Sosińska-Mielcarek Katarzyna, Senkus-Konefka Elzbieta, Jaskiewicz Kazimierz, Kordek Radzislaw, Jassem Jacek
Department of Oncology and Radiotherapy, Medical University of Gedansk, Gedansk, Poland.
Acta Ophthalmol Scand. 2006 Apr;84(2):259-62. doi: 10.1111/j.1600-0420.2005.00586.x.
To report a case of intraocular medulloepithelioma, an embryonal tumour with extremely rare presentation in adults.
The case of a 44-year-old man with intraocular malignant teratoid medulloepithelioma, primarily diagnosed as intraocular teratoma, is described and the literature on this subject is reviewed.
The patient presented with progressive proptosis caused by a tumour in the left eyeball. He had a 28-year history of loss of vision in the left eye. Histopathological examination of the enucleated eye demonstrated an intraocular teratoma. No adjuvant treatment was given. Six months later the patient presented with massive progression in the left orbit and intracranial invasion. Cisplatin-based chemotherapy was administered, but discontinued after two cycles due to poor tolerance and lack of response. At subsequent pathology review, a final diagnosis of malignant teratoid medulloepithelioma was made. Salvage radiotherapy (60 Gy in 30 fractions) resulted in partial response of the intracranial lesion. However, the patient died 6 months later due to intracranial tumour progression.
Medulloepithelioma should be considered in the differential diagnosis of intraocular tumours in adults, especially in the case of coexisting, long-standing ocular symptoms. In some cases this disease is very aggressive.
报告1例眼内髓上皮瘤,这是一种在成人中表现极为罕见的胚胎性肿瘤。
描述1例44岁患有眼内恶性畸胎样髓上皮瘤的男性病例,该病例最初被诊断为眼内畸胎瘤,并对该主题的文献进行综述。
患者因左眼球肿瘤出现进行性眼球突出。他有28年左眼失明病史。摘除眼球的组织病理学检查显示为眼内畸胎瘤。未给予辅助治疗。6个月后,患者左眼眶出现大量病变进展并发生颅内侵犯。给予了以顺铂为基础的化疗,但由于耐受性差和无反应,在两个周期后停药。在随后的病理复查中,最终诊断为恶性畸胎样髓上皮瘤。挽救性放疗(30次分割,共60 Gy)使颅内病变部分缓解。然而,患者6个月后因颅内肿瘤进展死亡。
在成人眼内肿瘤的鉴别诊断中应考虑髓上皮瘤,尤其是在存在长期眼部症状的情况下。在某些病例中,这种疾病极具侵袭性。