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Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report
RATIONALE: Only 4.5% of brown tumors involve facial bones; of these, solitary bone involvement is usual. Brown tumors of multiple facial bones are extremely rare. Here, we report the case of a brown tumor of multiple facial bones initially misdiagnosed as an odontogenic cyst. PATIENT CONCERNS: A pre...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Wolters Kluwer Health
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112971/ https://www.ncbi.nlm.nih.gov/pubmed/30113484 http://dx.doi.org/10.1097/MD.0000000000011877 |
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author | Zou, Haixiao Song, Li Jia, Mengqi Wang, Li Sun, Yanfang |
author_facet | Zou, Haixiao Song, Li Jia, Mengqi Wang, Li Sun, Yanfang |
author_sort | Zou, Haixiao |
collection | PubMed |
description | RATIONALE: Only 4.5% of brown tumors involve facial bones; of these, solitary bone involvement is usual. Brown tumors of multiple facial bones are extremely rare. Here, we report the case of a brown tumor of multiple facial bones initially misdiagnosed as an odontogenic cyst. PATIENT CONCERNS: A pregnant 26-year-old woman was referred to our hospital with painful swelling of multiple facial bones, anemia, urinary calculi, marasmus, and a history of multiple bone fractures. Laboratory examination revealed an elevated serum calcium level of 3.09 mmol/L (normal range: 2.0–2.8 mmol/L) and a low phosphorus level of 0.62 mmol/L (normal range: 0.81–1.65 mmol/L). The serum alkaline phosphatase concentration was 397 IU/L (normal range: 24–82 IU/L) and parathyroid hormone level was 267 pg/mL (normal range: 14–72 pg/mL). Cone beam computed tomography revealed multiple ossifying fibromas of the maxilla and mandible. Incisional biopsy revealed abundant spindle cells with areas of hemorrhage and haphazardly arranged diffuse multinucleated giant cells. DIAGNOSES: The patient was diagnosed with primary hyperparathyroidism (HPT). INTERVENTIONS: She was treated by parathyroidectomy. OUTCOMES: The multiple osteitis fibrosa cystica gradually resolved as bone re-mineralized. The patient has been followed up for 2 years without evidence of tumor recurrence. LESSONS: As multiple osteolytic lesions of facial bones can be caused by primary HPT, serum calcium and parathyroid hormone assays should be performed routinely when investigating these lesions. |
format | Online Article Text |
id | pubmed-6112971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-61129712018-09-07 Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report Zou, Haixiao Song, Li Jia, Mengqi Wang, Li Sun, Yanfang Medicine (Baltimore) Research Article RATIONALE: Only 4.5% of brown tumors involve facial bones; of these, solitary bone involvement is usual. Brown tumors of multiple facial bones are extremely rare. Here, we report the case of a brown tumor of multiple facial bones initially misdiagnosed as an odontogenic cyst. PATIENT CONCERNS: A pregnant 26-year-old woman was referred to our hospital with painful swelling of multiple facial bones, anemia, urinary calculi, marasmus, and a history of multiple bone fractures. Laboratory examination revealed an elevated serum calcium level of 3.09 mmol/L (normal range: 2.0–2.8 mmol/L) and a low phosphorus level of 0.62 mmol/L (normal range: 0.81–1.65 mmol/L). The serum alkaline phosphatase concentration was 397 IU/L (normal range: 24–82 IU/L) and parathyroid hormone level was 267 pg/mL (normal range: 14–72 pg/mL). Cone beam computed tomography revealed multiple ossifying fibromas of the maxilla and mandible. Incisional biopsy revealed abundant spindle cells with areas of hemorrhage and haphazardly arranged diffuse multinucleated giant cells. DIAGNOSES: The patient was diagnosed with primary hyperparathyroidism (HPT). INTERVENTIONS: She was treated by parathyroidectomy. OUTCOMES: The multiple osteitis fibrosa cystica gradually resolved as bone re-mineralized. The patient has been followed up for 2 years without evidence of tumor recurrence. LESSONS: As multiple osteolytic lesions of facial bones can be caused by primary HPT, serum calcium and parathyroid hormone assays should be performed routinely when investigating these lesions. Wolters Kluwer Health 2018-08-17 /pmc/articles/PMC6112971/ /pubmed/30113484 http://dx.doi.org/10.1097/MD.0000000000011877 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Research Article Zou, Haixiao Song, Li Jia, Mengqi Wang, Li Sun, Yanfang Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report |
title | Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report |
title_full | Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report |
title_fullStr | Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report |
title_full_unstemmed | Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report |
title_short | Brown tumor of multiple facial bones associated with primary hyperparathyroidism: A clinical case report |
title_sort | brown tumor of multiple facial bones associated with primary hyperparathyroidism: a clinical case report |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6112971/ https://www.ncbi.nlm.nih.gov/pubmed/30113484 http://dx.doi.org/10.1097/MD.0000000000011877 |
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