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Case Reports
. 2022 Jul 5:80:104061.
doi: 10.1016/j.amsu.2022.104061. eCollection 2022 Aug.

Case report: Recurrent parosteal lipoma at Dr. Moewardi hospital

Affiliations
Case Reports

Case report: Recurrent parosteal lipoma at Dr. Moewardi hospital

Widyanti Soewoto et al. Ann Med Surg (Lond). .

Abstract

Background: Parosteal lipoma is a rare and benign neoplasm originating from mature adipose tissue near the periosteum. Clinically, it is difficult to diagnose due to its similarity to the clinical manifestation of sarcoma, so imaging, histopathology, and immunohistochemistry examinations are necessary.

Case presentation: A 54-year-old woman presented with lump on the right thigh that had gone through surgery eight years prior, with a diameter of 20 cm, with a partly hard and partly soft consistency, the patient was diagnosed with suspected recurrent liposarcoma. We performed wide excision and histopathological results showed a proliferation of bone cells and cartilage cells that were lobulated, surrounded by a proliferation of fat cells with no pleomorphism or immature cells.

Discussion: Parosteal lipomas are neoplasms derived from adult adipose tissue, usually connected to the periosteum, and rare and benign. Two theories of pathogenesis of parosteal lipomas. (1) tumors arise from the differentiation of stem cells derived from adipose tissue, (2) the tumor is derived from secondary metaplasia of fibroblasts due to recurrent trauma, metabolic changes, or ischemia. Based on the theory, it is likely that in this case is due to the presence of differentiation of adiposa tissue due to the non-acquisition of a history of trauma.

Conclusion: Parosteal lipoma is a rare case of benign neoplasm, which is difficult to diagnose clinically due to its similar sarcoma, thus requiring imaging and histopathological examination. The treatment of choice is wide excision by taking the entire tumor to prevent a recurrence.

Keywords: Case report; Parosteal lipoma; Rare cases; Relapsed.

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Conflict of interest statement

The authors declare no potential conflicts of interest.

Figures

Fig. 1
Fig. 1
MSCT with contrast 15–46 HU, one-third proximal – one-third distal of the femur region.
Fig. 2
Fig. 2
Macroscopic picture of a tumor divided into two encapsulated parts located intramuscularly. A. Hard mass suggesting an osteochondroma and B. Soft mass suggesting a lipoma.
Fig. 3
Fig. 3
Histopathology A. Components of chondroid, osteoid matrix, and lipoma with a 40× magnification. B Components of osteoid C. Components of lipoma with a 100× magnification. D Components of chondroid with a 400× magnification.
Fig. 4
Fig. 4
Immunohistochemistry. A. SMA with a magnification of 40. B. Vimentin with a magnification of 100. C. S100 with a magnification of 100. D. HMB-45 with a magnification of 100.

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