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Abstract：
This study investigated the infrequent occurrence of tonsillar follicular dendritic cell sarcoma (FDCS) co-existing with schizophrenia, presenting a comprehensive examination of clinical, pathological, and literature aspects. A systematic literature review was conducted, focusing on articles related to \"schizophrenia\" and \"sarcoma,\" with in-depth analysis of included case reports. Clinical data, pathological findings, and patient follow-up information were collected and synthesized. The study detailed a rare case of FDCS in the tonsil concurrent with schizophrenia, providing insights into diagnosis, treatment, and follow-up. A literature review of combined FDCS in the tonsil and schizophrenia cases highlighted their clinical and pathological characteristics. Eight case reports encompassing 11 patients diagnosed with sarcoma and schizophrenia were included. Surgical resection was the preferred primary treatment, while chemotherapy was suggested for recurrences. Instances of co-occurring FDCS and schizophrenia were exceptionally limited, with tonsillar FDCS being particularly uncommon. The coexistence of tonsillar FDCS and schizophrenia was an exceptionally rare condition, posing diagnostic and therapeutic challenges. This study contributed valuable insights into clinical and pathological practice through a systematic review, underscoring the significance of early diagnosis and comprehensive management.
摘要：
这项研究调查了与精神分裂症并存的扁桃体滤泡树突状细胞肉瘤（FDCS）的罕见发生，提供全面的临床检查，病态,和文学方面。进行了系统的文献综述，关注与“精神分裂症”和“肉瘤”相关的文章，“对纳入的病例报告进行深入分析。临床数据,病理结果，收集和合成患者随访信息。该研究详述了扁桃体中并发精神分裂症的罕见FDCS病例，提供对诊断的见解，治疗,和后续行动。扁桃体和精神分裂症患者合并FDCS的文献综述强调了其临床和病理特征。包括8例病例报告，包括11例诊断为肉瘤和精神分裂症的患者。手术切除是首选的主要治疗方法，而化疗建议复发。同时发生的FDCS和精神分裂症的例子非常有限，扁桃体FDCS特别罕见。扁桃体FDCS和精神分裂症共存是一种非常罕见的疾病，构成诊断和治疗挑战。这项研究通过系统评价为临床和病理实践提供了有价值的见解，强调早期诊断和综合管理的重要性。
