Evidence map›Paper›PMID 39802596›Full record

ArticleCase reports in neurological medicine2025

Chronic Myeloid Leukemia Presenting With Bilateral Optic Neuropathy and Sensorineural Hearing Loss as the First Clinical Presentation: A Case Report.

Sameen Ejaz, Rabia Nawaz, Fakeha Tariq, Ahmad Nawaz, Safia Bano, Ayesha Aslam, Fawad Khan, Zeeshan Ahmed, Aaqib Rashid, Sana Saqib

Abstract readCase Reports
In one paragraph

Article in Case reports in neurological medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Sameen EjazDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0008-9879-0747
Rabia NawazDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0001-3679-1858
Fakeha TariqDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0008-5070-0968
Ahmad NawazDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0000-0002-3247-533X
Safia BanoDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0003-3639-7097
Ayesha AslamDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0000-0001-6341-9632
Fawad KhanDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0003-4443-8506
Zeeshan AhmedDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0008-0823-0034
Aaqib RashidDepartment of Neurology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0005-1821-7464
Sana SaqibDepartment of Pathology, Mayo Hospital, King Edward Medical University, Lahore, Pakistan.ORCID https://orcid.org/0009-0000-7668-7329

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chronic myeloid leukemia (CML) is a myeloproliferative disorder that commonly manifests in chronic, accelerated, or blast phase. Typically observed in individuals aged 60-65 years, CML is infrequently diagnosed in adolescents. The usual presentation in late adulthood involves nonspecific symptoms such as fever, fatigue, and weight loss, with rare reports of initial neurological involvement. A 17-year-old male presented with bilateral vision loss and profound hearing loss, alongside a medical history marked by fever, night sweats, and weight loss. A positive tuberculosis contact raised suspicions of tuberculous meningitis, while cervical and inguinal lymphadenopathy suggested the possibility of neurosarcoidosis. Despite clinical signs pointing toward a neurological cause, elevated white blood cell (WBC) count, a bone marrow biopsy, and the identification of BCR-ABL translocation through chromosomal analysis surprisingly revealed a diagnosis of CML in the chronic phase. This case underscores the importance of considering hematological malignancy as a differential in cases of multiple cranial neuropathies, especially if supported by systemic symptoms. Understanding the diverse presentations of CML is essential for clinicians to provide timely and appropriate interventions particularly in young patients where it could mimic other neurological disorders leading to diagnostic challenges and delay in treatment initiation.

Indexed as

adolescentchronic myeloid leukemiacranial neuropathyoptic neuropathysensorineural hearing lossvision loss

Identifiers

PMID39802596
PMCPMC11724030

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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.