Atypical Skull Base Metastasis from Pediatric Extremity Chondroblastic Osteosarcoma Detected by Surveillance 18F-FDG PET/CT: A Case Report with Focused Literature Review.

IF 0.9 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Seçkin Bilgiç, Hüseyin Galip Şahin, İrem Köroğlu, Ulviye Yalçınkaya, Eray Alper
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引用次数: 0

Abstract

A 15-year-old girl who had previously undergone surgery and chemotherapy for non-metastatic chondroblastic osteosarcoma of the left fibula was evaluated with 18F-fluorodeoxyglucose positron emission tomography/computed tomography (18F-FDG PET/CT) during routine follow-up while in clinical remission. Imaging demonstrated a 36 × 17 mm hypermetabolic lesion in the right occipital condyle maximum standard uptake value [(SUVmax): 16.5], with adjacent bone and soft-tissue extension, together with a concurrent 18F-FDG-avid pulmonary nodule (SUVmax: 3.4). Shortly after imaging, the patient developed mild neck discomfort and right-sided tongue deviation, suggesting hypoglossal nerve involvement. Biopsy of the skull base lesion and histopathological evaluation of the pulmonary nodule confirmed metastatic chondroblastic osteosarcoma with concordant morphology and immunophenotype. The patient underwent biopsy of the occipital lesion, surgical excision, radiotherapy, and wedge resection of the pulmonary metastasis. Skull base involvement from osteosarcoma arising in the extremities is exceptional and is particularly rare in pediatric patients. This case highlights the complementary role of whole-body 18F-FDG PET/CT in detecting atypical metastatic sites that may not be routinely assessed by conventional surveillance strategies. In addition, the focused literature review underscores the exceptional rarity of skull base involvement in pediatric chondroblastic osteosarcoma and supports the need for heightened awareness of uncommon metastatic patterns.

监测18F-FDG PET/CT检测儿童四肢软骨母细胞骨肉瘤不典型颅底转移一例报告并重点文献复习。
一名15岁的女孩曾因左腓骨非转移性软骨成骨肉瘤接受手术和化疗,在临床缓解期间,在常规随访期间使用18f -氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(18F-FDG PET/CT)进行评估。影像学显示右侧枕髁有一个36 × 17 mm的高代谢病变,最大标准摄取值[(SUVmax): 16.5],伴有邻近的骨和软组织延伸,并发18F-FDG-avid肺结节(SUVmax: 3.4)。成像后不久,患者出现轻度颈部不适和右侧舌偏,提示舌下神经受累。颅底病变活检和肺结节的组织病理学评估证实转移性软骨母细胞骨肉瘤具有一致的形态和免疫表型。患者接受了枕部病变活检、手术切除、放疗和肺转移灶楔形切除。四肢骨肉瘤累及颅底是罕见的,在儿科患者中尤其罕见。该病例强调了全身18F-FDG PET/CT在检测非典型转移部位方面的补充作用,这些部位可能无法通过常规监测策略进行常规评估。此外,重点文献综述强调了儿童成软骨骨肉瘤中颅底病变的罕见性,并支持提高对罕见转移模式的认识。
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来源期刊
Molecular Imaging and Radionuclide Therapy
Molecular Imaging and Radionuclide Therapy RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
CiteScore
1.30
自引率
0.00%
发文量
50
期刊介绍: Molecular Imaging and Radionuclide Therapy (Mol Imaging Radionucl Ther, MIRT) is publishes original research articles, invited reviews, editorials, short communications, letters, consensus statements, guidelines and case reports with a literature review on the topic, in the field of molecular imaging, multimodality imaging, nuclear medicine, radionuclide therapy, radiopharmacy, medical physics, dosimetry and radiobiology.
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