Case report: A co-existing case of ulcerative colitis and dysferlinopathy in a male patient

Patients with inflammatory bowel disease (IBD) are at risk of developing malnutrition, severe dystrophic muscle weakness, and muscle atrophy. We present a case of a 33-year-old male patient who exhibited concurrent muscle atrophy, muscle weakness, diarrhea, and mucopurulent bloody stools. Notably, the patient reported that his household or family members experienced similar symptoms of muscle weakness, without any apparent neurological or psychiatric manifestations. The patient's intestinal symptoms were most consistent with ulcerative colitis, while the muscle weakness originated from dysferlinopathy following a comprehensive diagnostic work-up. The patient was initiated on vedolizumab therapy and L-carnitine therapy, and his symptoms improved after 1 month of follow-up. This case study underscores the necessity for clinicians to maintain a high level of suspicion for the presence of concomitant diseases when encountering IBD patients with muscle weakness. This approach is essential for achieving an early diagnosis and treatment.

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Publication Details

Journal
Frontiers in Medicine
Published
2025-01-22
DOI
https://doi.org/10.3389/fmed.2024.1481780
Primary Topic
Inflammatory Myopathies and Dermatomyositis
Type
article
Field-Weighted Citation Impact
0.00

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article

Case report: A co-existing case of ulcerative colitis and dysferlinopathy in a male patient

Qiong Yan, Mingming Deng, Muhan Lü, Limin Li et al.
1 links
Frontiers in Medicine
Inflammatory Myopathies and Dermatomyositis
article

Case report: A co-existing case of ulcerative colitis and dysferlinopathy in a male patient

Qiong Yan, Mingming Deng, Muhan Lü, Limin Li, Tiejun Zhou, Xiaolin Zhong
article en

Abstract

Patients with inflammatory bowel disease (IBD) are at risk of developing malnutrition, severe dystrophic muscle weakness, and muscle atrophy. We present a case of a 33-year-old male patient who exhibited concurrent muscle atrophy, muscle weakness, diarrhea, and mucopurulent bloody stools. Notably, the patient reported that his household or family members experienced similar symptoms of muscle weakness, without any apparent neurological or psychiatric manifestations. The patient's intestinal symptoms were most consistent with ulcerative colitis, while the muscle weakness originated from dysferlinopathy following a comprehensive diagnostic work-up. The patient was initiated on vedolizumab therapy and L-carnitine therapy, and his symptoms improved after 1 month of follow-up. This case study underscores the necessity for clinicians to maintain a high level of suspicion for the presence of concomitant diseases when encountering IBD patients with muscle weakness. This approach is essential for achieving an early diagnosis and treatment.

Frontiers in MedicineVol. 11
Affiliated Hospital of Southwest Medical University (CN)
National Natural Science Foundation of China
Zero hunger
Openalex Percentile: Top 98%
Inflammatory Myopathies and Dermatomyositis
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