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Intra-articular acetabular osteochondroma in patients with multiple hereditary exostoses.
Choudhry, Ashima; Gimm, Geunwu; Kang, Ho Won; Shin, Chang Ho; Yoo, Won Joon; Choi, In-Ho; Cho, Tae-Joon.
Affiliation
  • Choudhry A; Division of Pediatric Orthopaedics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
  • Gimm G; Department of Orthopaedic Surgery, ASUTOSH Hospital, Surat, Gujarat, India.
  • Kang HW; Division of Pediatric Orthopaedics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
  • Shin CH; Division of Pediatric Orthopaedics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
  • Yoo WJ; Division of Pediatric Orthopaedics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
  • Choi IH; Department of Orthopaedic Surgery, Seoul National University College of Medicine, Seoul, Republic of Korea.
  • Cho TJ; Division of Pediatric Orthopaedics, Seoul National University Children's Hospital, Seoul, Republic of Korea.
J Pediatr Orthop B ; 31(1): e90-e94, 2022 Jan 01.
Article in En | MEDLINE | ID: mdl-34848667
ABSTRACT
We report three additional cases of intra-articular acetabular osteochondroma in multiple hereditary exostoses patients in order to raise the awareness of this rare location, to prompt early diagnosis, and to present various treatment options according to the patient's condition. A 2.5-year-old boy presenting with an out-toeing gait had a large acetabular osteochondroma causing lateral displacement of the femoral head and acetabular dysplasia. Mass excision through hip subluxation via anterior approach and concomitant Dega osteotomy resulted in a congruent, well-developed, and well-covered hip joint at 11-year follow-up. A 10-year-old boy showing a pedunculated osteochondroma arising from the triradiate cartilage was successfully treated by arthroscopic excision. Normal development of the hip joint was observed at skeletal maturity. A 6-year-old boy presented with a painless limp. Acetabular osteochondroma could be confirmed by computed tomography scan, which was excised through hip subluxation by anterior approach. Persistent coxa valga and femoral head uncovering were addressed by femoral varization osteotomy at 9 years of age. A high index of suspicion is required to detect a lesion at this rare location. Various procedures may be considered according to the pathoanatomy. Acetabular dysplasia, coxa valga, and femoroacetabular impingement by femur neck mass, if associated, should be addressed in due time.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteochondroma / Exostoses, Multiple Hereditary / Hip Dislocation Type of study: Screening_studies Limits: Child / Child, preschool / Humans / Male Language: En Journal: J Pediatr Orthop B Journal subject: ORTOPEDIA / PEDIATRIA Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone Neoplasms / Osteochondroma / Exostoses, Multiple Hereditary / Hip Dislocation Type of study: Screening_studies Limits: Child / Child, preschool / Humans / Male Language: En Journal: J Pediatr Orthop B Journal subject: ORTOPEDIA / PEDIATRIA Year: 2022 Document type: Article
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