# Marchiafava–Bignami Disease and Pellagra in a Chronic Alcohol User: A Reversible Case of Cognitive Impairment

**Authors:** Diogo Ramos, André Valente, Rodrigo Leão, Ana M Serrano

PMC · DOI: 10.7759/cureus.102149 · 2026-01-23

## TL;DR

A chronic alcohol user showed reversible cognitive and skin issues due to Marchiafava-Bignami disease and pellagra, which improved with vitamin therapy and abstinence.

## Contribution

This case highlights the reversible nature of combined MBD and pellagra in alcohol users through early diagnosis and treatment.

## Key findings

- MRI showed corpus callosum demyelination consistent with MBD.
- Niacin deficiency confirmed through lab tests, indicating pellagra.
- Cognitive and dermatologic symptoms improved significantly after six months of treatment.

## Abstract

Marchiafava-Bignami disease (MBD) is a rare complication of chronic alcoholism characterized by demyelination of the corpus callosum. Pellagra, resulting from niacin (vitamin B3) deficiency, typically presents with dermatitis, diarrhea, and dementia. Both MBD and pellagra are often associated with severe nutritional deficiencies. We describe the case of a 56-year-old man with alcohol use disorder admitted after a syncopal episode, presenting with disorientation, apathy, and photosensitive desquamative lesions on sun-exposed skin. Brain MRI revealed T2 hyperintensity in the splenium and body of the corpus callosum, compatible with subacute MBS. Laboratory tests confirmed niacin deficiency, establishing concomitant pellagra. The patient received B-complex vitamin supplementation and was maintained in alcohol abstinence. His cognitive and dermatologic condition improved markedly, with near-complete recovery after six months. This case underlines the importance of recognizing nutritional deficiencies in alcohol-related neuropsychiatric presentations.

## Linked entities

- **Chemicals:** niacin (PubChem CID 938)
- **Diseases:** Marchiafava-Bignami disease (MONDO:0016370), pellagra (MONDO:0019975)

## Full-text entities

- **Genes:** GGT1 (gamma-glutamyltransferase 1) [NCBI Gene 2678] {aka CD224, D22S672, D22S732, GGT, GGT 1, GGTD}
- **Diseases:** Executive dysfunction (MESH:D006331), vasovagal (MESH:D019462), dementia (MESH:D003704), macrocytic anemia (MESH:D000748), depression (MESH:D003866), impulsivity (MESH:D007174), desquamative lesions (MESH:C562470), atrophy of the corpus callosum (MESH:D061085), coma (MESH:D003128), Cognitive Impairment (MESH:D003072), erythema (MESH:D004890), malnutrition (MESH:D044342), niacin deficiency (MESH:D007153), myoclonus (MESH:D009207), demyelinating disorder (MESH:D003711), encephalopathy (MESH:D001927), brain injury (MESH:D001930), brain damage (MESH:D001925), thiamine deficiency (MESH:D013832), dermatologic lesions (MESH:D000168), weight loss (MESH:D015431), toxicity (MESH:D064420), dehydration (MESH:D003681), aphasia (MESH:D001037), niacin (vitamin B3) deficiency (OMIM:120050), neurocognitive disorders (MESH:D019965), MBD (MESH:D054319), chronic alcoholism (MESH:D006519), deficits in attention, memory, and executive function (MESH:D001289), neuropsychiatric (MESH:C000631768), thrombocytopenia (MESH:D013921), delirium (MESH:D003693), dermatitis (MESH:D003872), confusion (MESH:D003221), diarrhea (MESH:D003967), cutaneous lesions (MESH:D009059), MBS (MESH:C535807), impaired encoding, (MESH:C564021), seizure (MESH:D012640), neurological deficits (MESH:D009461), dysexecutive syndrome (MESH:D013577), Skin lesions (MESH:D012871), Pellagra (MESH:D010383), Alcohol User (MESH:D000437), gastrointestinal symptoms (MESH:D012817), syncopal episode (MESH:D013575), impaired comprehension (MESH:D001308), anomia (MESH:D000849), atrophy of (MESH:D001284), anxiety (MESH:D001007), behavioral disturbances (MESH:D001523), weakness (MESH:D018908)
- **Chemicals:** cyanocobalamin (MESH:D014805), glucose (MESH:D005947), folic acid (MESH:D005492), Alcohol (MESH:D000438), B-complex vitamin (-), niacin (MESH:D009525), thiamine (MESH:D013831), vitamin B3 (MESH:D009536), pyridoxine (MESH:D011736)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12925483/full.md

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Source: https://tomesphere.com/paper/PMC12925483