Evidence map›Paper›PMID 42597848›Full record

ArticleJournal of orthopaedic case reports2026

Surgical Outcome of a Giant Dorsal Spinal Neurofibroma: A Case Report.

Abdullah Al Mahmud, Md Shahidul Islam Akon, Md Hamidul Haque, Md Shafiul Ezaz, Md Solaiman Hasan, Tazin Jahan

Abstract readCase Reports
In one paragraph

Article in Journal of orthopaedic case reports, 2026. 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Abdullah Al MahmudDepartment of Orthopaedic Surgery, Ibn Sina Medical College Hospital, Dhaka, Bangladesh.
Md Shahidul Islam AkonDepartment of Orthopaedic Surgery, Dhaka Medical College Hospital, Dhaka, Bangladesh.
Md Hamidul HaqueDepartment of Orthopaedic Surgery, Ibn Sina Medical College Hospital, Dhaka, Bangladesh.
Md Shafiul EzazDepartment of Orthopaedic Surgery, Ibn Sina Medical College Hospital, Dhaka, Bangladesh.
Md Solaiman HasanDepartment of Orthopaedic Surgery, National Institute of Traumatology and Orthopaedic Rehabilitation (NITOR), Dhaka, Bangladesh.
Tazin JahanDepartment of Surgery, Shaheed Suhrawardy Medical College and Hospital, Dhaka, Bangladesh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Spinal neurofibromas are rare neurogenic tumors that can cause progressive neurological deficits due to spinal cord compression. Early diagnosis and timely surgical intervention are crucial to prevent permanent neurological impairment and restore functional mobility. Case Report: A 38-year-old male presented to Ibn Sina Medical College Hospital with persistent mid-back pain and progressive weakness in both lower limbs, which eventually caused difficulty in independent ambulation. Neurological examination revealed decreased motor strength in the lower limbs (Medical Research Council [MRC] Grade - 4/5), sensory deficit below the D6 dermatome, and exaggerated deep tendon reflexes. Magnetic resonance imaging (MRI) of the thoracic spine demonstrated a large, well-defined, dumbbell-shaped paraspinal mass at the thoracic spine levels 5 and 6 (D5-D6) vertebral level, extending through the intervertebral foramen into the spinal canal with significant spinal cord compression. Based on clinical and radiological findings, a diagnosis of thoracic spinal neurofibroma (dumbbell type) was made. The patient underwent complete surgical excision of the tumor with spinal stabilization under general anesthesia. Intraoperatively, the tumor was encapsulated and extended from the spine to the subcutaneous tissue and right chest wall, destroying the D5-D6 vertebral body, lamina, pedicles, and part of the 5th and 6th ribs. Histopathology confirmed the diagnosis of neurofibroma. Postoperatively, the patient's neurological function gradually improved, and follow-up imaging confirmed complete tumor resection with no residual compression. At 1-month follow-up, he was mobilizing independently, with significant pain relief and no surgical complications. At 4 years follow-up, the patient achieved independent ambulation, and neurological function had returned to normal. Conclusion: Surgical excision with spinal stabilization is an effective treatment for thoracic dumbbell-shaped neurofibromas. Early diagnosis and intervention can lead to excellent neurological recovery, restoration of mobility, and improved quality of life.

Indexed as

back paingiant dorsal spinal neurofibromaSurgical outcome

Identifiers

PMID42597848
PMCPMC13470595

What Socratic holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.