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Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report

A 19-year-old woman presented with swelling of the left forehead without pain. She did not have any relevant past or family history. Computed tomography showed destruction of the outer cortex of the frontal bone. A solitary mass lesion with a fluid collection was detected with magnetic resonance ima...

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Autores principales: Koketsu, Yuta, Tanei, Takafumi, Kuwabara, Kyoko, Hasegawa, Toshinori, Kato, Takenori, Maesawa, Satoshi, Nishimura, Yusuke, Araki, Yoshio, Saito, Ryuta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nagoya University 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281851/
https://www.ncbi.nlm.nih.gov/pubmed/37346833
http://dx.doi.org/10.18999/nagjms.85.2.395
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author Koketsu, Yuta
Tanei, Takafumi
Kuwabara, Kyoko
Hasegawa, Toshinori
Kato, Takenori
Maesawa, Satoshi
Nishimura, Yusuke
Araki, Yoshio
Saito, Ryuta
author_facet Koketsu, Yuta
Tanei, Takafumi
Kuwabara, Kyoko
Hasegawa, Toshinori
Kato, Takenori
Maesawa, Satoshi
Nishimura, Yusuke
Araki, Yoshio
Saito, Ryuta
author_sort Koketsu, Yuta
collection PubMed
description A 19-year-old woman presented with swelling of the left forehead without pain. She did not have any relevant past or family history. Computed tomography showed destruction of the outer cortex of the frontal bone. A solitary mass lesion with a fluid collection was detected with magnetic resonance imaging. Because the swelling of the left forehead had enlarged rapidly with osteolytic changes, surgical removal of the lesion was performed. The lesion appeared to be enveloped in a fibrous capsule. The soft lesion was removed from the frontal bone. The outer frontal bone was absent, although the inner frontal bone was preserved. Then, the frontal bone was resected with margins from the edge of the erosion. The dura mater under the lesion was intact. A cranioplasty was performed using titanium mesh. On histological examination, the trabecular bones revealed irregular shapes and arrangements, indicating fibrous dysplasia. There was a continuous high-cell-concentration pathological lesion outside the fibrous dysplasia. There were numerous cells, such as mononuclear cells, osteoclast-like multinucleated giant cells, foam cells, and red blood cells. The osteoclast-like multinucleated giant cells and other cells did not show significant nuclear atypia. Immunostaining with H3.3G34W was negative, and the ubiquitin-specific peptidase 6/Tre-2 gene showed no rearrangements. The histopathological diagnosis was secondary aneurysmal bone cyst with fibrous dysplasia. Additional postsurgical therapy was not performed. There has been no evidence of recurrence of the lesion for two years.
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spelling pubmed-102818512023-06-21 Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report Koketsu, Yuta Tanei, Takafumi Kuwabara, Kyoko Hasegawa, Toshinori Kato, Takenori Maesawa, Satoshi Nishimura, Yusuke Araki, Yoshio Saito, Ryuta Nagoya J Med Sci Case Report A 19-year-old woman presented with swelling of the left forehead without pain. She did not have any relevant past or family history. Computed tomography showed destruction of the outer cortex of the frontal bone. A solitary mass lesion with a fluid collection was detected with magnetic resonance imaging. Because the swelling of the left forehead had enlarged rapidly with osteolytic changes, surgical removal of the lesion was performed. The lesion appeared to be enveloped in a fibrous capsule. The soft lesion was removed from the frontal bone. The outer frontal bone was absent, although the inner frontal bone was preserved. Then, the frontal bone was resected with margins from the edge of the erosion. The dura mater under the lesion was intact. A cranioplasty was performed using titanium mesh. On histological examination, the trabecular bones revealed irregular shapes and arrangements, indicating fibrous dysplasia. There was a continuous high-cell-concentration pathological lesion outside the fibrous dysplasia. There were numerous cells, such as mononuclear cells, osteoclast-like multinucleated giant cells, foam cells, and red blood cells. The osteoclast-like multinucleated giant cells and other cells did not show significant nuclear atypia. Immunostaining with H3.3G34W was negative, and the ubiquitin-specific peptidase 6/Tre-2 gene showed no rearrangements. The histopathological diagnosis was secondary aneurysmal bone cyst with fibrous dysplasia. Additional postsurgical therapy was not performed. There has been no evidence of recurrence of the lesion for two years. Nagoya University 2023-05 /pmc/articles/PMC10281851/ /pubmed/37346833 http://dx.doi.org/10.18999/nagjms.85.2.395 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ).
spellingShingle Case Report
Koketsu, Yuta
Tanei, Takafumi
Kuwabara, Kyoko
Hasegawa, Toshinori
Kato, Takenori
Maesawa, Satoshi
Nishimura, Yusuke
Araki, Yoshio
Saito, Ryuta
Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
title Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
title_full Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
title_fullStr Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
title_full_unstemmed Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
title_short Secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
title_sort secondary aneurysmal bone cyst of the frontal bone with fibrous dysplasia showing rapid expansion: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10281851/
https://www.ncbi.nlm.nih.gov/pubmed/37346833
http://dx.doi.org/10.18999/nagjms.85.2.395
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