Isolated Juvenile Xanthogranuloma in Thoracic Spine: Intraoperative Cytological Diagnosis of a Rare Presentation

Shashi Singhvi, S. Bhargava
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Abstract

Juvenile Xanthogranulomas (JXG) are benign proliferative disorders of non-Langerhans histiocytes, which present in children as multiple, self-limited, cutaneous lesions. The extracutaneous manifestations of JXG are uncommon, and isolated JXG involving the spinal column is extremely rare. We report here a case of isolated juvenile xanthogranuloma in thoracic spine correctly diagnosed intraoperatively on crush smear cytology and later confirmed by histopathological and immunohistochemical studies. This case report draws attention to the fact that isolated xanthogranuloma should be considered among possible diagnoses of spinal tumor in children. Also, since the long term survival depends on complete surgical resection, a correct intraoperative diagnosis is extremely important for optimal management and prognosis of the patient.
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胸椎孤立幼年黄色肉芽肿:术中细胞学诊断的罕见表现
幼年型黄色肉芽肿(JXG)是一种非朗格汉斯组织细胞的良性增殖性疾病,在儿童中表现为多发性、自限性皮肤病变。JXG的皮外表现并不常见,而累及脊柱的孤立性JXG极为罕见。我们在此报告一例胸椎孤立的幼年黄色肉芽肿,术中经碾压涂片细胞学正确诊断,后经组织病理学和免疫组织化学研究证实。本病例报告提请注意,孤立的黄色肉芽肿应考虑在可能的诊断脊柱肿瘤的儿童。此外,由于长期生存依赖于完全的手术切除,正确的术中诊断对于患者的最佳管理和预后至关重要。
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