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Diaphragmatic Schwannoma Mimicking Hydatid Cyst Depicted by FDG PET/CT

机译:用FDG PET / CT描绘肌肉瘤样包虫囊肿

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Schwannoma is generally a benign, slow-growing, encapsulated tumor originating from the nerve sheath most commonly located in the head and neck regions and extremities. Present study aimed to report FDG PET/CT findings of an extraordinary located schwannoma arising from the right diaphragm. Thoracic CT of a 39-year-old male showed an encapsulated, well-defined round, heterogenous cystic lesion on the right hemithorax which was falsely diagnosed as a hydatid cyst. FDG PET/CT was requested for the metabolic characterization of this mass and revealed mild to moderate hypermetabolism at the solid components of this lesion. Surgical excision was performed and histological examination revealed schwannoma. INTRODUCTION Schwannoma is a benign tumor that originates from the Schwann cells surrounding peripheral and cranial nerves. It has a predilection for the head and neck and ?exor surfaces of the upper and lower extremities (1).Schwannoma most frequently present in patients aged 20 to 50 years, more frequently in men than in women (2). They comprise 5% of all benign soft tissue tumours (3). Schwannoma of the chest wall and diaphragm are rare. Schwannoma is often found incidentally or present with vague, non-speci?c symptoms. This benign tumor is almost invariably slow growing, non-aggressive neoplasm and it is solitary in the vast majority of cases. Of 5% to 18% schwannomas are associated with neuro?bromatosis type I (4), in which case lesions may be multiple and often plexiform. Malignant transformation is very rare. On gross appearance, schwannoma is usually seen as solitary, well circumscribed, encapsulated lesion (5). The definitive diagnosis remains histologic. Histologically, typical schwannomas are composed of intermixed Antoni A components (cellular and arranged in short bundles or interlacing fascicles) and Antoni B areas (less cellular and organized with more myxoid components). The cellular variant (which includes most large retroperitoneal and pelvic schwannomas) has a uniform spindle cell appearance without Antoni A or B areas. Characteristically, all schwannomas show uniform and intense staining for S100 protein (6). It is important for the radiologist to consider the diagnosis of benign schwannoma when presented with a retroperitoneal or pelvic mass, to avoid unnecessary surgery, because these lesions can be managed conservatively (3). In this case report we aimed to report FDG PET/CT findings of an extraordinary located schwannoma arising from the right diaphragm. CASE REPORT A 39-year-old man suffered from cough and sputum was referred to the outpatient clinic of chest medicine. Diagnostic computed tomography (CT) was performed. It showed encapsulated, well-defined, round, heteregenous cystic soft tissue mass that arised from the right diaphragm. The lesion was measured approximately 10 cm in diameter and extended from right dome of the diaphragm to superior pole of the right kidney. Since Turkey is an endemic country for Echinococcus infestation, it was initially misdiagnosed as a hydatid cyst according to its CT pattern. F-18 flourodeoxyglucose (FDG)PET/CT was requested to exclude possible malignancy. (A) Axial, (B) coronal, (C) saggital PET, CT and combined PET/CT images demonstrated mild to moderate FDG uptake [maximum standardized uptake values (SUVmax): 4,1] at the solid components which were located in the peripheral and central zones of this cystic lesion.The total resection was perfomed and histological examination revealed a benign schwannoma.
机译:神经鞘瘤通常是一种良性的,生长缓慢的,包囊的肿瘤,起源于神经鞘,最常见于头颈部区域和四肢。本研究旨在报告FDG PET / CT发现的由右隔膜引起的异常定位的神经鞘瘤。一名39岁男性的胸腔CT显示右半胸囊囊肿,轮廓分明,圆形,异质囊性病变,被误诊为包虫囊肿。 FDG PET / CT被要求对该肿块进行代谢表征,并显示该病灶的固体成分轻度至中度过度代谢。进行手术切除并组织学检查发现神经鞘瘤。简介Schwannoma是一种良性肿瘤,起源于周围神经和颅神经周围的Schwann细胞。它易患上,下肢的头颈部和下肢表面(1)。Schwannoma最常见于20至50岁的患者,男性多于女性(2)。它们占所有良性软组织肿瘤的5%(3)。胸壁和diaphragm肌神经鞘瘤很少见。神经鞘瘤通常偶然发现或出现模糊,非特定症状。这种良性肿瘤几乎总是生长缓慢,非侵袭性肿瘤,并且在大多数情况下是单发的。 5%至18%的神经鞘瘤与I型神经纤维瘤病相关(4),在这种情况下,病变可能是多发的,通常是丛状的。恶性转化非常罕见。从外观上看,神经鞘瘤通常被视为孤立的,界限分明的,包囊的病变(5)。明确的诊断仍是组织学上的。从组织学上讲,典型的神经鞘瘤由混合的安东尼A成分(细胞和短束或交错束排列)和安东尼B区域(较少的细胞和更多的类胶质成分组成)组成。细胞变体(包括大多数大型腹膜后和盆腔神经鞘瘤)具有均匀的梭形细胞外观,无安东尼A区或B区。特征在于,所有神经鞘瘤均显示S100蛋白均匀且强烈的染色(6)。对于放射科医生来说,考虑到腹膜后或盆腔肿块,考虑良性神经鞘瘤的诊断很重要,以避免不必要的手术,因为这些病变可以保守处理(3)。在本病例报告中,我们旨在报告由右隔膜引起的异常定位的神经鞘瘤的FDG PET / CT结果。病例报告一名患有咳嗽和痰的39岁男子被转诊至胸科门诊。进行了诊断计算机断层扫描(CT)。它显示出来自右diaphragm肌的包囊,轮廓分明,圆形,异质囊性软组织肿块。测量病变的直径约10厘米,并从right肌的右穹顶一直延伸到右肾的上极。由于土耳其是棘球E虫感染的地方性国家,因此根据其CT模式,它最初被误诊为包虫囊肿。 F-18脱氧葡萄糖(FDG)PET / CT被要求排除可能的恶性肿瘤。 (A)轴向,(B)冠状,(C)矢状PET,CT和PET / CT组合图像显示,位于以下部位的固体成分的FDG摄取量轻至中度[最大标准摄取值(SUVmax):4,1]。行全切除术,组织学检查发现为良性神经鞘瘤。

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