5
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Case report: Recurrent parosteal lipoma at Dr. Moewardi hospital

      case-report

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          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.

          Highlights

          • 45 year old woman with recurrent parosteal lipoma.

          • The case of parosteal lipoma is a benign tumor.

          • A neoplasm originating from mature adipose tissue, mostly located in the bone cortex below the periosteum.

          • The incidence is 0.3% of all types of lipomas and 0.1% of primary bone neoplasms.

          Related collections

          Most cited references15

          • Record: found
          • Abstract: found
          • Article: not found

          The SCARE 2020 Guideline: Updating Consensus Surgical CAse REport (SCARE) Guidelines

          The SCARE Guidelines were first published in 2016 and were last updated in 2018. They provide a structure for reporting surgical case reports and are used and endorsed by authors, journal editors and reviewers, in order to increase robustness and transparency in reporting surgical cases. They must be kept up to date in order to drive forwards reporting quality. As such, we have updated these guidelines via a DELPHI consensus exercise.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Well-circumscribed deep-seated lipomas of the upper extremity. A report of 13 cases

              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Osteochondrolipoma of the submandibular region: a case report and review of the literature.

              Lipoma is an extremely common and ubiquitous benign soft tissue tumor composed of mature adipose tissue, with frequent differentiation towards other mesenchymal elements such as blood vessels, fibrous tissue, or muscle. They are typically slow-growing, encapsulated, superficial or deep, and have a wide range in size depending on their location. The presence of cartilage or bone is very rare, with most reported cases in the head and neck area. We report the case of an osteochondrolipoma of the submandibular region with associated benign bone marrow elements, with a review of the literature and discussion of the differential diagnosis.
                Bookmark

                Author and article information

                Contributors
                Journal
                Ann Med Surg (Lond)
                Ann Med Surg (Lond)
                Annals of Medicine and Surgery
                Elsevier
                2049-0801
                05 July 2022
                August 2022
                05 July 2022
                : 80
                : 104061
                Affiliations
                [a ]Surgical Oncology Subdivision, Dr. Moewardi Hospital, Faculty of Medicine, Sebelas Maret University, Jalan Slamet Riyadi 419 Makamhaji Kartasura Sukoharjo Jawa Tengah Indonesia, 57161, Indonesia
                [b ]Pathology Anatomy Department, Dr. Moewardi Hospital, Faculty of Medicine, Sebelas Maret University, Bagian Patologi Anatomi RS Dr Moewardi Surakarta. Jalan Kol. Sutarto 132 Jebres Surakarta Jawa Tengah Indonesia, 57126, Indonesia
                [c ]Department of Surgery, Faculty of Medicine, Sebelas Maret University, Bagian Bedah RS Dr Moewardi Surakarta. Jalan Kol. Sutarto 132 Jebres Surakarta Jawa Tengah Indonesia, 57126, Indonesia
                Author notes
                []Corresponding author. widyanti_s@ 123456staff.uns.ac.id
                Article
                S2049-0801(22)00821-4 104061
                10.1016/j.amsu.2022.104061
                9283799
                35846859
                e1871716-53b0-47a4-b6e2-abe2a6dd5cd3
                © 2022 The Author(s)

                This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).

                History
                : 29 April 2022
                : 19 June 2022
                : 22 June 2022
                Categories
                Case Report

                case report,rare cases,parosteal lipoma,relapsed
                case report, rare cases, parosteal lipoma, relapsed

                Comments

                Comment on this article