Abstract
Bilateral macular hole is a rare secondary effect of tamoxifen, a condition which is probably underdiagnosed. We describe the case of a 63-year-old woman who had received low-dose treatment with tamoxifen for 10 years. She presented with a best-corrected visual acuity of 20/40 in both eyes and bilateral macular hole with posterior hyaloid attachment. No reflective deposits were observed. A 23-gauge pars plana vitrectomy with internal limiting membrane peeling and gas tamponade was performed in the right eye with no anatomical or functional improvement. The most accepted mechanism of macular hole related to tamoxifen is Müller cell toxicity with retinal tissue loss. Therefore, it seems that the standard procedure used in idiopathic macular hole is not the optimal choice, due to a different pathogenic mechanism.
Introduction
Tamoxifen is a non-steroidal selective estrogen receptor modulator used as adjuvant endocrine therapy in estrogen receptor-positive breast cancer. This drug can induce some ocular complications such as crystalline maculopathy, macular edema, retinal vein occlusions, bilateral optic neuritis, and corneal opacities [1]. Recently, some studies have demonstrated that low-dose treatment can be extended up to 10 years, as tamoxifen can reduce relapse of cancer in patients at high risk of recurrence [2]. A relationship between the development of macular hole (MH) and low-dose tamoxifen (usually considered a cumulative dose <100 g) has been recently described [3-8], but the management remains controversial.
Case Report
A 63-year-old woman with a history of breast cancer presented with mild, progressive, bilateral visual loss for years with no prior ocular history. The patient had received 20 mg of tamoxifen daily for approximately 10 years (cumulative dose around 73 g). She began with this adjuvant therapy following a mastectomy, which had been done rapidly after diagnosis at age 41. Therefore, she had not received tamoxifen for 12 years at presentation. Her best corrected visual acuity was 20/40 in both eyes (BE). Slit lamp examination of the anterior segment was unremarkable. Dilated fundus examination showed an irregular foveal light reflex with pseudohole appearance and no evidence of reflective deposits in the inner layers, which excluded crystalline maculopathy (Fig. 1a, b). Spectral-domain optical coherence tomography (SD-OCT) showed a bilateral MH with a thin overlying roof of inner retinal remnant. Some small cystic spaces on the edges of the hole and attachment of the posterior hyaloid (PH) were also observed with no evidence of thickening or macular edema (Fig. 1c, d). Fluorescein angiography (FA) showed a progressive and diffuse hyperfluorescence in the fovea of BE with no late phase leakage (Fig. 2). FA allows to differentiate retinal changes related to tamoxifen retinopathy, which may be similar on SD-OCT to the ones found in macular telangiectasia type 2 (MacTel2) [9]. Nevertheless, a late leakage of telangiectatic macular capillaries is observed in FA of eyes with MacTel2 [10]. Thus, the diagnosis of bilateral MH related to tamoxifen toxicity was made.
A 23-gauge pars plana vitrectomy (PPV) with internal limiting membrane (ILM) peeling and sulfur hexafluoride (SF6) 24% gas tamponade was performed in the right eye (RE). The patient rested in prone position for 6 days. The MH remained opened with elevated edges after surgery (Fig. 3). A second 23-gauge PPV was proposed, but the patient rejected it. The patient has been followed for 4 years with no changes in visual acuity (best corrected visual acuity of 20/40 in BE) or SD-OCT images.
Discussion
The incidence of MH due to tamoxifen toxicity is expected to increase as the tendency is to extend low-dosage tamoxifen treatment. Furthermore, the increasing use of SD-OCT will probably raise the number of cases.Surgical outcome of secondary MH related to tamoxifen toxicity remains unclear. It is worth noticing that in our case BE showed still attached PH, which suggests a different pathomechanism from idiopathic MH, where anteroposterior and tangential traction forces after posterior vitreous detachment are thought to be the main cause of this condition. Therefore, it seems that in this type of secondary MH the standard procedure used in idiopathic MH (i.e., PPV with ILM peeling and gas tamponade) would not be effective, as it seems more related to degenerative mechanisms that lead to tissue loss in the retina. The most accepted mechanism of MH related to tamoxifen is that toxic damage culminates in axonal degeneration leading to Müller cell impairment. It may cause intraretinal foveolar cysts, which in turn would predispose MH formation [11].
