Evidence map›Paper›PMID 41281881›Full record

ArticleJournal of orthopaedic case reports2025

Management of Solitary Osteochondroma Arising from Mammillary Process of D12 Vertebra in an 11-Year-Old Female: A Rare Case Report and Literature Review.

Rajnand Kumar, Nitish Kumar, Vivek Kumar, Sudhir Shyam Kushwaha, Ajay Bharti

Abstract readCase Reports
In one paragraph

Article in Journal of orthopaedic case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Rajnand KumarDepartment of Orthopedics, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.
Nitish KumarDepartment of Orthopedics, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.
Vivek KumarDepartment of Orthopedics, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.
Sudhir Shyam KushwahaDepartment of Orthopedics, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.
Ajay BhartiDepartment of Orthopedics, All India Institute of Medical Sciences, Gorakhpur, Uttar Pradesh, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Osteochondromas are benign bony lesions arising from the metaphysis of long bones, commonly arising from the distal femur, proximal tibia, and proximal humerus, with rare incidence of its presence over the flat bones such as the scapula and pelvis. The spine can be rarely affected by osteochondromas in 1-4% of all cases. The origin of osteochondroma from the mammillary process of the D12 vertebra is very rare. Hence, we are reporting this rare phenomenon. Case Report: An 11-year-old female presented with the complaints of gradually progressive swelling in the mid-back region with discomfort on lying down in the supine position. Based on clinical and radiological findings, a provisional diagnosis of osteochondroma arising from D12 vertebrae was made and planned for excisional biopsy under general anesthesia. Histopathology of the excised bone mass was consistent with osteochondroma. The patient was followed for 1 year, in which no signs of recurrence were found, and she was carrying out her activities of daily living without any discomfort. Conclusion: Osteochondroma of D12 is a rare phenomenon, but it should also be kept as a differential diagnosis while treating patients with unexplained back symptoms in a normal X-ray. Surgical excision should be kept reserved for large osteochondromas outside of the neural canal or tumors causing neural symptoms.

Indexed as

dorsal spineOsteochondromaspinal osteochondroma

Identifiers

PMID41281881
PMCPMC12636854

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