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青少年骨化性纤维瘤的砂粒体型变种

Psammomatoid variant of juvenile ossifying fibroma.

作者信息

Aslan Figen, Yazici Hasmet, Altun Eren

机构信息

Department of Pathology, School of Medicine, Balikesir University, Balikesir, Turkey.

Department of Otolaryngology, School of Medicine, Balikesir University, Balikesir, Turkey.

出版信息

Indian J Pathol Microbiol. 2018 Jul-Sep;61(3):443-445. doi: 10.4103/IJPM.IJPM_577_17.

Abstract

Juvenile ossifying fibroma (JOF) is a rare benign tumor of the craniofacial bones differing from other fibro-osseous lesions in terms of early age of onset, aggressive clinical behavior, and high recurrence rate. Histopathologically, it is divided into two as trabecular JOF (TrJOF) and psammomatoid JOF (PsJOF). In PsJOF, psammoma-like spherical ossicles constitute pathognomonic histopathological images, whereas TrJOF has trabeculae of fibrillary osteoid and woven bone. Despite the histopathologic separation, both lesions have similar clinical behavior, thus the treatment procedure is also the same. Complete surgical resection is preferred for the treatment. We report a rare case of PsJOF involving the maxillary sinus and resultant facial symmetry in a 13-year-old female child.

摘要

青少年骨化性纤维瘤(JOF)是一种罕见的颅面骨良性肿瘤,在发病年龄、临床侵袭性行为和高复发率方面与其他纤维骨性病变不同。组织病理学上,它分为小梁状青少年骨化性纤维瘤(TrJOF)和砂粒样青少年骨化性纤维瘤(PsJOF)两种。在砂粒样青少年骨化性纤维瘤中,砂粒体样球形小骨构成了特征性的组织病理学图像,而小梁状青少年骨化性纤维瘤则有纤维性类骨质和编织骨小梁。尽管在组织病理学上有所区分,但这两种病变具有相似的临床行为,因此治疗方法也相同。治疗首选完整的手术切除。我们报告了一例罕见的砂粒样青少年骨化性纤维瘤累及上颌窦并导致一名13岁女童面部不对称的病例。

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