Nasopharyngeal carcinoma (NPC) in the ophthalmic practice: A serious neoplasm presenting initially to ophthalmologists

被引:3
作者
Alrashed, Saleh H. [1 ]
Alkatan, Hind M. [1 ,2 ,3 ]
Alarfaj, Motazz [4 ,7 ]
Alnahdi, Muhannad A. [5 ]
Almeshari, Nawaf Z. [6 ]
Almutairi, Faris J. [6 ]
Maktabi, Azza M. Y. [5 ]
机构
[1] King Saud Univ, Coll Med, Dept Ophthalmol, Riyadh, Saudi Arabia
[2] King Saud Univ, Coll Med, Dept Pathol & Lab Med, Riyadh, Saudi Arabia
[3] King Saud Univ, Dept Ophthalmol, King Saud Univ Med City, Riyadh, Saudi Arabia
[4] King Khalid Eye Specialist Hosp, Dept Pathol & Lab Med, Riyadh, Saudi Arabia
[5] King Saud Bin Abdulaziz Univ Hlth Sci, Coll Med, Riyadh, Saudi Arabia
[6] King Saud Univ, Coll Med, Riyadh, Saudi Arabia
[7] Imam Abdulrahman Bin Faisal Univ, Coll Med, Dept Ophthalmol, Dammam, Saudi Arabia
关键词
Cranial nerve palsy; diplopia; nasopharyngeal carcinoma; orbital invasion;
D O I
10.4103/1319-4534.343369
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PURPOSE: Nasopharyngeal carcinoma (NPC) is an aggressive malignant tumor that arises from the nasopharyngeal epithelial lining. Most patients with NPC present with a neck mass or cranial nerve palsy. It is infrequent for patients with NPC to present to an ophthalmologist initially with ophthalmic complaints and absence of prior diagnosis of NPC. We are reporting a series of six NPC cases that presented solely with ophthalmic complaints, to attract the attention of ophthalmologist to such a serious neoplasm. METHODS: A retrospective observational study of all consecutive patients diagnosed with NPC based on their initial ophthalmic presentation with no prior diagnosis of this neoplasm. Patients presented for the first time to two tertiary eye hospitals. Data were collected by the chart review for demographics, clinical presentation, radiological imaging, treatment regimen, and follow-up. Histopathological review of their tissue specimens was conducted by two pathologists. RESULTS: We had six patients who presented for the first time to our ophthalmic service complaining mostly of limitation of extraocular muscle motility with or without diplopia (4/6), orbital or facial pain (2/6), and disturbance in vision (2/6). The age ranged from 35 to 92 years with a mean of 58 years. A male predominance was observed with male-to-female ratio of 5:1. The cases are described along with their imaging and histopathological findings. Relevant literature review was also presented. Most of our patients (5/6) received combination of radiotherapy and chemotherapy. One patient refused treatment and 2 eventually passed away after 7 months. CONCLUSION: Ophthalmologists may play a major role in diagnosing such patients accurately and referring them for early management and better prognosis.
引用
收藏
页码:225 / 229
页数:5
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