Shikishima Keigo, Miyake Akira, Ikemoto Isao, Kawakami Makio
Department of Ophthalmology, Jikei University School of Medicine, Tokyo, Japan.
Department of Urology, Jikei University School of Medicine, Tokyo, Japan.
Jpn J Ophthalmol. 2006 Sep-Oct;50(5):469-473. doi: 10.1007/s10384-006-0342-0.
To demonstrate the pathological features of the extremely rare metastatic transitional cell carcinoma (TCC) from the bladder to the orbit, and to review the literature on metastatic TCC to the orbit.
A 74-year-old man experienced 2 weeks of red eye, proptosis, diplopia, pain, and visual loss in the right eye. Three years previous to the current presentation, the patient had undergone a transurethral resection for superficial and moderately differentiated TCC of the bladder. A transseptal anterior orbitotomy was performed.
Histopathological examination of the orbital lesion revealed nests of carcinomatous cells. Atypical pleomorphic cells with vacuolated cytoplasm were evident. The cellular morphology of the orbital lesion was identical to that of the primary TCC. There have been 12 previously reported cases of metastases to the orbit from TCC of the bladder, with the time from onset of primary TCC to observation of ocular symptoms ranging from 3 weeks to 11 years. Mean survival after orbital metastasis developed from TCC was 3.0 months.
This study presents a detailed description of the pathological features of metastatic TCC in the orbit. In cases of orbital metastasis from TCC, patient prognosis is very poor.
展示极为罕见的膀胱移行细胞癌(TCC)转移至眼眶的病理特征,并回顾有关眼眶转移性TCC的文献。
一名74岁男性出现右眼眼红、眼球突出、复视、疼痛及视力丧失2周。本次就诊前3年,该患者曾因膀胱浅表及中度分化TCC接受经尿道切除术。实施了经鼻中隔前路眼眶切开术。
眼眶病变的组织病理学检查显示癌细胞巢。可见具有空泡状细胞质的非典型多形性细胞。眼眶病变的细胞形态与原发性TCC相同。此前已有12例膀胱TCC转移至眼眶的报道,从原发性TCC发病至出现眼部症状的时间为3周至11年。TCC发生眼眶转移后的平均生存期为3.0个月。
本研究详细描述了眼眶转移性TCC的病理特征。在TCC发生眼眶转移的病例中,患者预后很差。