Wren Ethan, Goodwin Tyler M, Brazier Brett G, Marinas Edwin, Katranji Abdalmajid
Department of Orthopaedic Surgery, Michigan State University, East Lansing, MI 48824, USA.
Department of Orthopaedic Surgery, University of Tennessee College of Medicine Chattanooga, Chattanooga, TN 37403, USA.
J Orthop Case Rep. 2020 Nov;10(8):84-87. doi: 10.13107/jocr.2020.v10.i08.1872.
The following report describes a rare case of giant cell tumor (GCT) of the bone that presented in the distal phalanx of the thumb. GCT of the bone is a relatively rare, and typically benign condition that presents most frequently in the metaphysis of long bones in women age 30-50 years old. There are only three other instances in the literature describing GCT of the bone presenting in the distal phalanx of the thumb. Although rare, delayed or missed diagnosis can be very debilitating to the patient.
A 28-year-old male laborer who is right hand dominant and works with his hands for a living presented to the emergency department (ED) with swelling and pain at the distal aspect of his left thumb with no known injury. The patient was seen 4 weeks previously and was treated for cellulitis of the hand with antibiotics. At that time, no radiographs were taken. Despite this treatment, the patient reported increased swelling and pain over the next 2 weeks. He then sought treatment in the ED where a hand surgeon was consulted and radiographs were obtained that displayed a lytic, disruptive, and mildly expansile lesion of the distal phalanx of the first finger concerning for sarcoma. The risks and benefits of surgery were discussed with the patient and surgical intervention was planned.
Due to how rarely this condition presents clinically, the patient was initially misdiagnosed and definitive treatment was delayed. Although rare, this is an important diagnosis to consider in patients presenting similarly. The patient ultimately received adequate treatment, but the delay in diagnosis in combination with the locally aggressive nature of this tumor could have led to extensive surgical intervention with impairment in hand function. As a laborer whose income relies on daily use of his hands a delayed diagnosis; in this case could have had a catastrophic impact.
以下报告描述了一例罕见的骨巨细胞瘤(GCT),该肿瘤发生于拇指远节指骨。骨巨细胞瘤是一种相对罕见的疾病,通常为良性,最常见于30至50岁女性长骨的干骺端。文献中仅有另外三例描述骨巨细胞瘤发生于拇指远节指骨的病例。尽管罕见,但延迟诊断或漏诊可能会给患者带来极大的痛苦。
一名28岁的男性体力劳动者,惯用右手,以手工劳动为生,因左手拇指远端肿胀疼痛就诊于急诊科(ED),无已知外伤史。该患者4周前曾就诊,因手部蜂窝织炎接受抗生素治疗。当时未进行X线检查。尽管接受了治疗,但患者报告在接下来的2周内肿胀和疼痛加剧。随后他到急诊科寻求治疗,咨询了手外科医生并进行了X线检查,结果显示示指远节指骨有一个溶骨性、破坏性且轻度膨胀性的病变,怀疑为肉瘤。与患者讨论了手术的风险和益处,并计划进行手术干预。
由于这种疾病在临床上极为罕见,患者最初被误诊,明确治疗被延迟。尽管罕见,但对于表现相似的患者,这是一个需要考虑的重要诊断。患者最终接受了充分的治疗,但诊断延迟加上该肿瘤的局部侵袭性可能导致广泛的手术干预并影响手部功能。作为一名收入依赖于日常手部使用的体力劳动者,诊断延迟在这种情况下可能会产生灾难性的影响。