2004
DOI: 10.1016/j.jpedsurg.2004.05.029
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Chest wall lipoblastoma in a seven-month-old girl: A case report

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Cited by 14 publications
(9 citation statements)
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“…In all of the previously reported cases of lipoblastoma, operative surgery and complete tumor excision has been performed with a clear plane of dissection from surrounding tissues. 3 , 4 , 8 This was also true in our case, in which the tumor was easily detached from surrounding pericardium and pleura. The reported tumor size has been between 2 to 21 cm, 12 so our case was considered huge with a greatest diameter of 20 cm which has caused compression symptoms on heart and lung.…”
Section: Discussionsupporting
confidence: 77%
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“…In all of the previously reported cases of lipoblastoma, operative surgery and complete tumor excision has been performed with a clear plane of dissection from surrounding tissues. 3 , 4 , 8 This was also true in our case, in which the tumor was easily detached from surrounding pericardium and pleura. The reported tumor size has been between 2 to 21 cm, 12 so our case was considered huge with a greatest diameter of 20 cm which has caused compression symptoms on heart and lung.…”
Section: Discussionsupporting
confidence: 77%
“…1 It is somehow similar to myxoid liposarcoma, but it differs by the absence of pleomorphism, atypia and hyperchromasia. 3 …”
Section: Discussionmentioning
confidence: 99%
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“…Most authors recommend complete excision in a conservative fashion, with preservation of the vital structures. 1,2,4,6,7,10,13,14 Overall, the prognosis for cervical lipoblastoma is very good after complete excision. At our patient's 5-month postoperative visit, no recurrence or complications were noted.…”
Section: Discussionmentioning
confidence: 99%
“…Despite the lesions being benign, great difficulty can be encountered in its management because of its tendency to invade the different fascial planes [ 9 ]. Lipoblastoma is a tumour with good prognosis despite its potential for local invasion and rapid growth but they do not metastasize [ 10 ]. Ultrasound, magnetic resonance imaging, fine needle aspiration, and cytogenetics are important diagnostic tools for this rare tumour [ 11 ].…”
Section: Introductionmentioning
confidence: 99%