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Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
Published on: May 1, 2015
Congenital infiltrating lipomatosis
Murillo Francisco Pires Fraga1, Daniel Mello, Douglas Jorge
1Plastic Surgery Discipline of the Surgery Department, Santa Casa de São Paulo, Faculty of Medical Sciences, São Paulo, Brazil. Murifraga@ig.com.br
Journal of Plastic, Reconstructive & Aesthetic Surgery : JPRAS
|January 7, 2009
Summary
Congenital infiltrating lipomatosis (LCI) is a rare soft-tissue neoplasm characterized by fat infiltration and bone hypertrophy. This case report details facial LCI in a child, discussing diagnosis and treatment strategies.
Area of Science:
- Pathology
- Oncology
- Pediatrics
Background:
- Congenital infiltrating lipomatosis (LCI) is a rare, benign soft-tissue neoplasm.
- Characterized by mature adipocytes infiltrating surrounding tissues, nerves, and vessels.
- Often presents with adjacent bone hypertrophy, distinguishing it from other lipomatous tumors.
Observation:
- This article presents a rare case of congenital infiltrating lipomatosis affecting the face of a child.
- The clinical presentation and pathological features of facial LCI are described.
- Diagnostic challenges and therapeutic approaches for this condition are discussed.
Findings:
- LCI is defined by non-encapsulated mature adipocytes with infiltration into muscles and soft tissues.
- Key features include absence of malignancy, lipoblasts, and presence of fibrous elements.
- Observed bone hypertrophy in adjacent structures is a significant characteristic.
Implications:
- Accurate diagnosis of LCI is crucial to differentiate it from malignant liposarcomas.
- Understanding LCI's infiltrative nature guides surgical and therapeutic planning.
- This case contributes to the limited literature on pediatric facial LCI, aiding future management.
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