Eid Kevin, Mudalegundi Shwetha, Yao Melissa, Eid Alen, Szarko Matthew, Nguyen John
Oakland University William Beaumont School of Medicine, Rochester, MI, USA.
John A. Moran Eye Center, University of Utah, Salt Lake City, UT, USA.
J Ophthalmic Vis Res. 2025 Sep 9;20. doi: 10.18502/jovr.v20.16421. eCollection 2025.
Leiomyosarcoma (LMS) is an aggressive tumor with a high metastatic rate that rarely metastasizes to the periocular region.
A 50-year-old male with a previous two-year history of primary stage IV LMS presented with metastatic retroperitoneal LMS, which was initially incorrectly described as an eyelid chalazion refractory to medical management. An excisional biopsy sent to pathology revealed metastatic retroperitoneum LMS. There was resolution of ocular irritation following biopsy, and an oncology referral was made.
This case of metastatic LMS to the eyelid mimicking a chalazion is rare, as only six other cases have been described previously. Our case contributes to this discussion by highlighting the importance of considering metastatic disease and performing a full-thickness biopsy in a patient presenting with a non-resolving eyelid chalazion. Recognizing tumor spread to the eyelid can be an important step in the diagnosis, surveillance, and management of metastatic LMS.
平滑肌肉瘤(LMS)是一种侵袭性肿瘤,转移率高,很少转移至眼周区域。
一名50岁男性,有原发性IV期LMS病史两年,出现转移性腹膜后LMS,最初被错误地描述为药物治疗无效的眼睑睑板腺囊肿。切除活检送病理显示为转移性腹膜后LMS。活检后眼部刺激症状缓解,并转诊至肿瘤科。
这种转移性LMS累及眼睑并酷似睑板腺囊肿的病例很罕见,此前仅另有6例报道。我们的病例通过强调在出现不消退的眼睑睑板腺囊肿患者中考虑转移性疾病并进行全层活检的重要性,为这一讨论做出了贡献。认识到肿瘤扩散至眼睑可能是转移性LMS诊断、监测和管理的重要一步。