- Case report
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A case with transient refractive change after removal of pituitary tumor
BMC Ophthalmologyvolume 13, Article number: 65 (2013)
Refractive change can be caused by systemic illnesses such as Lupus erythematosus, thyroid deficiency, and diabetes mellitus. However, refractive change after pituitary tumor removal has so far not been reported.
A 62-year-old woman presented with blurred near vision 10 days after trans-sphenoidal surgery (TSS) for a pituitary tumor. Around the same time, she experienced intercurrent hyponatremia. The corrected visual acuity of both eyes was 20/20, the spherical equivalent of the right eye was −2.125 diopters, and of the left eye was −2.0 diopters before TSS. However, 11 days after TSS, the spherical equivalent of the right eye changed to −0.75 diopters, and that of left eye changed to −1.125 diopters without hyperglycemia. There were no changes in the corrected visual acuity during the follow-up.
We demonstrated a case with transient refractive change after TSS. The following mechanism is proposed: Hyponatremia induced by the pituitary tumor removal causes an osmotic change in the aqueous humor with lens swelling. This case report is a reminder to both ophthalmologists and neurosurgeons that ophthalmological factors such as lens thickness and axial length should be taken into account when conducting preoperative examinations especially for patients undergoing TSS.
Refractive change of the eye is affected by a combination of axial length, corneal power anterior chamber depth and lens power. In general, refraction changes with age. In a recent report about lens power and refractive error, the axial length and the lens power was found to influence the refractive error mostly in adults aged over 50 [1, 2].
Refractive change is often described in systemic illness such as Lupus erythematosus , thyroid deficiency , pregnancy, orbital tumor , and diabetes mellitus (DM). Refractive change has been recognized in DM since the 19th century and was well-described throughout the 20th century [6–10].
The pathologic occurrence of refractive change falls under two patterns: one is lens thickness changing due to an abnormal metabolic process, and the second is a change of eye ball shape caused by an increase of orbital contents. Lupus erythematosus and DM cause abnormal water metabolism and influx of aqueous humor from the anterior chamber into the lens, culminating in an increased lens thickness [3, 6–10]. Thyroid deficiencies and orbital tumors increase orbital contents due to inflammation or a tumor, compressing the eye ball. As a result, the eye ball shape is altered, which in turn produces refractive change [4, 5].
To date, refractive change in hyponatremia after trans-sphenoidal surgery (TSS) has never been reported. In this case, we report the refractive change following TSS, and discuss the causal correlation between refractive change and hyponatremia.
A 62-year-old woman complaining of dizziness was admitted to our college hospital. The patient had a past medical history of thyroid dysfunction. She was neurologically intact, and had no abnormalities in her blood tests. Magnetic resonance imaging (MRI) showed an extended intrasellar tumor, which measured 25-mm in its greatest diameter and did not attach to the optic chiasm. The lesion infiltrated the right cavernous sinus, and extended to the pharynx (Figure 1a). Initially, the tumor was considered to be a nonfunctional pituitary adenoma.
The patient consented to TSS, and TSS was performed without incident (Figure 1b). Seven days after TSS, the patient presented with associated hyponatremia (Figure 2). Approximately, 10 days after TSS, the patient complained of blurred near vision.
In the ophthalmological examination before TSS, her vision was almost completely intact without visual field loss. The corrected visual acuity of both eyes was 20/20, the spherical equivalent of the right eye was −2.125 diopters, and that of the left eye was −2.0 diopters before TSS. However, 11 days after TSS, the spherical equivalent of the right eye had changed to −0.75 diopters, and that of the left eye had changed to −1.125 diopters. Figure 2 shows the time course of serum electrolyte and glucose levels, corneal radius, spherical equivalent, axial length, anterior chamber depth, and lens thickness of both eyes. Axial length, anterior chamber depth and lens thickness were calculated by A-mode ultrasonography. Lens power was calculated with Bennett’s formula  at the onset of blurred vision (11 days after surgery) and follow up (264 days), but could not be calculated before onset (i.e. before surgery and upto 10 days after) because we did not calculate axial length, anterior chamber depth and lens thickness over this time frame. There were no changes in axial length during follow up; however, both spherical equivalent and lens thickness were decreased, while in contrast the anterior chamber depth was increased. In addition, the size of both the decrease in lens thickness and the increase in anterior chamber depth was the same. The lens power (right eye: 17.52 diopters, left eye: 18.30 diopters) at onset increased to 20.27 diopters (right eye) and 20.11 diopters (left eye) at follow up (Table 1). Although her hyponatremia rapidly improved over a period of one week, the refractive change persisted for 6 weeks (43 days) after TSS and 4 weeks after onset. During her 7 months of follow-up, the level of serum glucose was not changed from a normal and the patient had no apparent recurrence. And also, the corrected visual acuity was not changed during the follow-up.
Many ophthalmological reports have documented transient refractive change in systemic illness. However, this report is the first to present the hyperopia after TSS with hyponatremia. In DM, the main mechanism underlying refractive change has been implicated in which decreasing osmotic pressure of the aqueous humor causes consequent hydration of the lens [6–10]. In our patient, the average spherical equivalent of both eyes in the first visit was −2.06 diopters, at the time of initial complaint of blurred near vision was −0.95 diopters, and at approximately 6 months after onset had returned to the initial level. During the same time period, the average lens thickness of both eyes upon onset was 4.1 mm, and decreased to 3.9 mm 6 months after onset, implying that the lens was swelling and reverted to the initial thickness by 6 months. The patient exhibited no change in axial length throughout the studied time course. The most important fact in this case was that hyperopia and hyponatremia occurred simultaneously after TSS.
