Frontiers in Oncology (Jul 2024)

Case report: Atypical lipomatous tumor of the thigh in a four-year-old girl

  • Itaru Ogawa,
  • Michiyuki Hakozaki,
  • Michiyuki Hakozaki,
  • Yoichi Kaneuchi,
  • Takeo Suzuki,
  • Takuya Nikaido,
  • Shoki Yamada,
  • Akihito Utsumi,
  • Osamu Hasegawa,
  • Hideki Sano,
  • Yoshihiro Matsumoto

DOI
https://doi.org/10.3389/fonc.2024.1401861
Journal volume & issue
Vol. 14

Abstract

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Atypical lipomatous tumors (ALTs) are locally aggressive adipocytic malignancies that frequently occur in middle-aged adults. We report the rare case of an ALT of the thigh that occurred in a 4-year-old girl. Since the tumor was initially diagnosed as a lipoblastoma by incisional biopsy, marginal resection was performed. Histopathological findings of the surgical specimen revealed the proliferation of mature and variously sized adipocytes, as well as ectopic ossification; these features differ from the typical findings of lipoblastoma. Immunohistochemical findings showed nuclear positivity for a murine double minute 2 (MDM2) and cyclin-dependent kinase 4 (CDK4) and negativity for pleomorphic adenoma gene 1 (PLAG1). Fluorescence in situ hybridization showed abnormal amplification of the MDM2 gene. The patient was thus finally diagnosed as having an ALT. No signs of local recurrence or metastasis were noted 1 year postoperatively. This case is instructive in the differential diagnosis of primary adipocytic tumors. Lipoblastomas are the most common adipocytic tumors in children, but if a tumor is located in the deep tissue or imaging findings are not typical, the possibility of ALT should be considered and immunohistochemistry for MDM2 and CDK4 should be added.

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