Evidence map›Paper›PMID 38742259›Full record

ArticleBrain tumor research and treatment2024

Solitary Skull Langerhans Cell Histiocytosis Presenting With a Pus Draining Fistula: An Unusual Presentation and Review of Literature.

Hafiza Hifza Bashir, Hafiza Fatima Aziz, Faizan Saeed, Muhammad Ehsan Bari, Nasir Uddin

Abstract readCase Reports
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Article in Brain tumor research and treatment, 2024. 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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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Hafiza Hifza BashirLiaquat National Hospital, Karachi, Pakistan. hifzabashir85@gmail.com.ORCID https://orcid.org/0009-0001-6464-0264
Hafiza Fatima AzizSection of Neurosurgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan.
Faizan SaeedSection of Neurosurgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan.
Muhammad Ehsan BariSection of Neurosurgery, Department of Surgery, Aga Khan University Hospital, Karachi, Pakistan.
Nasir UddinDepartment of Pathology and Laboratory Medicine, Aga Khan University Hospital, Karachi, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Langerhans cell histiocytosis (LCH) is a rare condition in adults, especially when it is limited to a single area of the skull, known as solitary calvarial involvement. In this case report, we present a unique instance of LCH affecting the parietal bone with a pus-draining fistula. This is a rare and unusual presentation at this location, which has been scarcely reported in medical literature. A 30-year-old woman with no prior comorbidity presented with complaints of headache that persisted for a year. She also had swelling on her scalp and a yellowish discharge for 3 weeks, but no neurological problems were observed. Radiology revealed thinning of the calvaria, with ragged margins along the inner table, multiple focal erosions, and involvement of overlying soft tissue and bony sequestrum. The patient underwent biparietal craniotomy and excision of the lesion. The histopathology report showed LCH. After 8 months of follow-up, there was no recurrence. The management of solitary calvarial involvement by LCH with masquerading presentation as a scalp infection can be achieved through complete excision of the lesions, resulting in a favorable outcome.

Indexed as

FistulaHistiocytosisInflammationLangerhans-cellSkull

Identifiers

PMID38742259
PMCPMC11096636

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