Bone Dysmorphia-Induced Blindness Following a Secondary Hyperparathyroidism: A Case Report

Introduction: Conjunctival-corneal or choroidal calcifications are frequent in SHPT, blindness is however exceptional. We report a case of blindness secondary to compressive ischemic optic neuropathy. Case Report: Mr. B.E.K., 49 years old, has a chronic renal failure secondary to unlabeled glo-merular nephropathy for 17 years. He has been on chronic hemodialysis for 12 years and has had SHPT for nine years. He secondarily developed disabl-ing segmental osteoarticular deformities associated with kyphoscoliosis, “drumstick” fingers and facial dysmorphism. Five months before admission he developed eye pain and reduced visual acuity progressing within one month to blindness. Biology noted: serum creatinine at 726 umol/l (60 - 120 umol/L), azotemia at 14.3 mmol/l (2.5 - 7.5 mmol/L), serum calcium at 2.25 (2.25 - 2.55 mmol/L), phosphatemia at 1.13 (0.8 tion of SHPT, in order to avoid its major complications, such as blindness, especially since current preventive and curative measures have proven their effectiveness.


Introduction
Secondary hyperparathyroidism (SHPT) is a common complication of chronic kidney disease, usually caused by abnormal phosphocalcic metabolism. Prolonged dialysis causes the development of CKD-mineral and bone disorder (CKD-MBD) [1] [2] [3] responsible for musculoskeletal lesions of various locations, especially brown tumors (1.5% to 1.7%). The localization of these lesions at the orbital level, with blindness as a complication, is exceptional [4] [5] [6]. We report a case of blindness after ischemic optic neuropathy by orbital compression.

Case Report
We report a case of a 49-year-old patient with a history of chronic renal failure (CRF) for 17 years secondary to unlabeled nephropathy, on hemodialysis for 12 years.
He has no history of diabetes or old high blood pressure. He was operated on for appendicitis when he was 20 years old. He has regular dialysis, 3 sessions per week and for a duration of four hours each on a left humeral arteriovenous fistula. The calcium in the dialysate is 1.75 mmol/l. The phosphocalcic balance at the initiation of dialysis notes a parathyroid hormone (PTH) level of 137 pg/ml (normal value: 10 -60 pg/ml), serum calcium: 1.73 mmol/l, phosphoremia of 2.28 mmol/the. The concentration of 25-OH-vitamin D is 16 ng/ml (normal value: 20 -50 ng/ml). Clinically, the arterial pressure is balanced under antihypertensive treatment, the average interdialytic weight gain is 1.5 Kg with a dry weight of 60 Kg. The mean dialysis dose (Kt/v) is greater than or equal to 1.2.
Eight years after dialysis, segmental and axial osteoarticular deformities and pathological fractures of the limbs gradually occur. Biology shows an increased PTH level up to 1341 ng/ml, calcium level at 2.18 mmol/l, phosphoremia at 1.91 mmol/l, 25-OH vitamin D of 32 ng/ml. Standard radiographs show diffuse bone demineralization. Non-compliance with its treatment with calcium carbonate and alphacalcidiol was observed. Calcimimetics were not available. The rate of biological monitoring was irregular.
Five months prior to admission, he presented with eye pain with reduced visual acuity, which was symmetrical and gradually worsening; having progressed to blindness after one month. Clinical examination on admission revealed dis-Open Journal of Nephrology abling axial and segmental osteoarticular deformities with kyphoscoliosis, "drumstick" fingers and facial dysmorphism; bilateral blindness with optic atrophy in the fundus; there were no other signs of neurological focus or cardiorespiratory disorders. A picture of optic neuropathy associated with a generalized dysmorphic syndrome on SHPT was captured.
In addition, a cranioencephalic and orbital MRI made it possible to highlight diffuse brown tumors of the cranial vault with a thickening of the skull bases and a pre-chiasmatic optic atrophy ( Figure 2).
Retinal angiography revealed lesions suggestive of compressive ischemic optic neuropathy (Figure 3). From those findings we retained the diagnosis of blindness due to ischemic optic neuropathy, secondary to CKD-MBD, compressive of the optic channels.
Our patient presented with a complicated CKD from SHPT by CKD-MBD. He presents with osteoarticular deformities, pathological fractures and facial dysmorphism. These manifestations have been reported by other authors and are thought to be due to CKD-MBD [1] [3] [8] [9] [10]. Other manifestations have also been reported, such as bone and joint pain, pruritus [1] [3].
Our patient also presents bilateral blindness, which represents the peculiarity of our observation. Indeed: Orbito-ocular involvement is a rare complication of Blindness due to ischemic neuropathy secondary to orbital compression, such as apical stenosis, is exceptional [5] [6], CKD-MBD responsible for thickening and brown tumors of the base of the skull (1% -2%) are the most frequent causes. Lesions secondary to brown orbital tumors are much rarer (1.5% to 13% CKD) and essentially ethmoidal [2] [5] [6]. Brown tumors are purely lytic lesions with poor bone formation [6]. They variably associate bone resorption and osteosclerosis, and can reach a sufficient volume and blow the cortex [2].
In our patient, the compression that caused the blindness was secondary to a reduction in the size of the optic channels by thickening of the skull base. The elevated levels of ALP and PTH, as well as the normal calcium and phosphatemia, found in our case, have been reported by other studies [1] [8]. Indeed, hypercalcemia is intermittent, hypercalcemia and hyperphosphatemia can also be observed. However, the level of PTH did not show a correlation with clinical severity and imaging [4].

Conclusion
Such advanced forms of secondary hyperparathyroidism are increasingly rare. This observation underlines the importance of early detection of SHPT, in order to avoid its major complications, such as blindness, especially since current preventive and curative measures have proven their effectiveness.

Conflicts of Interest
The authors declare no conflicts of interest regarding the publication of this paper.