Soewoto Widyanti, Waskita Brian, Imamsoedjana Amriansyah Pranowo
Surgical Oncology Subdivision, Dr. Moewardi Hospital, Faculty of Medicine, Sebelas Maret University, Jalan Slamet Riyadi 419 Makamhaji Kartasura Sukoharjo Jawa Tengah Indonesia, 57161, Indonesia.
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.
Ann Med Surg (Lond). 2022 Jul 5;80:104061. doi: 10.1016/j.amsu.2022.104061. eCollection 2022 Aug.
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.
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.
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.
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.
骨旁脂肪瘤是一种罕见的良性肿瘤,起源于骨膜附近的成熟脂肪组织。临床上,由于其临床表现与肉瘤相似,难以诊断,因此需要进行影像学、组织病理学和免疫组织化学检查。
一名54岁女性,右大腿出现肿块,8年前曾接受过手术,肿块直径20厘米,质地软硬不均,患者被诊断为疑似复发性脂肪肉瘤。我们进行了广泛切除,组织病理学结果显示骨细胞和软骨细胞呈分叶状增生,周围有脂肪细胞增生,无多形性或未成熟细胞。
骨旁脂肪瘤是一种起源于成人脂肪组织的肿瘤,通常与骨膜相连,罕见且为良性。骨旁脂肪瘤的发病机制有两种理论。(1)肿瘤起源于脂肪组织来源的干细胞分化,(2)肿瘤是由于反复创伤、代谢变化或缺血导致成纤维细胞继发性化生而来。基于该理论,在本病例中,可能是由于未获取创伤史而存在脂肪组织分化。
骨旁脂肪瘤是一种罕见的良性肿瘤,由于其与肉瘤相似,临床上难以诊断,因此需要进行影像学和组织病理学检查。首选的治疗方法是广泛切除整个肿瘤以防止复发。