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A rare intramuscular osteolipoma: A case report

INTRODUCTION: Lipomas are frequently presented in adults and account for almost 50% of all soft-tissue tumors. Osteolipomas are rare and usually located in the intraosseous region or adjacent to bone. It is very unusual for osteolipomas with no connection to bony structures. We report a rare intramu...

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Autores principales: Han, Jae Hwi, Choi, Sung, Sohn, Kyung-Rak, Hwang, Seong Mun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036695/
https://www.ncbi.nlm.nih.gov/pubmed/32092692
http://dx.doi.org/10.1016/j.ijscr.2020.01.023
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author Han, Jae Hwi
Choi, Sung
Sohn, Kyung-Rak
Hwang, Seong Mun
author_facet Han, Jae Hwi
Choi, Sung
Sohn, Kyung-Rak
Hwang, Seong Mun
author_sort Han, Jae Hwi
collection PubMed
description INTRODUCTION: Lipomas are frequently presented in adults and account for almost 50% of all soft-tissue tumors. Osteolipomas are rare and usually located in the intraosseous region or adjacent to bone. It is very unusual for osteolipomas with no connection to bony structures. We report a rare intramuscular osteolipoma independent of bone tissue. PRESENTATION OF CASE: We report a case of a 58-year-old man with painful and progressively enlarging mass in the right lower leg. A plain X-ray and computed tomography (CT) scans revealed a large homogeneous, low-fat density mass containing an oval shape calcification without bone connection. MRI showed a circumscribed mass in the peroneus muscle with a large calcified component. The patient underwent surgical excision of the mass. Histologically, benign osteolipoma was the final diagnosis. No recurrence was observed at six months follow-up. DISCUSSION: Lipoma is a common benign soft tissue neoplasm but osteolipoma is rare. Most cases osteolipomas are connected with bone. independent of bone tissue has been reported in very few cases. Most of them occurred in the head and neck area. The pathogenesis of osteolipoma is still not clear. Although CT and MRI are useful for differential diagnosis, care should be taken because sometimes they are indistinguishable from well-differentiated liposarcomas. Excisional biopsy is useful for definitive diagnosis. CONCLUSION: Although ossifying lipomas are very rare, it is important to keep them in mind when a lesion with adipose tissue in combination with ossification is encountered.
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spelling pubmed-70366952020-03-02 A rare intramuscular osteolipoma: A case report Han, Jae Hwi Choi, Sung Sohn, Kyung-Rak Hwang, Seong Mun Int J Surg Case Rep Article INTRODUCTION: Lipomas are frequently presented in adults and account for almost 50% of all soft-tissue tumors. Osteolipomas are rare and usually located in the intraosseous region or adjacent to bone. It is very unusual for osteolipomas with no connection to bony structures. We report a rare intramuscular osteolipoma independent of bone tissue. PRESENTATION OF CASE: We report a case of a 58-year-old man with painful and progressively enlarging mass in the right lower leg. A plain X-ray and computed tomography (CT) scans revealed a large homogeneous, low-fat density mass containing an oval shape calcification without bone connection. MRI showed a circumscribed mass in the peroneus muscle with a large calcified component. The patient underwent surgical excision of the mass. Histologically, benign osteolipoma was the final diagnosis. No recurrence was observed at six months follow-up. DISCUSSION: Lipoma is a common benign soft tissue neoplasm but osteolipoma is rare. Most cases osteolipomas are connected with bone. independent of bone tissue has been reported in very few cases. Most of them occurred in the head and neck area. The pathogenesis of osteolipoma is still not clear. Although CT and MRI are useful for differential diagnosis, care should be taken because sometimes they are indistinguishable from well-differentiated liposarcomas. Excisional biopsy is useful for definitive diagnosis. CONCLUSION: Although ossifying lipomas are very rare, it is important to keep them in mind when a lesion with adipose tissue in combination with ossification is encountered. Elsevier 2020-01-25 /pmc/articles/PMC7036695/ /pubmed/32092692 http://dx.doi.org/10.1016/j.ijscr.2020.01.023 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Han, Jae Hwi
Choi, Sung
Sohn, Kyung-Rak
Hwang, Seong Mun
A rare intramuscular osteolipoma: A case report
title A rare intramuscular osteolipoma: A case report
title_full A rare intramuscular osteolipoma: A case report
title_fullStr A rare intramuscular osteolipoma: A case report
title_full_unstemmed A rare intramuscular osteolipoma: A case report
title_short A rare intramuscular osteolipoma: A case report
title_sort rare intramuscular osteolipoma: a case report
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7036695/
https://www.ncbi.nlm.nih.gov/pubmed/32092692
http://dx.doi.org/10.1016/j.ijscr.2020.01.023
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