We found increased lens thickness and hyperopic shift after the hyponatremia in the present study. There are some concerns about the relationship between the refractive change and the related factors. Generally, increased lens thickness alone should result in a myopic shift.
Firstly, we need to consider the ciliary processes and the position of the lens. The anterior shift of the lens-iris diaphragm was able to cause myopia . The posterior pole of the lens calculated as anterior chamber depth + lens thickness did not change during the study period (Table 1). The increase in lens thickness caused by hyponatremia matches the decrease in anterior chamber depth. If the lens swelling in its position is sustained by the zonule and the ciliary processes, the amount of a backward movement of the posterior pole could be at least equal to half the increase in lens thickness. With increasing age, the posterior pole recedes a little and the anterior chamber decreases by a similar amount leaving the lens in its usual position . However, the present case showed that the posterior pole of the lens did not recede, suggesting that the refractive change was not due to changes in lens position.
Next, we consider both the corneal power and lens power during follow up. The corneal power was not changed. In contrast, the lens power at onset was less than during follow up according to Bennett’s formula (Table 1), suggesting that the lens has lost the power with swelling.
Preoperative ophthalmologic examination before TSS is common. Routine examinations measure visual acuity, visual fields, and ocular pressure. However, we rarely get the opportunity to evaluate lens thickness and axial length. In this case, the hyperopic shift was caused by an increase in the lens thickness. Factors such as lens thickness and axial length should be taken into account when conducing preoperative ophthalmologic examinations especially for patients undergoing TSS.
Written informed consent was obtained from the patient for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
HI conceived of the study and drafted the manuscript. JA critically revised the manuscript. KU performed the neurosurgery, collected the data, and helped to draft the manuscript. NI, TI, and CVB participated in the design of the study and helped to draft the manuscript. OM was involved in drafting the manuscript and participated in its design and coordination, and has given final approval of the version to be published. All authors read and approved the final manuscript.
Magnetic resonance imaging.
Iribarren R, Morgan IG, Nangia V, Jonas JB: Crystalline lens power and refractive error. Invest Ophthalmol Vis Sci. 2012, 53 (2): 543-550. 10.1167/iovs.11-8523.
Hashemi H, Iribarren R, Morgan IG, Khabazkhoob M, Mohammad K, Fotouhi A: Increased hyperopia with ageing based on cycloplegic refractions in adults: the Tehran Eye Study. Br J Ophthalmol. 2010, 94 (1): 20-23. 10.1136/bjo.2009.160465.
Shu U, Takeuchi F, Tanimoto K, Moroi Y, Uchida K, Ito K: Transient myopia with severe chemosis associated with exacerbation of disease activity in systemic lupus erythematosus. J Rheumatol. 1992, 19 (2): 297-301.
Chandrasekaran S, Petsoglou C, Billson FA, Selva D, Ghabrial R: Refractive change in thyroid eye disease (a neglected clinical sign). Br J Obstet Gynaecol. 2006, 90 (3): 307-309.
Friberg TR, Grove AS: Choroidal folds and refractive errors associated with orbital tumors. An analysis. Arch Ophthalmol. 1983, 101 (4): 598-603. 10.1001/archopht.1983.01040010598014.
Wiemer NG, Eekhoff EM, Simsek S, Heine RJ, Ringens PJ, Polak BC, Dubbelman M: Refractive properties of the healthy human eye during acute hyperglycemia. Graefes Arch Clin Exp Ophthalmol. 2008, 246 (7): 993-998. 10.1007/s00417-008-0810-y.
Wiemer NG, Dubbelman M, Kostense PJ, Ringens PJ, Polak BC: The influence of diabetes mellitus type 1 and 2 on the thickness, shape, and equivalent refractive index of the human crystalline lens. Ophthalmology. 2008, 115 (10): 1679-1686. 10.1016/j.ophtha.2008.03.019.
Okamoto F, Sone H, Nonoyama T, Hommura S: Refractive changes in diabetic patients during intensive glycaemic control. Br J Ophthalmol. 2000, 84 (10): 1097-1102. 10.1136/bjo.84.10.1097.
Saito Y, Ohmi G, Kinoshita S, Nakamura Y, Ogawa K, Harino S, Okada M: Transient hyperopia with lens swelling at initial therapy in diabetes. Br J Ophthalmol. 1993, 77 (3): 145-148. 10.1136/bjo.77.3.145.
Eva PR, Pascoe PT, Vaughan DG: Refractive change in hyperglycaemia: hyperopia, not myopia. Br J Ophthalmol. 1982, 66 (8): 500-505. 10.1136/bjo.66.8.500.
Bennett AG: A method of determining the equivalent powers of the eye and its crystalline lens without resort to phakometry. Ophthalmic Physiol Opt. 1988, 8 (1): 53-59.
Ikeda N, Ikeda T, Nagata M, Mimura O: Pathogenesis of transient high myopia after blunt eye trauma. Ophthalmology. 2002, 109 (3): 501-507. 10.1016/S0161-6420(01)00995-2.
Dubbelman M, van der Heijde GL, Weeber HA: The thickness of the aging human lens obtained from corrected Scheimpflug images. Optom Vis Sci. 2001, 78 (6): 411-416. 10.1097/00006324-200106000-00013.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2415/13/65/prepub
None of the authors have received funding for this study. We thank Dr. David Eve (University of South Florida) for his English editing of the manuscript.
The authors declare that we have no competing interests.