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

IF 0.9 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Nagoya Journal of Medical Science Pub Date : 2023-05-01 DOI:10.18999/nagjms.85.2.395
Yuta Koketsu, Takafumi Tanei, Kyoko Kuwabara, Toshinori Hasegawa, Takenori Kato, Satoshi Maesawa, Yusuke Nishimura, Yoshio Araki, Ryuta Saito
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引用次数: 1

Abstract

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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继发性额骨动脉瘤性骨囊肿伴纤维发育不良,迅速扩张1例。
19岁女性,左前额肿胀,无疼痛。她没有任何相关的过去或家族史。计算机断层扫描显示额骨外皮层受损。磁共振成像发现孤立肿块病变伴积液。由于左前额肿胀迅速扩大并伴有溶骨改变,手术切除病变。病灶被纤维囊包裹。从额骨上取出软组织病变。外额骨不见了,但内额骨保留了下来。然后,从侵蚀的边缘切除额骨。病变下的硬脑膜完好。采用钛网进行颅骨成形术。组织学检查显示骨小梁形状和排列不规则,提示纤维发育不良。纤维发育不良外可见连续的高细胞浓度病变。细胞数量较多,如单核细胞、破骨细胞样多核巨细胞、泡沫细胞、红细胞等。破骨细胞样多核巨细胞及其他细胞未见明显的核异型性。H3.3G34W免疫染色阴性,泛素特异性肽酶6/ tre2基因未见重排。组织病理学诊断为继发性动脉瘤样骨囊肿伴纤维发育不良。未进行额外的术后治疗。两年来没有发现病变复发的迹象。
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来源期刊
Nagoya Journal of Medical Science
Nagoya Journal of Medical Science MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
1.30
自引率
0.00%
发文量
65
审稿时长
>12 weeks
期刊介绍: The Journal publishes original papers in the areas of medical science and its related fields. Reviews, symposium reports, short communications, notes, case reports, hypothesis papers, medical image at a glance, video and announcements are also accepted. Manuscripts should be in English. It is recommended that an English check of the manuscript by a competent and knowledgeable native speaker be completed before submission.
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