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远外侧额窦纤维组织细胞瘤——罕见病例观察

Fibrous Histiocytoma in the Far Lateral Frontal Sinus-A Rare Observation.

作者信息

Wilhelmer Alexander, Kiss Peter, Habenbacher Michael, Brčić Luka, Andrianakis Alexandros

机构信息

Department of Otorhinolaryngology, Medical University of Graz, Auenbruggerplatz 26, 8010 Graz, Austria.

Diagnostic and Research Institute of Pathology, Medical University of Graz, Auenbruggerplatz 26, 8010 Graz, Austria.

出版信息

Diagnostics (Basel). 2024 Dec 28;15(1):56. doi: 10.3390/diagnostics15010056.

Abstract

This report describes a rare occurrence of benign fibrous histiocytoma in the frontal sinus of a 38-year-old male. The patient presented with acute symptoms, including sudden-onset headache, nausea, and general discomfort, although neurological, otorhinolaryngological and laboratory examinations showed no abnormalities. A cranial CT scan revealed a cystic, osteodestructive lesion measuring 2.5 cm in the far lateral right frontal sinus, initially suspected to be a mucocele due to radiological characteristics and the patient's history of recurring frontal headaches and retrobulbar pressure. Elective surgical excision was performed via an external supraorbital approach due to the lesion's lateral location. Histopathological examination of the excised tissue revealed characteristic features of benign fibrous histiocytoma, including spindle cell proliferation and the presence of histiocytes and siderophages. Immunohistochemistry further supported the diagnosis, showing EMA, S100, and creatinine negativity with SMA positivity. This case is unique, as it represents the first reported benign fibrous histiocytoma in the frontal sinus. During regular follow-up, the patient remained symptom-free and showed no recurrence. This report underscores the importance of considering rare diagnoses for cystic skull lesions and supports tailored surgical approaches based on lesion location.

摘要

本报告描述了一名38岁男性额窦罕见的良性纤维组织细胞瘤病例。患者出现急性症状,包括突发头痛、恶心和全身不适,尽管神经学、耳鼻喉科及实验室检查均未发现异常。头颅CT扫描显示右额窦最外侧有一个2.5厘米的囊性骨质破坏病变,由于影像学特征以及患者反复出现额部头痛和球后压迫的病史,最初怀疑是黏液囊肿。由于病变位于外侧,通过眶上外侧入路进行了择期手术切除。切除组织的组织病理学检查显示出良性纤维组织细胞瘤的特征性表现,包括梭形细胞增殖以及组织细胞和含铁血黄素巨噬细胞的存在。免疫组织化学进一步支持了诊断,显示上皮膜抗原(EMA)、S100和肌酸酐阴性,平滑肌肌动蛋白(SMA)阳性。该病例具有独特性,因为它是首次报道的额窦良性纤维组织细胞瘤。在定期随访中,患者无症状,未出现复发。本报告强调了对于囊性颅骨病变考虑罕见诊断的重要性,并支持基于病变位置的个性化手术方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef7c/11719909/7e50f1d94376/diagnostics-15-00056-g001.jpg

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