Primary sclerosing fibroinflammatory pseudotumor of the maxillary sinus misdiagnosed as migraine: A case report

Q3 Dentistry
Safwan Salih, Sadeq Qanah, Fadi Nahhab
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引用次数: 0

Abstract

The head and neck region is a complex anatomical area where overlapping structures and nonspecific symptoms often make accurate diagnosis challenging. Facial pain, in particular, is a common yet ambiguous symptom frequently attributed to prevalent conditions like migraine, which can delay recognition of less common but clinically significant diseases. One such condition is Primary Sclerosing Fibroinflammatory Pseudotumor—a rare, benign lesion that can mimic malignancy both clinically and radiologically.We present the case of an 18-year-old female with chronic facial pain and globe displacement, misdiagnosed as migraine for four years. Imaging revealed a mass in the maxillary sinus with bone erosion and orbital involvement. A core needle biopsy was inconclusive, and definitive diagnosis was achieved only after surgical excision. Histopathological and immunohistochemical analysis confirmed Primary Sclerosing Fibroinflammatory Pseudotumor. The patient experienced substantial clinical improvement following combined surgical and corticosteroid therapy. This case highlights the importance of including rare pathologies in the differential diagnosis of maxillofacial masses and demonstrates the value of thorough investigation when symptoms persist despite standard treatment.
上颌窦原发性硬化性纤维炎性假瘤误诊为偏头痛1例
头颈部是一个复杂的解剖区域,其中重叠的结构和非特异性症状往往使准确诊断具有挑战性。尤其是面部疼痛,是一种常见但模棱两可的症状,通常归因于偏头痛等常见疾病,这可能会延迟对不太常见但具有临床意义的疾病的识别。其中一种情况是原发性硬化性纤维炎性假瘤,这是一种罕见的良性病变,在临床和放射学上都能模仿恶性肿瘤。我们提出的情况下,18岁的女性慢性面部疼痛和全球位移,误诊为偏头痛四年。影像学显示上颌窦肿块伴骨侵蚀及眼眶受累。核心穿刺活检不确定,只有在手术切除后才得到明确诊断。组织病理学和免疫组化分析证实原发性硬化性纤维炎性假瘤。在手术和皮质类固醇联合治疗后,患者的临床状况得到了显著改善。本病例强调了在颌面部肿块鉴别诊断中包括罕见病理的重要性,并证明了在标准治疗后症状仍然存在时进行彻底检查的价值。
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来源期刊
Oral and Maxillofacial Surgery Cases
Oral and Maxillofacial Surgery Cases Medicine-Otorhinolaryngology
CiteScore
0.60
自引率
0.00%
发文量
43
审稿时长
69 days
期刊介绍: Oral and Maxillofacial Surgery Cases is a surgical journal dedicated to publishing case reports and case series only which must be original, educational, rare conditions or findings, or clinically interesting to an international audience of surgeons and clinicians. Case series can be prospective or retrospective and examine the outcomes of management or mechanisms in more than one patient. Case reports may include new or modified methodology and treatment, uncommon findings, and mechanisms. All case reports and case series will be peer reviewed for acceptance for publication in the Journal.
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