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1000 Titel
  • A large retroperitoneal lipoblastoma as an incidental finding: a case report
1000 Autor/in
  1. Gerhard-Hartmann, Elena |
  2. Wiegering, Verena |
  3. Benoit, Clemens |
  4. Meyer, Thomas |
  5. Rosenwald, Andreas |
  6. Maurus, Katja |
  7. Ernestus, Karen |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-04
1000 Erschienen in
1000 Quellenangabe
  • 21(1):159
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12887-021-02628-w |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8019505/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Background!#!Lipoblastoma is a rare benign mesenchymal neoplasm of infancy that most commonly occurs on the extremities and trunk but can arise at variable sites of the body. Retroperitoneal lipoblastomas are particularly rare but can grow to enormous size, and preoperative diagnosis is difficult with diverse, mostly malignant differential diagnoses that would lead to aggressive therapy. Since lipoblastoma is a benign tumor that has an excellent prognosis after resection, correct diagnosis is crucial.!##!Case presentation!#!A case of a large retroperitoneal tumor of a 24-month old infant that was clinically suspicious of a malignant tumor is presented. Due to proximity to the right kidney, clinically most probably a nephroblastoma or clear cell sarcoma of the kidney was suspected. Radiological findings were ambiguous. Therefore, the mass was biopsied, and histology revealed an adipocytic lesion. Although mostly composed of mature adipocytes, in view of the age of the patient, the differential diagnosis of a (maturing) lipoblastoma was raised, which was supported by molecular analysis demonstrating a HAS2-PLAG1 fusion. The tumor was completely resected, and further histopathological workup led to the final diagnosis of a 13 cm large retroperitoneal maturing lipoblastoma. The child recovered promptly from surgery and showed no evidence of recurrence so far.!##!Conclusion!#!Although rare, lipoblastoma should be included in the differential diagnoses of retroperitoneal tumors in infants and children, and molecular diagnostic approaches could be a helpful diagnostic adjunct in challenging cases.
1000 Sacherschließung
lokal General pediatric medicine and surgery
lokal Lipoblastoma
lokal Humans [MeSH]
lokal Case report
lokal Retroperitoneal tumor
lokal Diagnosis, Differential [MeSH]
lokal Infant [MeSH]
lokal Lipoblastoma/diagnosis [MeSH]
lokal Lipoblastoma/surgery [MeSH]
lokal Prognosis [MeSH]
lokal Neoplasm Recurrence, Local [MeSH]
lokal Child [MeSH]
lokal Pediatric
lokal Transcription Factors [MeSH]
lokal Case Report
lokal Child, Preschool [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0003-2134-2774|https://frl.publisso.de/adhoc/uri/V2llZ2VyaW5nLCBWZXJlbmE=|https://frl.publisso.de/adhoc/uri/QmVub2l0LCBDbGVtZW5z|https://frl.publisso.de/adhoc/uri/TWV5ZXIsIFRob21hcw==|https://frl.publisso.de/adhoc/uri/Um9zZW53YWxkLCBBbmRyZWFz|https://frl.publisso.de/adhoc/uri/TWF1cnVzLCBLYXRqYQ==|https://frl.publisso.de/adhoc/uri/RXJuZXN0dXMsIEthcmVu
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1000 Erstellt am 2023-11-15T12:25:19.123+0100
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