García-Jiménez Antonio, Chanes-Puiggrós Camila, Trullols-Tarragó Laura, Pulido-García María-Carmen
* Department of Orthopedic Surgery, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
† Division of Orthopedic Oncology, Department of Orthopedic Surgery, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
J Hand Surg Asian Pac Vol. 2019 Mar;24(1):45-49. doi: 10.1142/S2424835519500085.
Primary malignant tumours of the hand are extremely rare, with chondrosarcoma being the most common. We describe six consecutive cases of chondrosarcoma (CS) of the hand, with a follow-up of 12 months to 10 years after surgical intervention.
Five cases were primary tumors and one was secondary to Ollier's disease. Mean age at diagnosis was 67.5 years (range 46 to 85 years) and three patients were males. The bone most commonly affected was the proximal phalanx (in 4 patients), followed by the metacarpal bone (3 cases in the other 2 patients). The first symptom was an increase in volume in five cases and a pathological fracture in one. The x-ray study showed signs of malignancy in two cases only. In the other four cases, CT and MRI studies were necessary to complete the diagnosis.
Primary amputation was performed in two cases and intralesional curettage and cancellous bone autograft in four. Primary amputation was performed in two cases and intralesional curettage and cancellous bone autograft in four. We found three grade I/III CS and three grade II/III CS in the histological study. Local recurrences occurred in three patients, two being grade II/III CS. One of the three had undergone an initial amputation and underwent re-amputation, another had had curettage of the lesion and was amputated, and the third patient decided not to undergo the procedure due to her age. A pulmonary nodule was suspected at the most recent follow up in a fourth patient, who had been diagnosed with a grade II/III CS.
Although CS of the hand bones behaves as a locally aggressive lesion, it rarely metastasizes. Intralesional curettage with a cancellous bone autograft appears to be a good option in low-grade CS to preserve the function, keeping in mind the high rate of recurrence. Wide excision or amputation is recommended when severe joint deformity or soft tissue involvement interferes with hand function.
手部原发性恶性肿瘤极为罕见,其中软骨肉瘤最为常见。我们描述了连续6例手部软骨肉瘤(CS)病例,术后随访12个月至10年。
5例为原发性肿瘤,1例继发于骨软骨瘤病。诊断时的平均年龄为67.5岁(范围46至85岁),3例为男性。最常受累的骨骼是近节指骨(4例患者),其次是掌骨(另外2例患者中的3例)。首发症状5例为体积增大,1例为病理性骨折。X线检查仅2例显示恶性征象。其他4例需要CT和MRI检查以完成诊断。
2例行一期截肢术,4例行病灶内刮除加松质骨自体骨移植术。组织学研究发现3例I/III级CS和3例II/III级CS。3例患者出现局部复发,其中2例为II/III级CS。3例中的1例最初接受了截肢术,后来再次截肢;另1例对病灶进行了刮除术,随后截肢;第3例患者因年龄原因决定不接受手术。第4例诊断为II/III级CS的患者在最近一次随访时疑似出现肺结节。
尽管手部骨骼的CS表现为局部侵袭性病变,但很少发生转移。对于低级别CS,病灶内刮除加松质骨自体骨移植似乎是保留功能的良好选择,但要注意复发率较高。当严重的关节畸形或软组织受累影响手部功能时,建议广泛切除或截肢。