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although depending on the location and local destruction capacity&#44; it can cause compression or pathological fractures&#46; Generally&#44; it is a multiple lesion that preferentially affects the ribs&#44; clavicles&#44; mandible and pelvis<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a>&#59; orbital involvement is infrequent&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">We present the case of a 27-year-old woman with CKD secondary to nephronoptisis that underwent 2 renal transplants&#44; the first one anticipated at 7 years of age and the second at 9 years&#44; with loss of both due to chronic graft nephropathy&#46; She finally started hemodialysis at 23 years of age&#46; After 4 years on hemodialysis and with a history of more than 5 months of evolution&#44; the patient showed severe secondary HP with a maximum PTHi of 4876<span class="elsevierStyleHsp" style=""></span>pg&#47;ml&#44; hypercalcemia and normo- and hyperphosphatemia that is not controlled despite treatment with cinacalcet&#44; vitamin D analogs and phosphate binders&#46; 99mTc-sestamibi scan shows pathological uptake of the radiotracer in all parathyroid glands demonstrating a polyglandular hyperplasia&#46; In addition&#44; physical examination is remarkable for the progressive and pronounced appearance of an exophthalmos with caudal displacement of the left orbit and a decrease in vision&#46; Reconstructive orthopedic CT &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41; and MRI describe several cystic-looking bone radiolucent lesions of 3 left periorbital brown tumors located respectively in the orbit ceiling with extension to the ipsilateral frontal sinus&#44; In the left upper jaw and in the ascending branch of the left mandible with secondary arterial occlusion&#46; With these findings&#44; a total parathyroidectomy was performed with suprasternal autotransplantation to control 2nd HPTH and to achieve the reduction of tumors&#46; After the intervention&#44; PTHi levels fall rapidly with development of a hungry bone syndrome that requires high doses of calcium&#44; vitamin D and hemodialysis with calcium of 1&#46;75<span class="elsevierStyleHsp" style=""></span>&#956;mol&#47;l&#44; which ensures the success of the intervention&#46; Two months later&#44; the analytical improvement is not accompanied by reduction of clinical symptoms&#59; exophthalmos and compressive optic neuropathy continues&#46; The CT scan shows an increase in size of the orbital ceiling lesion requiring excision&#46; Microscopic examination revealed brown bone tumor&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">At present&#44; only 19 cases have been described with periorbital involvement&#46; In most cases&#44; tumor excision is performed&#44; although other different locations are described in which with the total parathyroidectomy has been followed by remission of the bone lesion&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">3&#8211;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Our case was resolved with parathyroidectomy and tumor excision &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The prevalence of brown tumor in patients with 2ndHPTH is 1&#46;5&#8211;13&#37; in CKD&#44;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">1</span></a> being more frequent in young women&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">6</span></a> However&#44; a cautious differential diagnosis should be made and rule out bone tumor implants&#46; Nowadays&#44; the measurement of and the effective treatment of 2ndHPTH&#44; the appearance of new cases is decreasing&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">7</span></a></p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span>"
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Letter to the Editor
Exophthalmos and hyperparathyroidism
Exoftalmos e hiperparatiroidismo
María Teresa Mora Moraa,
Corresponding author
maytemorabis@hotmail.com

Corresponding author.
