Open Access
CC BY 4.0 · Arq Neuropsiquiatr 2024; 82(S 01): S1-S52
DOI: 10.1055/s-0044-1789441
Supplement

Analyzing the association between cancer and neuromyelitis optica: a case series

Felipe B. Brunheroto
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Belo Horizonte MG, Brazil.
,
Natália Cirino Talim
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Belo Horizonte MG, Brazil.
,
Juliana Santiago-Amaral
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Belo Horizonte MG, Brazil.
,
Paulo Pereira Christo
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Belo Horizonte MG, Brazil.
,
Marco A. Lana-Peixoto
1   Universidade Federal de Minas Gerais, Faculdade de Medicina, Centro de Investigação de Esclerose Múltipla, Belo Horizonte MG, Brazil.
› Author Affiliations
 

    Address for correspondence: Marco A. Lana Peixoto (email: marco.lanapeixoto@gmail.com).

    Abstract

    Background: Neuromyelitis optica spectrum disorders (NMOSD) are immune-mediated disorders of the central nervous system, with anti-aquaporin 4 antibodies most often detected in serum. The increasing number of reports associating cancer and NMOSD raises questions about their interconnectedness, especially when considering a cross-reactive mechanism of tumor cells triggering autoimmunity.

    Objective: To investigate the prevalence and characteristics of patients with both cancer and NMOSD, to gain insights into those under care at the CIEM MS Research Center.

    Methods: We reviewed the medical records of patients at our center diagnosed with NMOSD with a history of cancer.

    Results: In a cohort of 281 patients with NMOSD, 8 met the established criteria (2.8%); 4 (50%) of them tested positive for anti-AQP-4 antibodies, and 6 (75%) were female subjects. The tumors identified included breast and cervical cancers (25% each), multiple myeloma (12.5%), pheochromocytoma (12.5%), prostate cancer (12.5%), and bladder cancer (12.5%). The patients presented heterogeneous phenotypes, with initial symptoms such as myelitis (62.5%), optic neuritis (50%), area postrema syndrome (50%), and brainstem syndrome (12.5%). Longitudinally-extensive transverse myelitis (LETM) was prominent, occurring in 7 (87.5%) patients, whereas optic neuritis occurred in 6 (75%) subjects.

    Conclusion: Our findings are in line with those reported in the literature, indicating an association pf 3 to 12% between NMOSD and cancer, predominantly in female patients. The most prevalent symptom was LETM. In agreement with other published series, breast and genitourinary cancers were frequently-reported histological types.


    No conflict of interest has been declared by the author(s).

    Publication History

    Article published online:
    02 October 2024

    © 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

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