A Rare Case of Cherubism In a 23-Year-Old Man

Background and Objectives:  Cherubism is a rare hereditary autosomal dominant fibro-osseous disease that is characterized by painless, bilateral, symmetric swelling in the jaw with multilocular radiolucent lesions in the maxilla, mandible, or both, and give the patient a typical “cherubic” appearanc...

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Main Authors: Arezoo Heidary, Mohammadhasan Akhavankarbasi, Yasaman Sabaghzadgan, Ehsan Babaie
Format: Article
Language:fas
Published: Qom University of Medical Sciences 2022-08-01
Series:Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum
Subjects:
Online Access:http://journal.muq.ac.ir/article-1-3506-en.html
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author Arezoo Heidary
Mohammadhasan Akhavankarbasi
Yasaman Sabaghzadgan
Ehsan Babaie
author_facet Arezoo Heidary
Mohammadhasan Akhavankarbasi
Yasaman Sabaghzadgan
Ehsan Babaie
author_sort Arezoo Heidary
collection DOAJ
description Background and Objectives:  Cherubism is a rare hereditary autosomal dominant fibro-osseous disease that is characterized by painless, bilateral, symmetric swelling in the jaw with multilocular radiolucent lesions in the maxilla, mandible, or both, and give the patient a typical “cherubic” appearance. It occurs in children, especially boys, aged 2-5 years. The aim of this study was to report a case of cherubism at an uncommon age that did not improve with age. Case Presentation: The patient was a 23-year-old man complaining of bilateral jaw pain along with swelling and multiple bilateral radiolucent lesions with a previous history of childhood cherubism. In the examination, bilateral and symmetric swelling of the face, especially in the maxilla region, with eyes raised to heaven were evident. The pain was more in the vicinity of the condyle. No abnormal manifestations were observed by the intraoral examination. In the radiographic view, multiple bilateral and symmetric lucent lesions were observed on trunk and mandible, continued to the neck of the condyle. Conclusion: Despite the common manifestations and age in patients, cherubism can show different manifestations; lack of attention to the patient’s history can lead to misdiagnosis by the pathologist and unnecessary treatments. Due to being a self-limiting condition, non-invasive treatments are preferred; however, surgical management is sometimes required for cosmetic reasons.
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spelling doaj.art-037190639c564450bf89a9d811a12bc02023-02-22T05:41:26ZfasQom University of Medical SciencesMajallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum1735-77992008-13752022-08-01165430439A Rare Case of Cherubism In a 23-Year-Old ManArezoo Heidary0Mohammadhasan Akhavankarbasi1Yasaman Sabaghzadgan2Ehsan Babaie3 Department of Oral and Maxillofacial Medicine, School of Dentistry, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Department of Oral and Maxillofacial Medicine, School of Dentistry, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Department of Oral and Maxillofacial Medicine, School of Dentistry, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Department of Oral and Maxillofacial Medicine, School of Dentistry, Shahid Sadoughi University of Medical Sciences, Yazd, Iran. Background and Objectives:  Cherubism is a rare hereditary autosomal dominant fibro-osseous disease that is characterized by painless, bilateral, symmetric swelling in the jaw with multilocular radiolucent lesions in the maxilla, mandible, or both, and give the patient a typical “cherubic” appearance. It occurs in children, especially boys, aged 2-5 years. The aim of this study was to report a case of cherubism at an uncommon age that did not improve with age. Case Presentation: The patient was a 23-year-old man complaining of bilateral jaw pain along with swelling and multiple bilateral radiolucent lesions with a previous history of childhood cherubism. In the examination, bilateral and symmetric swelling of the face, especially in the maxilla region, with eyes raised to heaven were evident. The pain was more in the vicinity of the condyle. No abnormal manifestations were observed by the intraoral examination. In the radiographic view, multiple bilateral and symmetric lucent lesions were observed on trunk and mandible, continued to the neck of the condyle. Conclusion: Despite the common manifestations and age in patients, cherubism can show different manifestations; lack of attention to the patient’s history can lead to misdiagnosis by the pathologist and unnecessary treatments. Due to being a self-limiting condition, non-invasive treatments are preferred; however, surgical management is sometimes required for cosmetic reasons.http://journal.muq.ac.ir/article-1-3506-en.htmlcherubismfibrous dysplasia of bonemandible
spellingShingle Arezoo Heidary
Mohammadhasan Akhavankarbasi
Yasaman Sabaghzadgan
Ehsan Babaie
A Rare Case of Cherubism In a 23-Year-Old Man
Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum
cherubism
fibrous dysplasia of bone
mandible
title A Rare Case of Cherubism In a 23-Year-Old Man
title_full A Rare Case of Cherubism In a 23-Year-Old Man
title_fullStr A Rare Case of Cherubism In a 23-Year-Old Man
title_full_unstemmed A Rare Case of Cherubism In a 23-Year-Old Man
title_short A Rare Case of Cherubism In a 23-Year-Old Man
title_sort rare case of cherubism in a 23 year old man
topic cherubism
fibrous dysplasia of bone
mandible
url http://journal.muq.ac.ir/article-1-3506-en.html
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