Natural history of multiple hereditary osteochondromatosis of the lower extremity and ankle

被引:39
|
作者
Noonan, KJ [1 ]
Feinberg, JR [1 ]
Levenda, A [1 ]
Snead, J [1 ]
Wurtz, LD [1 ]
机构
[1] Indiana Univ, Sch Med, Indianapolis, IN USA
关键词
ankle osteoarthritis; multiple hereditary osteochondromatosis;
D O I
10.1097/00004694-200201000-00025
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
In this study the authors evaluated the natural history of the ankle joint in patients with multiple hereditary osteochondromatosis. Thirty-eight subjects With an average age of 42 years completed a detailed subjective questionnaire and underwent clinical and radiographic evaluation of their ankles. Three subjects (8%) indicated their ankle involvement affected their vocation, and 12 (32%) Were limited in recreational sports. Seven patients (18%) had pain in at least one ankle on a weekly basis, with an average ankle pain score of 2.2. Ankle range of motion averaged 50 degrees and subtalar motion was considered normal in two thirds of ankles. Radiographic evaluation documented an average tibiotalar tilt of 9 degrees of ankle valgus, with evidence of degenerative joint disease noted in 14 ankles (19%). Those with arthritic changes had significantly more tibiotalar tilt and diminished ankle range of motion compared with those without radiographic signs of osteoarthritis. These findings document measurable decreases in ankle function and suggest that correction or prevention of excessive tibiotalar tilt may be warranted to improve outcome.
引用
收藏
页码:120 / 124
页数:5
相关论文
共 50 条
  • [1] Multiple hereditary osteochondromatosis - Two cases with ankle and knee deformities
    Glockenberg, A
    Sobel, E
    Levitz, SJ
    [J]. JOURNAL OF THE AMERICAN PODIATRIC MEDICAL ASSOCIATION, 1997, 87 (02): : 70 - 73
  • [2] Multiple hereditary osteochondromatosis in a family
    Santos-Guzman, Jesus
    Cantu-Reyna, Consuelo
    Cano-Munoz, Ignacio
    Karen Pulido-Ayala, Ana
    Garcia, Adrian
    [J]. BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO, 2016, 73 (02): : 111 - 116
  • [3] A Case of Multiple Hereditary Osteochondromatosis
    Sepulveda-Acosta, Julio N.
    Gomez-Cintron, Angel
    [J]. PUERTO RICO HEALTH SCIENCES JOURNAL, 2011, 30 (04) : 212 - 212
  • [4] The Natural History of Lower Extremity Malalignment
    McClure, Philip K.
    Herzenberg, John E.
    [J]. JOURNAL OF PEDIATRIC ORTHOPAEDICS, 2019, 39 (06) : S14 - S19
  • [5] Management of forearm deformity in multiple hereditary osteochondromatosis
    Arms, DM
    Strecker, WB
    Manske, PR
    Schoenecker, PL
    [J]. JOURNAL OF PEDIATRIC ORTHOPAEDICS, 1997, 17 (04) : 450 - 454
  • [6] Hereditary multiple osteochondromatosis: a familial case of an unusual pathology
    Maduro, Ana Isabel
    Saraiva, Andre Pinto
    Malcata, Armando
    Coutinho, Margarida
    [J]. RHEUMATOLOGY, 2021, 60 (12) : 5879 - 5879
  • [7] WAVY PELVIS SIGN IN CT OF MULTIPLE HEREDITARY OSTEOCHONDROMATOSIS
    PORTER, G
    ALLARD, J
    [J]. JOURNAL OF COMPUTER ASSISTED TOMOGRAPHY, 1992, 16 (01) : 126 - 128
  • [8] THE NATURAL-HISTORY OF HEREDITARY MULTIPLE EXOSTOSES
    SCHMALE, GA
    CONRAD, EU
    RASKIND, WH
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1994, 76A (07): : 986 - 992
  • [9] Lower extremity scintigraphy: The foot and ankle
    Groshar, D
    Gorenberg, M
    Ben-Haim, S
    Jerusalmi, J
    Liberson, A
    [J]. SEMINARS IN NUCLEAR MEDICINE, 1998, 28 (01) : 62 - 77
  • [10] Multiple hereditary osteochondromatosis with spinal cord compression: case report
    Garcia-Gonzalez, Oscar
    Nicolas Mireles-Cano, J.
    Sanchez-Zavala, Natalia
    Chagolla-Santillan, Miguel A.
    Orozco-Ramirez, Segio M.
    Silva-Cerecedo, Pedro
    Murguia-Perez, Mario
    Rueda-Franco, Fernando
    [J]. CHILDS NERVOUS SYSTEM, 2018, 34 (03) : 565 - 569