, Jesús Pedro Marín Álvarezb
a Sección de Nefrología, Complejo Hospitalario Universitario de Huelva, Huelva, Spain
b Sección de Nefrología, Hospital San Pedro de Alcántara, Cáceres, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">The brown tumor&#44; also known as osteoclastoma&#44; is a local and benign lesion of the bone&#46; It appears as a consequence of an increase in osteoclastic activity and fibroblastic proliferation in the context of severe primary or secondary hyperparathyroidism &#40;2ndHPTH&#41;&#44; the latter occurring in chronic kidney disease &#40;CKD&#41; due to decreased vitamin activity D at the renal level&#44; with decreased phosphorus excretion and a tendency to hypocalcemia&#44; which stimulates the growth of parathyroid glands&#46; By microscopy the brown tumor is characterized by an increase in osteoclast activity&#44; expansion of bone resorption and formation of new bone tissue&#59; there are irregularities in the of the trabecular tissue thickness and peritrabecular fibrosis&#46; The presence of multinucleated giant cells and interstitial hemorrhage with hemosiderin deposits gives it the characteristic brown appearance&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">1&#44;2</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">Complete regression or disappearance of the brown tumor usually occurs after parathyroidectomy&#44; although depending on the location and local destruction capacity&#44; it can cause compression or pathological fractures&#46; Generally&#44; it is a multiple lesion that preferentially affects the ribs&#44; clavicles&#44; mandible and pelvis<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a>&#59; orbital involvement is infrequent&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">We present the case of a 27-year-old woman with CKD secondary to nephronoptisis that underwent 2 renal transplants&#44; the first one anticipated at 7 years of age and the second at 9 years&#44; with loss of both due to chronic graft nephropathy&#46; She finally started hemodialysis at 23 years of age&#46; After 4 years on hemodialysis and with a history of more than 5 months of evolution&#44; the patient showed severe secondary HP with a maximum PTHi of 4876<span class="elsevierStyleHsp" style=""></span>pg&#47;ml&#44; hypercalcemia and normo- and hyperphosphatemia that is not controlled despite treatment with cinacalcet&#44; vitamin D analogs and phosphate binders&#46; 99mTc-sestamibi scan shows pathological uptake of the radiotracer in all parathyroid glands demonstrating a polyglandular hyperplasia&#46; In addition&#44; physical examination is remarkable for the progressive and pronounced appearance of an exophthalmos with caudal displacement of the left orbit and a decrease in vision&#46; Reconstructive orthopedic CT &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41; and MRI describe several cystic-looking bone radiolucent lesions of 3 left periorbital brown tumors located respectively in the orbit ceiling with extension to the ipsilateral frontal sinus&#44; In the left upper jaw and in the ascending branch of the left mandible with secondary arterial occlusion&#46; With these findings&#44; a total parathyroidectomy was performed with suprasternal autotransplantation to control 2nd HPTH and to achieve the reduction of tumors&#46; After the intervention&#44; PTHi levels fall rapidly with development of a hungry bone syndrome that requires high doses of calcium&#44; vitamin D and hemodialysis with calcium of 1&#46;75<span class="elsevierStyleHsp" style=""></span>&#956;mol&#47;l&#44; which ensures the success of the intervention&#46; Two months later&#44; the analytical improvement is not accompanied by reduction of clinical symptoms&#59; exophthalmos and compressive optic neuropathy continues&#46; The CT scan shows an increase in size of the orbital ceiling lesion requiring excision&#46; Microscopic examination revealed brown bone tumor&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">At present&#44; only 19 cases have been described with periorbital involvement&#46; In most cases&#44; tumor excision is performed&#44; although other different locations are described in which with the total parathyroidectomy has been followed by remission of the bone lesion&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">3&#8211;5</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Our case was resolved with parathyroidectomy and tumor excision &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The prevalence of brown tumor in patients with 2ndHPTH is 1&#46;5&#8211;13&#37; in CKD&#44;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">1</span></a> being more frequent in young women&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">6</span></a> However&#44; a cautious differential diagnosis should be made and rule out bone tumor implants&#46; Nowadays&#44; the measurement of and the effective treatment of 2ndHPTH&#44; the appearance of new cases is decreasing&#46;<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">7</span></a></p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Mora Mora MT&#44; Mar&#237;n &#193;lvarez JP&#46; Exoftalmos e hiperparatiroidismo&#46; Nefrolog&#237;a&#46; 2017&#59;37&#58;441&#8211;443&#46;</p>"
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Idiomas
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