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顶骨促结缔组织增生性(胶原性)纤维瘤:病例报告及文献复习

Desmoplastic (collagenous) fibroma of the parietal bone: Case report and review of the literature.

作者信息

Zhang Baolong, Yu Haiyan, Pylypenko Dmytro, Sun Jining

机构信息

Department of Radiology, Weifang Maternal and Child Health Hospital, Weifang, China.

Department of Radiology, Weifang People's Hospital, Weifang, China.

出版信息

J Clin Imaging Sci. 2024 Dec 10;14:48. doi: 10.25259/JCIS_136_2024. eCollection 2024.

Abstract

Desmoplastic fibroma (DF) is an uncommon benign bone tumor that typically affects the facial bones, with cerebral cranium involvement being extremely rare. We report a unique case of DF in the parietal bone of a 28-year-old woman, notable for its rapid growth during pregnancy-a phenomenon not previously documented. The imaging features of this case also differ from all but one previously reported case. The patient underwent surgical removal, and histopathology confirmed the diagnosis of DF (collagenous fibroma). After 17 months of follow-up, no local recurrence was observed. We also provide a comprehensive review of 32 cases involving DF of the cerebral cranium, analyzing clinical features, imaging findings, treatment methods, and recurrence patterns. This case highlights the importance of considering DF in the differential diagnosis of cranial lesions, particularly in pregnant patients with rapid tumor growth. Complete surgical resection with a wide margin remains the recommended treatment to minimize recurrence risk.

摘要

促结缔组织增生性纤维瘤(DF)是一种罕见的良性骨肿瘤,通常累及面骨,累及脑颅骨极为罕见。我们报告了一例独特的DF病例,发生于一名28岁女性的顶骨,其在孕期生长迅速,这一现象此前未见报道。该病例的影像学特征也与之前报道的所有病例(仅有一例除外)不同。患者接受了手术切除,组织病理学确诊为DF(胶原性纤维瘤)。随访17个月后,未观察到局部复发。我们还对32例累及脑颅骨的DF病例进行了全面综述,分析了临床特征、影像学表现、治疗方法及复发模式。该病例凸显了在颅骨病变的鉴别诊断中考虑DF的重要性,尤其是在肿瘤生长迅速的孕妇中。广泛切缘的完整手术切除仍是降低复发风险的推荐治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf4f/11704291/2c3a04fd8bdb/JCIS-14-48-g001.jpg

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