Adamantinomatous tumors: Long-term follow-up study of 20 patients treated at a single institution

被引:6
|
作者
Schwarzkopf, Eugenia [1 ]
Tavarez, Yoely [2 ]
Healey, John H. [2 ]
Hameed, Meera [3 ]
Prince, Daniel E. [2 ]
机构
[1] Sloan Kettering Inst, New York, NY USA
[2] Mem Sloan Kettering Canc Ctr, Dept Surg, Orthopaed Serv, 1275 York Ave, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
adamantinoma; bone-tumor; low-grade; osteofibrous dysplasia; OSTEOFIBROUS DYSPLASIA; BONES; TIBIA; DIFFERENTIATION;
D O I
10.1002/jso.25950
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and Objectives Adamantinomas are primary, low-grade malignant tumors of the bone that have metastatic potential to the lungs, lymph nodes, and other regions. The rarity of this disease and its nonspecific symptoms complicate diagnosis. Materials and Methods Records for 20 patients who underwent treatment for adamantinoma from 1975 to 2018 were reviewed for demographic, clinical, and pathological data, treatment details, postoperative complications, and outcomes. Results Patients presented at a median age of 22 years (1-79 years): 14 patients had a localized primary tumor, three presented with local recurrence, and three with metastatic disease. Median tumor size was 5.7 cm (0.5-15.5 cm). Wide excision was performed primarily in 15 cases; the remaining five patients underwent intralesional curettage. At a median follow-up of 7.3 years, 14 patients had no evidence of disease; two patients were alive with disease, and four patients died from the disease. Local recurrence and distant metastasis occurred at a median of 11.4 years (6 month-19 years) and 15.8 years (4 month-23 years) after diagnosis. Conclusions Adequate histopathological diagnosis is crucial to avoid misdiagnosis of this rare tumor. Local and distant recuAbs_Para_meprrence can occur more than 20 years after the initial diagnosis. Life-long follow-up with clinical examination and imaging is required.
引用
收藏
页码:273 / 282
页数:10
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