Evidence map›Paper›PMID 42559333›Full record

ArticleSurgical neurology international2026

Giant scalp malignant peripheral nerve sheath tumor with bone involvement: Case report and review of the literature.

Kunal Singla, Nishant Goyal, Puspendu Chakraborty, Shrutika Chopra, Ravi Hari Phulware

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In one paragraph

Article in Surgical neurology international, 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

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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

5 authors.

Kunal SinglaDepartment of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Nishant GoyalDepartment of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Puspendu ChakrabortyDepartment of Neurosurgery, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.
Shrutika ChopraPathology and Laboratory Medicine, Sri Guru Ram Das Institute of Medical Sciences and Research, Amritsar, Punjab, India.
Ravi Hari PhulwarePathology and Laboratory Medicine, All India Institute of Medical Sciences, Rishikesh, Uttarakhand, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Malignant peripheral nerve sheath tumors (MPNSTs) constitute a group of malignant neoplasms with neuroectodermal origin. MPNSTs are rare, with an expected incidence of 0.1/100,000 per year. Occurrences of MPNSTs on the scalp are exceptionally rare, with only 26 cases involving the scalp reported in the published literature. We wish to report a rare case of giant scalp MPNST and discuss the management options of this rare entity, along with the literature review pertaining to the same. Case Description: A 50-year-old male presented with a firm to hard swelling on the top of his head for the past 8 months. Magnetic resonance imaging showed an extra-axial, transcalvarial heterogeneously enhancing lesion of size 10 cm × 9 cm × 7 cm in the midline in the frontoparietal convexity. The patient underwent bi-frontal craniectomy with gross total resection of the tumor mass with titanium mesh cranioplasty. His postoperative period was uneventful, and he was discharged on the 7 Conclusion: The cases of MPNST should be treated by resection of the affected bone and cranioplasty followed by radiation therapy. Chemotherapy is reserved for high-grade lesions with distant metastasis. The overall survival rate for these highly aggressive tumors is frequently restricted, with a reported figure of approximately 30% over 5 years.

Indexed as

Hump on headMalignant peripheral nerve sheath tumorNeurofibromaScalp swelling

Identifiers

PMID42559333
PMCPMC13440753

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