{"title":"Presentation of osteoid osteoma in the fifth metatarsal: a case report and review of the literature.","authors":"Ehsan Behzadi, Mohammadhadi Mollaabbasi","doi":"10.1186/s13256-025-05366-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Osteoid osteoma is a benign bone tumor commonly affecting the lower extremities, typically the femur or tibia. However, its occurrence in the fifth metatarsal bone is rare, and atypical presentations can lead to delayed diagnosis and misinterpretation as other pathologies.</p><p><strong>Case presentation: </strong>We report the case of a 14-year-old Persian male athlete who presented with persistent lateral forefoot pain lasting 2 years, initially attributed to a traumatic injury. The pain was progressively worsening, nocturnal, and unresponsive to nonsteroidal anti-inflammatory drugs, deviating from the classical dramatic relief associated with this tumor. Radiographs initially showed diffuse sclerosis without a visible nidus, further complicating the diagnosis. Computed tomography imaging later identified a well-defined nidus in the neck of the fifth metatarsal, confirming osteoid osteoma. Owing to the atypical symptoms, larger lesion size (> 1.5 cm), and poor response to conservative management, the patient underwent curettage and bone grafting, leading to complete symptom resolution. Histopathology confirmed the diagnosis, and postoperative follow-up showed full recovery with no recurrence at 6 months.</p><p><strong>Conclusion: </strong>This case underscores the importance of considering osteoid osteoma in cases of unexplained, persistent metatarsal pain, even in the absence of classical imaging findings and nonsteroidal anti-inflammatory drug responsiveness. Early recognition with advanced imaging, such as computed tomography, is crucial in preventing misdiagnosis and ensuring timely intervention.</p>","PeriodicalId":16236,"journal":{"name":"Journal of Medical Case Reports","volume":"19 1","pages":"427"},"PeriodicalIF":0.8000,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12382063/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Medical Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s13256-025-05366-0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Background: Osteoid osteoma is a benign bone tumor commonly affecting the lower extremities, typically the femur or tibia. However, its occurrence in the fifth metatarsal bone is rare, and atypical presentations can lead to delayed diagnosis and misinterpretation as other pathologies.
Case presentation: We report the case of a 14-year-old Persian male athlete who presented with persistent lateral forefoot pain lasting 2 years, initially attributed to a traumatic injury. The pain was progressively worsening, nocturnal, and unresponsive to nonsteroidal anti-inflammatory drugs, deviating from the classical dramatic relief associated with this tumor. Radiographs initially showed diffuse sclerosis without a visible nidus, further complicating the diagnosis. Computed tomography imaging later identified a well-defined nidus in the neck of the fifth metatarsal, confirming osteoid osteoma. Owing to the atypical symptoms, larger lesion size (> 1.5 cm), and poor response to conservative management, the patient underwent curettage and bone grafting, leading to complete symptom resolution. Histopathology confirmed the diagnosis, and postoperative follow-up showed full recovery with no recurrence at 6 months.
Conclusion: This case underscores the importance of considering osteoid osteoma in cases of unexplained, persistent metatarsal pain, even in the absence of classical imaging findings and nonsteroidal anti-inflammatory drug responsiveness. Early recognition with advanced imaging, such as computed tomography, is crucial in preventing misdiagnosis and ensuring timely intervention.
期刊介绍:
JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect