Beatson West of Scotland Cancer Centre, Glasgow Royal Infirmary, Glasgow, Scotland.
Departments of General Surgery, Glasgow Royal Infirmary, Glasgow, Scotland.
J Med Case Rep. 2023 Oct 6;17(1):419. doi: 10.1186/s13256-023-04156-w.
This case reports the synchronous diagnosis of two rare unrelated diseases; leiomyosarcoma and tenosynovial giant cell tumor of the knee. It focuses on the challenges of diagnosing tenosynovial giant cell tumor, including cognitive biases in clinical medicine that delay diagnosis. It also demonstrates the pathogenic etiology of tenosynovial giant cell tumor, evidenced by the transient deterioration of the patients' knee symptoms following the administration of prophylactic granulocyte colony-stimulating factor given as part of the chemotherapeutic regime for leiomyosarcoma.
A 37-year-old Caucasian man presented with a left groin lump and left knee pain with swelling and locking. Investigations including positron emission tomography-computed tomography and biopsy revealed leiomyosarcoma in a lymph node likely related to the spermatic cord, with high-grade uptake in the left knee that was presumed to be the primary site. His knee symptoms temporarily worsened each time granulocyte colony-stimulating factor was administered with each cycle of chemotherapy for leiomyosarcoma to help combat myelosuppressive toxicity. Subsequent magnetic resonance imaging and biopsy of the knee confirmed a tenosynovial giant cell tumor. His knee symptoms relating to the tenosynovial giant cell tumor improved following the completion of his leiomyosarcoma treatment.
Tenosynovial giant cell tumor remains a diagnostic challenge. We discuss the key clinical features and investigations that aid prompt diagnosis. The National Comprehensive Cancer Network clinical practice guidelines for soft tissue sarcoma have recently been updated to include the pharmacological management of tenosynovial giant cell tumor. Our case discussion provides an up-to-date review of the evidence for optimal management of patients with tenosynovial giant cell tumor, with a particular focus on novel pharmacological options that exploit underlying pathogenesis.
本病例报告同时诊断出两种罕见的不相关疾病;平滑肌肉瘤和膝关节腱鞘巨细胞瘤。重点介绍了诊断腱鞘巨细胞瘤的挑战,包括临床医学中的认知偏差会导致诊断延迟。还展示了腱鞘巨细胞瘤的发病机制病因,患者膝关节症状在接受预防性粒细胞集落刺激因子治疗后暂时恶化,这是作为平滑肌肉瘤化疗方案的一部分。
一名 37 岁白人男性,因左腹股沟肿块和左膝疼痛伴肿胀和交锁就诊。包括正电子发射断层扫描-计算机断层扫描和活检的检查结果显示,可能与精索相关的淋巴结中存在平滑肌肉瘤,左膝有高级别摄取,推测为原发性部位。每次接受化疗治疗平滑肌肉瘤时,每次给予粒细胞集落刺激因子都会导致他的膝关节症状暂时恶化,以帮助对抗骨髓抑制毒性。随后的膝关节磁共振成像和活检证实为腱鞘巨细胞瘤。完成平滑肌肉瘤治疗后,他的膝关节与腱鞘巨细胞瘤相关的症状有所改善。
腱鞘巨细胞瘤仍然是一个诊断挑战。我们讨论了有助于快速诊断的关键临床特征和检查。国家综合癌症网络软组织肉瘤临床实践指南最近已更新,包括腱鞘巨细胞瘤的药物治疗管理。我们的病例讨论提供了腱鞘巨细胞瘤患者最佳管理的最新证据综述,特别关注利用潜在发病机制的新型药物选择。