Rationale: Osteoid osteoma, accounting for approximately 10% of benign bone tumors, is predominantly found in long bones and rarely in the foot bones, such as the talus. Its nonspecific symptoms, such as nocturnal pain and swelling, often lead to misdiagnosis, especially when it mimics conditions like ankle synovitis.
Patient Concerns: A 27-year-old male presented with persistent pain and swelling in his left ankle following an injury at the gym. Initial treatments, including arthroscopic debridement, failed to resolve his symptoms.
Diagnoses: Comprehensive evaluation using magnetic resonance imaging and computed tomography scans, coupled with input from a multidisciplinary team of specialists, confirmed the diagnosis of ankle osteoid osteoma.
Interventions: Following the confirmation of the diagnosis, the patient underwent surgical interventions, including peripheral nerve transfer, joint debridement, resection of calcaneal and talus lesions, and tendon release. These procedures were designed to address the underlying tumor and restore joint function.
Outcomes: After surgical intervention, the patient experienced substantial relief from pain and significant improvement in functional recovery. Postoperative rehabilitation further facilitated the restoration of mobility and strength, with no recurrence of symptoms observed during follow-up.
Lessons: This case highlights the diagnostic complexity of ankle osteoid osteoma and underscores the importance of a multidisciplinary approach. Rehabilitation therapists play a crucial role in managing such conditions, ensuring optimal patient outcomes through functional assessment and progress monitoring. Timely and accurate diagnosis is essential for effective treatment and improved patient quality of life.
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http://dx.doi.org/10.1097/MD.0000000000040682 | DOI Listing |
Int J Surg Pathol
January 2025
Department of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Osteoid osteoma is a benign bone tumor commonly affecting young individuals, with a rare occurrence in older adults. It typically presents with night pain relieved by nonsteroidal anti-inflammatory drugs and is characterized radiographically by a small, radiolucent nidus surrounded by reactive sclerosis. We present a 70-year-old female patient with persistent right hip pain, initially diagnosed as arthritis, who underwent total hip arthroplasty.
View Article and Find Full Text PDFInt J Surg Case Rep
January 2025
Bone and Joint Diseases Research Center, Department of Orthopedic Surgery, Shiraz University of Medical Sciences, Iran; Golestan Rhematology Research Center, Golestan University of Medical Sciences, Gorgan, Iran. Electronic address:
Introduction And Importance: Osteoid osteoma (OO) is a common benign bone tumor, mostly affecting young adults. Since it often develops in long bones, OO is rarely considered as a cause of chronic shoulder pain.
Case Presentation: We treated an 8-year-old boy with ongoing shoulder pain that was worse at night but improved with NSAIDs.
Eur J Radiol
December 2024
Department of Radiology, University Hospital, LMU Munich, Marchioninistr. 15, D-81377 Munich, Germany.
Objectives: To evaluate the influence of clinical and procedural factors, particularly the thickness of reactive sclerosis, on clinical outcome of MR-guided high-intensity focused ultrasound (MR-HIFU) for the treatment of symptomatic osteoid osteomas (OO) of the extremities.
Materials And Methods: 18 consecutive patients (median age 19.5y) with symptomatic OO of the extremities eligible for MR-HIFU were enrolled in this ongoing prospective study (German Clinical Trials Register; nr.
Radiol Case Rep
February 2025
Loyola University Medical Center and Loyola University Chicago, 2160 S First Ave, Maywood, IL 60153, USA.
Osteoid osteoma (OO), a benign bone-forming tumor estimated to account for 3% of all primary bone tumors, rarely occurs in the finger. This case report presents an unusual instance of osteoid osteoma in the finger of a 15-year-old male patient. The lesion was discovered following an initial patient visit for left middle finger pain and swelling for one year without any identifiable injuries.
View Article and Find Full Text PDFChilds Nerv Syst
December 2024
Departement of Pediatric Neurosurgery, Hôpital Femme Mère Enfant, Lyon, France.
Background And Aim: Osteoid osteoma (Oo) and osteoblastoma (Ob) are rare primary bone tumors with a higher prevalence in the second decade of life. Treatment can be conservative, but in cases of spinal location, resective surgery is of great importance but may be challenging.
Material And Methods: We report four pediatric cases of Oo and Ob managed in our unit, with different locations at the level of the cervical spine.
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