Due to the increasing use of SD-OCT and the new trend to extent low-dosage treatment, foveolar cavitations with outer retinal defect and MH related to tamoxifen have been described [4, 5, 7, 8]. In 2005, Gualino et al. [3] first described this complication, and additionally in the same year, Cronin et al. [6] reported a retrospective analysis of 300 consecutive cases of MH and concluded that there was a statistically increased incidence of MH in women treated with tamoxifen.
Concerning the crystalline deposits status in low-dose tamoxifen toxicity, crystalline retinopathy has classically been thought to be the hallmark of tamoxifen toxicity. This association was based on patients treated with high-dose tamoxifen [12]. Superficial crystals have also been observed in patients with early cavitary spaces. Furthermore, more advanced cavitations without visible crystals have been demonstrated in patients who received low-dose tamoxifen [5, 7]. Thus, crystalline maculopathy could represent an earlier finding in tamoxifen toxicity with initial Müller cell damage, while foveal cavitations could correspond to a later stage of atrophy where the crystals have degenerated. Doshi et al. [7] also suggested this possibility after reporting the case of a woman who had received a cumulative dose of tamoxifen of 18.25 mg with evidence of ILM draping with prominent crystals and a small cavitary space in the central fovea on the RE. On the contrary, the left eye of the same patient did not show any visible crystals, although a nearly full thickness cavitation was demonstrated [7]. Therefore, the absence of crystals in the posterior pole might be a common manifestation of late stages of low-dose tamoxifen maculopathy, although more longitudinal follow-up studies are needed to confirm this hypothesis.
Regarding the treatment, Chung et al. [5] reported MH closure and visual improvement in two patients with MH related to systemic antiestrogen agents through surgery with solely 23-gauge PPV and ILM peeling, although crystalline deposits were not found and there was no description about PH membrane status. Even though, Bernstein and DellaCroce [13] also presented the case of a woman who had received tamoxifen with bilateral MH coexisting with crystalline maculopathy who had a previous failed surgery on her RE elsewhere, which was not detailed. A new surgery on her RE with perfluoropropane (C3F8) tamponade successfully closed the MH. Nevertheless, the same surgery was performed on her left eye with no improvement and persistent MH on following examinations [13].
Conclusion
We suggest that observation of MH related to low-dose tamoxifen is a feasible option at this time due to poor functional results after vitrectomy and ILM peeling found in our case and the previous case described by Bernstein and DellaCroce [13]. Nevertheless, more studies are needed in order to understand the evolution of tamoxifen associated with MH, possible precursor lesions, and their optimal management.
Patients with reduced visual acuities may not be aware of their visual deficits initially, as in our case. Macular cavitations and holes due to tamoxifen may occur in the absence of subjective visual complaints. Hence, we strongly recommend – whenever possible – a complete ophthalmologic exam including SD-OCT in those patients under treatment with tamoxifen, regardless of subjective absence of visual impairment.
Finally, if any macular cavitations are observed, a FA should be performed in order to exclude MacTel2. Thus, if any sign of retinal toxicity is detected promptly in those patients under treatment with tamoxifen, progressive visual acuity deterioration could be avoided by considering tamoxifen discontinuation in agreement with the oncologist after considering the risk-benefit profile in each individualized case.
Statement of Ethics
Verbal and written informed consent was obtained from the patient for publication of this case report and all accompanying images.
Conflict of Interest Statement
The authors have no conflict of interest to declare.
Funding Sources
Not applicable.
Author Contributions
All authors collected and interpreted the patient’s clinical findings. N.T.B. and J.I.V.S. contributed to the writing and editing of the manuscript. N.T.B. reviewed the literature. All authors read and approved the final version of the manuscript.