Department of Ophthalmology, Wills Eye Hospital, Thomas Jefferson University.
Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Perelman School of Medicine.
Ophthalmic Plast Reconstr Surg. 2019 May/Jun;35(3):e76-e80. doi: 10.1097/IOP.0000000000001378.
Atypical lipomatous tumor/well-differentiated liposarcoma is a common neoplasm of the superficial and deep soft tissues of the extremities, trunk, and retroperitoneum. Atypical lipomatous tumor/well-differentiated liposarcoma is very rare in the orbit, with only 19 previously reported cases. The authors describe a 22-year-old woman who presented with an 8-month history of diplopia and was found to have an orbital mass on MRI. The excised tumor initially was interpreted as spindle cell/pleomorphic lipoma based on its morphologic and immunohistochemical features. Nine years later, the patient returned with a recurrence that required surgical debulking. Histopathologic and molecular cytogenetic evaluation of both primary and recurrent lesions disclosed Atypical lipomatous tumor/well-differentiated liposarcoma. This case highlights the diagnostic challenges and the importance of molecular genetic studies in evaluation of fatty orbital tumors.
非典型性脂肪肉瘤/高分化脂肪肉瘤是一种常见的发生于四肢、躯干和腹膜后表浅和深部软组织的肿瘤。非典型性脂肪肉瘤/高分化脂肪肉瘤在眼眶中非常罕见,仅有 19 例先前报道。作者描述了一位 22 岁的女性,她因复视就诊,MRI 显示眼眶内有一肿块。切除的肿瘤最初根据其形态学和免疫组化特征被诊断为梭形细胞/多形性脂肪瘤。9 年后,患者因复发需要手术切除。对原发和复发病变的组织病理学和分子细胞遗传学评估显示为非典型性脂肪肉瘤/高分化脂肪肉瘤。该病例强调了在评估脂肪性眼眶肿瘤时,诊断的挑战和分子遗传学研究的重要性。