Prolonged Vancomycin‐Induced Linear IgA Disease in a Patient With Renal Failure

ABSTRACT A 64‐year‐old man with pneumococcal septic shock and subsequent renal failure underwent treatments with antibiotics including intravenous vancomycin (VCM). Blistering skin lesions appeared 10 days after the initiation of VCM. When the patient was transferred to us 5 months later, blisters with erythema were still observed on the abdomen and thighs. Histopathological examination revealed subepidermal blister with infiltration of eosinophils and neutrophils, and direct immunofluorescence revealed linear IgA deposition at the basement membrane zone. The diagnosis of linear IgA disease (LAD)was made, and drug‐induced LAD by VCM was suspected, because of the episode of the blister development 10 days after the first VCM administration. Although the results of various sero‐immunological tests were negative, IgA reactivity with type Ⅶ collagen was detected by VCM‐treated ELISA, which further suggested the diagnosis of VCM‐induced LAD. The possible mechanism for the prolonged disease course was speculated.

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Publication Details

Journal
JEADV Clinical Practice
Published
2025-01-27
DOI
https://doi.org/10.1002/jvc2.622
Primary Topic
Blood disorders and treatments
Type
article
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article

Prolonged Vancomycin‐Induced Linear IgA Disease in a Patient With Renal Failure

Takahiro Kiyohara, Takashi Hashimoto, Kaori Takezawa, Mako Mine et al.
JEADV Clinical Practice
Blood disorders and treatments
article

Prolonged Vancomycin‐Induced Linear IgA Disease in a Patient With Renal Failure

Takahiro Kiyohara, Takashi Hashimoto, Kaori Takezawa, Mako Mine, Reiko Noborio, Yuki Nomura
article en

Abstract

ABSTRACT A 64‐year‐old man with pneumococcal septic shock and subsequent renal failure underwent treatments with antibiotics including intravenous vancomycin (VCM). Blistering skin lesions appeared 10 days after the initiation of VCM. When the patient was transferred to us 5 months later, blisters with erythema were still observed on the abdomen and thighs. Histopathological examination revealed subepidermal blister with infiltration of eosinophils and neutrophils, and direct immunofluorescence revealed linear IgA deposition at the basement membrane zone. The diagnosis of linear IgA disease (LAD)was made, and drug‐induced LAD by VCM was suspected, because of the episode of the blister development 10 days after the first VCM administration. Although the results of various sero‐immunological tests were negative, IgA reactivity with type Ⅶ collagen was detected by VCM‐treated ELISA, which further suggested the diagnosis of VCM‐induced LAD. The possible mechanism for the prolonged disease course was speculated.

JEADV Clinical PracticeVol. 4(2)
Kansai Medical University (JP)
Openalex Percentile: Top 98%
Blood disorders and treatments
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