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Psammomatoid Ossifying Fibroma of the Ethmoid Sinus with Secondary Intracranial Aneurymal Bone Cyst: A Case Report and Literature Review

机译:筛窦类筛窦骨化性纤维化伴颅内继发性动脉瘤性骨囊肿:一例报告并文献复习

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摘要

Juvenile psammomatoid ossifying fibroma (JPOF) is a rare, slowly progressive tumor of the extragnathic craniofacial bones, with a tendency toward locally aggressive behavior and recurrence. The pathognomonic histopathologic feature is the presence of spherical ossicles, which are similar to psammoma bodies. Very few cases in association with secondary aneurysmal bone cyst (ABC) formation have been reported in literature. Treatment consists of complete surgical removal. However, incomplete excision has been associated with a high local recurrence rate. The prognosis is good because malignant change and metastasis have not been reported. The authors are reporting a case of JPOF of the ethmoid bones with secondary ABC in a 7-year-old female patient.
机译:幼年类滑膜僵化性纤维瘤(JPOF)是一种罕见的缓慢发展的颅外颅面骨肿瘤,具有局部侵袭性行为和复发的趋势。病理人文学的组织病理学特征是球形小骨的存在,类似于肺腺瘤体。文献报道很少有继发性动脉瘤性骨囊肿(ABC)形成的病例。治疗包括彻底的手术切除。然而,不完全切除与高局部复发率相关。由于尚未报告恶性变化和转移,因此预后良好。作者报告了一名7岁女性患者中伴有ABC的筛骨筛查JPOF的病例。

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