangioma of the mitral valve and aortomitral curtain was incidentally discovered in an adolescent. The lesion was surgically excised, and the mitral valve was reconstructed with complete preservation of valvular function. Pertinent principles of multimodality imaging-based diagnosis and nuances of operative management of this rare, vascular tumor are discussed.
View Article and Find Full Text PDFJACC Case Rep
December 2024
Icahn School of Medicine at Mount Sinai, Mount Sinai Kravis Children's Hospital, New York, New York, USA.
A 7-week-old infant with a 1-week history of a SARS-CoV2 respiratory infection presented with tachypnea. Cardiomegaly was noted on chest roentgenogram. Echocardiogram showed a large pericardial effusion, with tamponade physiology and a large pericardial mass.
View Article and Find Full Text PDFJACC Case Rep
December 2024
Department of Cardiology, Medipol University Faculty of Medicine, Istanbul, Turkey.
Cardiac hemangiomas are exceedingly rare, comprising only 5% to 10% of benign cardiac tumors. We report a patient with a large right atrial mass and end-stage heart failure with severe left ventricular dysfunction. Echocardiography revealed a mass obstructing tricuspid inflow.
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