A Rare Case of Isolated Central Nervous System Neoplasm With Histiocytic Features.

Yoonsoo Choi, Yujin Lee, Young Il Kim, Seung Ho Yang
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Abstract

This paper discusses a rare case of a 49-year-old female diagnosed with a central nervous system-isolated neoplasm with histiocytic features, classified as histiocytic neoplasm, not otherwise specified (NOS). Despite comprehensive histopathological and genetic studies, accurately diagnosing the case proved challenging. Initial surgical findings and frozen biopsy suggested a low-grade glioma; however, subsequent immunohistochemistry and genetic analysis excluded known histiocytic subtypes such as ALK-positive histiocytosis and Erdheim-Chester disease. The patient's condition improved following occupational rehabilitation therapy for right upper motor weakness, as well as anticonvulsant and radiation therapy, and her neurological condition remains stable. This case underscores the diagnostic challenges of Histiocytic Neoplasms and the necessity for interdisciplinary collaboration and sophisticated diagnostic techniques.

具有组织细胞特征的孤立中枢神经系统肿瘤1例。
本文讨论了一例罕见的49岁女性诊断为具有组织细胞特征的中枢神经系统分离性肿瘤,归类为组织细胞性肿瘤,未另行说明(NOS)。尽管进行了全面的组织病理学和遗传学研究,但准确诊断该病例仍具有挑战性。最初的手术结果和冷冻活检提示为低级别胶质瘤;然而,随后的免疫组织化学和遗传分析排除了已知的组织细胞亚型,如alk阳性组织细胞增多症和Erdheim-Chester病。患者接受右上运动无力的职业康复治疗、抗惊厥药和放射治疗后病情好转,神经系统状况稳定。这个病例强调了组织细胞肿瘤的诊断挑战,以及跨学科合作和复杂诊断技术的必要性。
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