Craniofacial fibrous dysplasia mimicking sinunasal mucocele: Case report

Rimande U.Joel, Rosethe Rimande-Joel, Eyo O.Ekpenyong, Joseph I.Kuni, Millicent O. Obajimi
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Abstract

Background: Fibrous Dysplasia is a congenital, non-inherited, benign intra-medullary bone lesion in which the normal bone marrow is replaced by abnormal fibro-osseous tissue. It can manifest in axial and extra -axial skeleton and tissues. The wide range of clinical manifestations from skeletal changes to soft tissues swellings and skin discoloration makes it a disease of note in the clinical settings. Some of its complications include malignant transformation, gastrointestinal reflux to cardiac involvement with arrhythmias and even sudden death. Until recently with advent of modern imaging modalities, it was a disease of diagnostic debacle as it was often misdiagnosed .This is a case report of a 17 year old male who was misdiagnosed as sinunasal mucocele until histology proved it to be fibrous dysplasia. Objective: The objective of the report is to draw attention to the diagnostic challenge posed at CT imaging. Methods: This case report was carried out at University College Hospital Ibadan. Results: Showed right sided facial swelling measuring about 15x10cm. The mass was firm to hard in consistency, non-tender and not attached to the overlying skin. There was no loss of sensation in the skin over it. The right eye was displaced superiorly and laterally. A nasal aspect of the mass was seen to occupy the whole of the ipsilateral nasal cavity which it occluded deviating the nasal septum to the left and narrowing the left nasal cavity. It was fleshy and showed contact bleeding. The attending ENT Surgeons made a working diagnosis of right sinunasal tumour with possible malignant transformation. The radiographs of the sinuses showed expansile sclerotic lesion involving the nasal bones, the right maxillary bone, right ethmoidal and maxillary sinuses. The inferior aspect of the right frontal sinus was also affected. A cranial computed tomography (CT) scan (Fig 2-4) showed a multi-loculated hypodense mass with mildly enhancing septations (HU16) within the right frontal, ethmoidal, sphenoidal and maxillary sinuses. There was associated expansion of the affected sinuses with thinning of their cortices. No evidence of aggressive bony destruction was seen. The radiologists made a diagnosis of benign sinunasal tumour most likely mucocele. After right maxillectomy, histology proved the lesion to be fibrous dysplasia. This report goes further to support the need for application of more imaging modalities especially the modern and higher slices CT scanner, higher Tesla(2T )MRI , PET and fusion CT/PET scanners in arriving at radiological diagnosis that will be more compatible with the pathological condition of the patients as against what was in place at the time of this case report .Radiologists are also encouraged to have a high index of suspicion for the disease and to explore the possibilities of the differentials in order not to miss the diagnosis of FD
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模拟鼻窦黏液囊肿的颅面纤维发育不良1例
背景:纤维性发育不良是一种先天性、非遗传性、良性髓内骨病变,正常骨髓被异常纤维骨组织所取代。它可以表现在轴向和轴外的骨骼和组织。从骨骼变化到软组织肿胀和皮肤变色的广泛临床表现使其成为临床环境中值得注意的疾病。它的一些并发症包括恶性转化,胃肠道反流累及心脏并心律失常,甚至猝死。本文报告一位17岁男性患者,曾被误诊为鼻窦黏液囊肿,经组织学证实为纤维性发育不良。目的:本报告的目的是引起人们对CT成像诊断挑战的关注。方法:本病例在伊巴丹大学附属医院进行。结果:右侧面部肿胀约15x10cm。肿块坚固坚硬,不柔软,不附着于上覆皮肤。它上面的皮肤没有失去知觉。右眼上外侧移位。肿块的鼻部部分被发现占据了整个同侧鼻腔,它阻塞了鼻中隔向左偏,使左鼻腔变窄。是肉质的,有接触性出血。主治耳鼻喉外科医生诊断为右鼻窦肿瘤,可能有恶性转化。鼻窦x线片显示扩张性硬化病变累及鼻骨、右上颌骨、右筛窦及上颌窦。右额窦的下侧面也受到影响。颅脑计算机断层扫描(图2-4)显示右侧额窦、筛窦、蝶窦和上颌窦内有多室低密度肿块,分隔轻度增强(HU16)。伴有受累鼻窦扩张和鼻窦皮层变薄。未见侵袭性骨质破坏的证据。放射科医生诊断为良性鼻窦肿瘤,极有可能是粘液囊肿。右上颌切除术后,组织学证实病变为纤维性发育不良。该报告进一步支持应用更多成像方式的需求,特别是现代和更高的切片CT扫描仪,更高的特斯拉(2T)MRI,PET和融合CT/PET扫描仪在达到放射诊断时将更符合患者的病理状况,而不是在本病例报告时的情况。放射科医生也被鼓励对疾病有高度的怀疑指数,并探索鉴别的可能性,以避免错过FD的诊断
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