Mitochondrial–Immune Overlap in Leber Hereditary Optic Neuropathy: A Case Report and Lessons Learned

<b>Background and Clinical Significance</b>: Leber hereditary optic neuropathy (LHON) is a mitochondrial disorder characterized by acute or subacute bilateral central vision loss, typically in young males. Multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) are immune-mediated demyelinating diseases that may present with optic neuritis and myelitis. Although distinct in etiology, recent evidence suggests that mitochondrial dysfunction and neuroinflammation can overlap, giving rise to combined phenotypes such as LHON-MS (also known as Harding's disease). <b>Case Presentation</b>: We report a 42-year-old man who initially presented in 2018 with right-eye pain and severe visual loss diagnosed as idiopathic optic neuritis. Despite corticosteroid and plasma-exchange therapy, visual recovery was poor, and he was maintained on azathioprine. One year later, he developed visual flashes and left-eye visual loss with bilateral optic nerve thinning on OCT. Genetic testing revealed a pathogenic <i>MT-ND4</i> (m.11778G>A) mutation, confirming LHON. In 2021, he presented with ascending lower-limb numbness and bladder urgency. MRI demonstrated a central thoracic cord lesion at T11, consistent with acute transverse myelitis, while serum AQP4 and MOG antibodies were negative. CSF showed five unique oligoclonal bands. The diagnosis of LHON-MS overlap was established, and he was treated with corticosteroids followed by rituximab with clinical stability thereafter. <b>Conclusions</b>: This case highlights the diagnostic challenges of LHON with atypical optic neuritis initially followed by the development of demyelinating disease. Red flags such as poor visual recovery, bilateral or sequential optic neuropathy, and steroid-refractory episodes should prompt genetic testing to rule out LHON. Recognition of the mitochondrial-immune overlap is essential for accurate diagnosis, counseling, and an appropriate therapeutic strategy.

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Journal
Reports — Medical Cases Images and Videos
Published
2025-12-05
DOI
https://doi.org/10.3390/reports8040258
Primary Topic
Mitochondrial Function and Pathology
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article
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Mitochondrial–Immune Overlap in Leber Hereditary Optic Neuropathy: A Case Report and Lessons Learned

Hind Alnajashi, Walid Eltantawi
Reports — Medical Cases Images and Videos
Mitochondrial Function and Pathology
article

Mitochondrial–Immune Overlap in Leber Hereditary Optic Neuropathy: A Case Report and Lessons Learned

Hind Alnajashi, Walid Eltantawi
article en

Abstract

<b>Background and Clinical Significance</b>: Leber hereditary optic neuropathy (LHON) is a mitochondrial disorder characterized by acute or subacute bilateral central vision loss, typically in young males. Multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) are immune-mediated demyelinating diseases that may present with optic neuritis and myelitis. Although distinct in etiology, recent evidence suggests that mitochondrial dysfunction and neuroinflammation can overlap, giving rise to combined phenotypes such as LHON-MS (also known as Harding's disease). <b>Case Presentation</b>: We report a 42-year-old man who initially presented in 2018 with right-eye pain and severe visual loss diagnosed as idiopathic optic neuritis. Despite corticosteroid and plasma-exchange therapy, visual recovery was poor, and he was maintained on azathioprine. One year later, he developed visual flashes and left-eye visual loss with bilateral optic nerve thinning on OCT. Genetic testing revealed a pathogenic <i>MT-ND4</i> (m.11778G>A) mutation, confirming LHON. In 2021, he presented with ascending lower-limb numbness and bladder urgency. MRI demonstrated a central thoracic cord lesion at T11, consistent with acute transverse myelitis, while serum AQP4 and MOG antibodies were negative. CSF showed five unique oligoclonal bands. The diagnosis of LHON-MS overlap was established, and he was treated with corticosteroids followed by rituximab with clinical stability thereafter. <b>Conclusions</b>: This case highlights the diagnostic challenges of LHON with atypical optic neuritis initially followed by the development of demyelinating disease. Red flags such as poor visual recovery, bilateral or sequential optic neuropathy, and steroid-refractory episodes should prompt genetic testing to rule out LHON. Recognition of the mitochondrial-immune overlap is essential for accurate diagnosis, counseling, and an appropriate therapeutic strategy.

Reports — Medical Cases Images and VideosVol. 8(4)
King Abdulaziz University (SA), King Abdullah International Medical Research Center (SA), King Abdulaziz Hospital (SA)
Openalex Percentile: Top 65%
Mitochondrial Function and Pathology
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