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Letson, G. Douglas

https://orcid.org/0000-0001-5344-4316

Mayo Clinic

Moffitt Cancer Center

Citations 3

A Modified Lodwick-Madewell Grading System for the Evaluation of Lytic Bone Lesions
Caracciolo, Jamie T., Temple, H. Thomas , Letson, G. Douglas , Kransdorf, Mark J.

American Journal of Roentgenology | April 12, 2016 | Volume: 207 | Issue: 1 | Pages: 150-156

10.2214/ajr.15.14368 Get It

Primary Bone Tumors: Epidemiologic Comparison of 9200 Patients Treated at Beijing Ji Shui Tan Hospital, Beijing, China, With 10 165 Patients at Mayo Clinic, Rochester, Minnesota
Niu, Xiaohui , Xu, Hairong , Inwards, Carrie Y., Letson, G. Douglas , Bui, Marilyn M, Li, Yuan, Ding, Yi , Bui, Marilyn M.

Archives of Pathology & Laboratory Medicine | May 15, 2015 | Volume: 139 | Issue: 9 | Pages: 1149-1155

10.5858/arpa.2014-0432-oa Get It

Context Although primary bone tumors are extremely rare, the literature suggests that there are variations in the epidemiologic characteristics in different populations. The most frequently cited epidemiologic characteristics of primary bone tumors are derived from a large US series (Mayo Clinic), with no comparable study thus far performed in China. Objective To identify any potential epidemiologic differences between Chinese patients and a US series of patients. Design We performed a comparison study between 9200 patients treated at Beijing Ji Shui Tan Hospital (JST) and 10 165 patients treated at Mayo Clinic (MC), Rochester Minnesota. Detailed epidemiologic features were analyzed. Results We found that giant cell tumor and osteosarcoma have significantly higher incidences in the JST than the MC patients (P < .001). However, JST patients had a significantly lower incidence of Ewing sarcoma, chordoma, fibrosarcoma, myeloma, and malignant lymphoma (P < .001). For most benign and malignant bone tumors, the Chinese cohort had a more distinct male predominance than the US cohort. Malignant bone tumors had a monomodal age distribution in the JST patient group, with a bimodal age distribution in the MC cohort. Also, there were was a predilection for tumors of the femur and tibia among the JST patients (P < .001). Conclusions Our data confirm that epidemiologic variations of primary bone tumors exist in different populations. Factors that may contribute to these observed differences are proposed and discussed.
Classification of failure of limb salvage after reconstructive surgery for bone tumours
Ruggieri, Pietro , Windhager, Reinhard , Funovics, Philipp T. , Gibbons, C. L. M. H. , Hornicek, Francis J. , Temple, H. Thomas , Letson, G. Douglas , Henderson, Eric R. , O’Connor, Mary I. , Guo, Wei , Ruggieri, Pietro

The Bone & Joint Journal | November 4, 2014 | Volume: 96-B | Issue: 11 | Pages: 1436-1440

10.1302/0301-620x.96b11.34747 Get It

Previous classification systems of failure of limb salvage focused primarily on endoprosthetic failures and lacked sufficient depth for the effective study of the causes of failure. In order to address these inadequacies, the International Society of Limb Salvage (ISOLS) formed a committee to recommend revisions of the previous systems. The purpose of this study was to report on their recommendations. The modifications were prepared using an earlier, evidence-based model with subclassification based on the existing medical literature. Subclassification for all five primary types of failure of limb salvage following endoprosthetic reconstruction were formulated and a complementary system was derived for the failure of biological reconstruction. An additional classification of failure in paediatric patients was also described. Limb salvage surgery presents a complex array of potential mechanisms of failure, and a complete and precise classification of types of failure is required. Earlier classification systems lacked specificity, and the evidence-based system outlined here is designed to correct these weaknesses and to provide a means of reporting failures of limb salvage in order to allow the interpretation of outcome following reconstructive surgery. Cite this article: Bone Joint J 2014;96-B:1436–40.