Regression of orbital brown tumor after surgical removal of parathyroid adenoma

Brown tumors are rare skeletal manifestations that occur in less than 2% of primary hyperparathyroidism (PHPT) cases. Even rarer is the occurrence of brown tumor of the orbit, and few cases have been reported around the world. The rare instance of this benign tumor has prompted us to report the case...

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Main Authors: Felipe Martins de Oliveira, Tiago Eidy Makimoto, Nilza Maria Scalissi, Marília Martins Silveira Marone, Sergio Setsuo Maeda
Format: Article
Language:English
Published: Brazilian Society of Endocrinology and Metabolism 2015-08-01
Series:Archives of Endocrinology and Metabolism
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972015000500455&lng=en&tlng=en
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spelling doaj-e089eb5fc0a54b5eb60c0cb779d1f6ee2020-11-24T20:42:10ZengBrazilian Society of Endocrinology and MetabolismArchives of Endocrinology and Metabolism2359-42922015-08-0159545545910.1590/2359-3997000000088S2359-39972015000500455Regression of orbital brown tumor after surgical removal of parathyroid adenomaFelipe Martins de OliveiraTiago Eidy MakimotoNilza Maria ScalissiMarília Martins Silveira MaroneSergio Setsuo MaedaBrown tumors are rare skeletal manifestations that occur in less than 2% of primary hyperparathyroidism (PHPT) cases. Even rarer is the occurrence of brown tumor of the orbit, and few cases have been reported around the world. The rare instance of this benign tumor has prompted us to report the case and treatment of an orbital brown tumor in a patient with PHPT caused by parathyroid adenoma. We present the case of a patient undergoing follow-up at a referral center. The 60-year-old female patient, presented herself with progressive swelling in the nasal region, epistaxis and proptosis, she had noticed seven months prior to our examination. Multiple imaging and laboratory findings revealed parathyroid hormone (PTH)-dependent hypercalcemia (total calcium = 14.3 mg/dL and PTH = 1,573 pg/mL), a nodular lesion in the upper pole of the left thyroid lobe and increased uptake in left upper cervical region. The patient underwent left superior parathyroidectomy in September 2011, which led to the normalization of hypercalcemia and regression of the orbital tumor, as seen on control CT scan. This case highlights the spontaneous regression of the brown tumor after surgical management of the parathyroid adenoma.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972015000500455&lng=en&tlng=en
collection DOAJ
language English
format Article
sources DOAJ
author Felipe Martins de Oliveira
Tiago Eidy Makimoto
Nilza Maria Scalissi
Marília Martins Silveira Marone
Sergio Setsuo Maeda
spellingShingle Felipe Martins de Oliveira
Tiago Eidy Makimoto
Nilza Maria Scalissi
Marília Martins Silveira Marone
Sergio Setsuo Maeda
Regression of orbital brown tumor after surgical removal of parathyroid adenoma
Archives of Endocrinology and Metabolism
author_facet Felipe Martins de Oliveira
Tiago Eidy Makimoto
Nilza Maria Scalissi
Marília Martins Silveira Marone
Sergio Setsuo Maeda
author_sort Felipe Martins de Oliveira
title Regression of orbital brown tumor after surgical removal of parathyroid adenoma
title_short Regression of orbital brown tumor after surgical removal of parathyroid adenoma
title_full Regression of orbital brown tumor after surgical removal of parathyroid adenoma
title_fullStr Regression of orbital brown tumor after surgical removal of parathyroid adenoma
title_full_unstemmed Regression of orbital brown tumor after surgical removal of parathyroid adenoma
title_sort regression of orbital brown tumor after surgical removal of parathyroid adenoma
publisher Brazilian Society of Endocrinology and Metabolism
series Archives of Endocrinology and Metabolism
issn 2359-4292
publishDate 2015-08-01
description Brown tumors are rare skeletal manifestations that occur in less than 2% of primary hyperparathyroidism (PHPT) cases. Even rarer is the occurrence of brown tumor of the orbit, and few cases have been reported around the world. The rare instance of this benign tumor has prompted us to report the case and treatment of an orbital brown tumor in a patient with PHPT caused by parathyroid adenoma. We present the case of a patient undergoing follow-up at a referral center. The 60-year-old female patient, presented herself with progressive swelling in the nasal region, epistaxis and proptosis, she had noticed seven months prior to our examination. Multiple imaging and laboratory findings revealed parathyroid hormone (PTH)-dependent hypercalcemia (total calcium = 14.3 mg/dL and PTH = 1,573 pg/mL), a nodular lesion in the upper pole of the left thyroid lobe and increased uptake in left upper cervical region. The patient underwent left superior parathyroidectomy in September 2011, which led to the normalization of hypercalcemia and regression of the orbital tumor, as seen on control CT scan. This case highlights the spontaneous regression of the brown tumor after surgical management of the parathyroid adenoma.
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S2359-39972015000500455&lng=en&tlng=en
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