Evidence map›Paper›PMID 41446470›Full record

ArticleCureus2025

A Rare Presentation of Sphenoid Sinus Lymphoma in an 18-Year-Old Female.

Noor Binsanad, Latifa Fakhroo, Abdulla Darwish, Bedoor Alomran, Mohammed Albalooshi

Abstract readCase Reports
In one paragraph

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

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Noor BinsanadOtolaryngology, Bahrain Defence Force Royal Medical Services, Riffa, BHR.
Latifa FakhrooDiagnostic Radiology, Bahrain Defence Force Royal Medical Services, Riffa, BHR.
Abdulla DarwishPathology and Laboratory Medicine, Bahrain Defence Force Royal Medical Services, Riffa, BHR.
Bedoor AlomranDiagnostic Radiology, Bahrain Defence Force Royal Medical Services, Riffa, BHR.
Mohammed AlbalooshiNeurological Surgery, Bahrain Defence Force Royal Medical Services, Riffa, BHR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sphenoid sinus lymphomas are extremely rare, constituting a small fraction of both sphenoid sinus malignancies and extranodal non-Hodgkin lymphomas. Their clinical presentation can vary widely, ranging from symptoms resembling chronic sinusitis to more severe manifestations such as nerve palsies and visual disturbances. An 18-year-old female with no significant medical history presented with blurred vision, diplopia, and a left-sided headache lasting one week. Neurological examination revealed mild limitation of lateral rectus movement in the left eye. Imaging studies, including non-contrast CT and MRI, identified a hyperdense mass arising from the left sphenoid sinus. A biopsy obtained via a transnasal sphenoidal approach confirmed a diagnosis of pre-B cell lymphoblastic lymphoma. Following the biopsy, the patient was treated with IV dexamethasone, leading to complete resolution of her symptoms and regression of the mass on follow-up imaging. Staging confirmed the diagnosis of stage 1A B-cell lymphoblastic lymphoma. The patient underwent chemotherapy and radiotherapy and remains in remission five years later. However, she developed bilateral hip avascular necrosis as a side effect, requiring hip replacement surgery. Diagnosing sphenoid sinus lymphoma can be challenging due to its nonspecific symptoms and the complex anatomy of the sphenoid sinus, often leading to misdiagnosis as more common conditions such as sinusitis or cranial nerve palsies. Imaging, particularly MRI and CT, plays a critical role in assessing the disease's extent and evaluating potential cranial nerve involvement. A biopsy is essential for obtaining a definitive histological diagnosis to guide appropriate treatment plans. While steroids can offer rapid symptom relief, the primary treatment for sphenoid sinus lymphoma involves chemotherapy, often in combination with radiotherapy. Surgery is typically not recommended due to the tumor's location and potential risks to surrounding structures. The case highlights the importance of considering neoplastic lesions in patients presenting with unexplained headaches and ocular findings to support timely diagnosis.

Indexed as

cranial nerve involvementcranial nerve palsydiplopialymphomaparanasal sinus diseasesparanasal sinus neoplasmpre-b lymphoblastic lymphomasphenoid sinus lesionssphenoid sinus tumor

Identifiers

PMID41446470
PMCPMC12723425

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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 OpenQuestion graph.