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Case report
Positron emission tomography is moderately useful in the diagnosis of orbital metastasis

Celalettin Eroglu
,
Dilek Unal
,
Neslihan Kurtul
,
Ummuhan Abdulrezzak
,
M. Koray Gumu

Contemp Oncol (Pozn) 2014; 18
Data publikacji online: 2014/02/12
Plik artykułu:
- Positron emission.pdf  [0.09 MB]
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Introduction

Choroidal metastasis is the most common intraocular malignancy in adults [1–3]. It is seen in patients with advanced disease and is associated with poor prognosis [4]. In non-small cell lung cancer (NSCLC), choroidal metastasis is rare [5, 6]. Positron emission tomography (PET), which has been used in clinical practice in recent years, has proven useful in the diagnosis and following of many oncological diseases. In this case report, we aimed to emphasize the importance of PET for the diagnosis of choroidal metastasis, which is rarely seen in NSCLC.

Case report

A 37-year-old male patient presented with coughing. A chest X-ray revealed consolidation in the upper and middle zones of the left lung. Thorax computerized tomography (CT) scan showed bilateral multiple nodules, the largest of which were 24 mm and 16 mm in the upper lobe and the lower lobe of the left lung, respectively, as well as mediastinal lymph nodes, the largest of which was 19 mm, and pericardial fluid. The bronchoscopic biopsy pathology findings were compatible with squamous cell carcinoma. 18F-fluorodeoxyglucose (FDG)-PET-CT, which is used for the staging of primary malignant lesions, revealed primary malignant lesions located centrally in the left suprahilar, bilateral supraclavicular and mediastinal metastatic lymph nodes, which were prominent in the left lung, and multiple metastases in both surrenal glands and in the skeleton (intense FDG uptake, SUVmax values: 7–13). The patient, who was diagnosed with stage IV NSCLC, received 6 cycles of chemotherapy, including cisplatin and vinorelbine. The second PET-CT imaging revealed the regression of old lesions but with new metastatic lesions in the musculoskeletal system, intensive involvement in the orbital muscles of the right orbita, and increased FDG uptake (SUVmax: 3.6) in the posterior parts of the upper orbita (Fig. 1). Palliative radiotherapy was performed for metastatic bone lesions. The patient complained of blurred vision two weeks after the second PET-CT imaging (i.e. approximately 6 months after the diagnosis). Contrast-enhanced cranial CT was normal. Two amelanositic lesions in the upper temporal area in the right eye were detected during examination of the eyes. Therefore, fundus fluorescein angiography (Fig. 2) and optical coherence tomography imaging were performed, and these lesions were accepted as metastasis. These lesions were in favour of metastasis. Approximately two weeks after the start of blurred vision, an increase in mass size located centrally on the left suprahilar region with obstructive pneumopathy was established in a chest CT performed because of the shortness of breath. Palliative radiotherapy for lung mass and antibiotic treatment for obstructive pneumopathy were started. However, the patient died due to sepsis on the fourth day of thoracic radiotherapy.

Discussion

Positron emission tomography is a novel, useful imaging method that is increasingly being used for the diagnosis and staging of a series of tumours, detection of recurrence and assessment of therapeutic response. A combination of PET and CT improves the diagnostic capability of the method [7, 8].

Ocular tumours may be primary or metastatic. Ocular metastases occur frequently in the choroid. Choroidal metastasis may be single or multiple. Choroidal metastasis, which is seen rarely, is most commonly seen in breast and lung cancers. The incidence of ocular metastases of lung cancers has been reported to be 2–7% in the literature [9]. The diagnosis of ocular metastases is based on clinical findings supported by imaging techniques [9]. Ultrasonography reveals diffuse choroidal thickening with increased echogenicity and provides local extent of the tumour and may mimic amelanotic melanoma. However, it cannot certainly differentiate between the primary tumour and metastasis [10]. 18F-fluorodeoxyglucose PET/CT is a sensitive imaging modality to localize choroidal lesions. It provides the opportunity to detect small lesions or lesions in other organs not visible with other imaging modalities. In addition, it can help to differentiate metastatic from benign lesions and can detect metastatic lesions obscured by other processes or CT artefacts [11]. On the other hand, physiological FDG uptake in the ocular muscles is often seen, and, therefore, it may interfere with the detection of such small intraocular foci. In addition, it may not differentiate between choroidal melanoma and metastasis. However, in a known case of cancer with multi-organ involvement, such as in the present patient, the method virtually identifies intraocular metastasis.

Although the clinical findings refer to ocular metastasis, in this patient orbital metastasis was detected in the PET-CT evaluation performed to assess the response to the treatment of primary cancer before the appearance of its clinical findings.

Survival after the development of orbital metastasis is poor [9]. Consistent with this observation, this patient died within one month after the detection of orbital metastasis. Orbital metastasis should be kept in mind in the presence of increased FDG orbital uptake in PET-CT in patients with NSCLC, even in the absence of its clinical signs and symptoms.



Authors declare no conflict of interest.

References

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9. Asteriou C, Konstantinou D, Kleontas A, Paliouras D, Samanidis G, Papadopoulou F, Barbetakis N. Blurred vision due to choroidal metastasis as the first manifestation of lung cancer: a case report. World J Surg Oncol 2010; 8: 2.

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11. Donaldson MJ, Pulido JS, Mullan BP, Inwards DJ, Cantrill H, Johnson MR, Han MK. Combined positron emission tomography/computed tomography for evaluation of presumed choroidal metastases. Clin Experiment Ophthalmol 2006; 34: 846-51.



Address for correspondence



Dr. Dilek Unal

Erciyes Üniversitesi Tïp Fakültesi

M. Kemal Dedeman Onkoloji Hastanesi

38039, Kayseri, Türkiye

tel. 90-3522076666, fax 90-3524375807

e-mail: dilekunaldr@gmail.com



Submitted: 9.08.2012

Accepted: 7.11.2012
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