Intravenous immunoglobulin-induced, non-eczematous, vesiculobullous eruptions in Stevens-Johnson syndrome.Am J Clin Dermatol. 2009; 10(5):339-42.AJ
Abstract
Intravenous immunoglobulin (IVIG) has emerged as a promising treatment that interrupts the progression of Stevens-Johnson syndrome (SJS). Our patient experienced an uncommon adverse effect, non-eczematous, vesiculobullous eruptions, after treatment with IVIG. These new lesions developed rapidly on the palms while most previous SJS bullous lesions subsided. A skin biopsy of these new lesions showed an intracorneal vesicle, without epidermal necrosis, with inflammatory cell infiltration. IVIG-induced, vesiculobullous eruptions are discussed, along with their possible pathogenesis. With the increasing use of IVIG for treatment of bullous dermatoses, recognition of this rare adverse effect is important for prompt differential diagnosis.
Links
MeSH
Pub Type(s)
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
19658448
Citation
Lin, Wan-Lung, et al. "Intravenous Immunoglobulin-induced, Non-eczematous, Vesiculobullous Eruptions in Stevens-Johnson Syndrome." American Journal of Clinical Dermatology, vol. 10, no. 5, 2009, pp. 339-42.
Lin WL, Lin WC, Chang YC, et al. Intravenous immunoglobulin-induced, non-eczematous, vesiculobullous eruptions in Stevens-Johnson syndrome. Am J Clin Dermatol. 2009;10(5):339-42.
Lin, W. L., Lin, W. C., Chang, Y. C., Yang, L. C., Hung, S. I., Hong, H. S., & Chung, W. H. (2009). Intravenous immunoglobulin-induced, non-eczematous, vesiculobullous eruptions in Stevens-Johnson syndrome. American Journal of Clinical Dermatology, 10(5), 339-42. https://doi.org/10.2165/11310610-000000000-00000
Lin WL, et al. Intravenous Immunoglobulin-induced, Non-eczematous, Vesiculobullous Eruptions in Stevens-Johnson Syndrome. Am J Clin Dermatol. 2009;10(5):339-42. PubMed PMID: 19658448.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Intravenous immunoglobulin-induced, non-eczematous, vesiculobullous eruptions in Stevens-Johnson syndrome.
AU - Lin,Wan-Lung,
AU - Lin,Wen-Chi,
AU - Chang,Ya-Ching,
AU - Yang,Li-Cheng,
AU - Hung,Shuen-Iu,
AU - Hong,Hong-Shang,
AU - Chung,Wen-Hung,
PY - 2009/8/8/entrez
PY - 2009/8/8/pubmed
PY - 2009/10/14/medline
SP - 339
EP - 42
JF - American journal of clinical dermatology
JO - Am J Clin Dermatol
VL - 10
IS - 5
N2 - Intravenous immunoglobulin (IVIG) has emerged as a promising treatment that interrupts the progression of Stevens-Johnson syndrome (SJS). Our patient experienced an uncommon adverse effect, non-eczematous, vesiculobullous eruptions, after treatment with IVIG. These new lesions developed rapidly on the palms while most previous SJS bullous lesions subsided. A skin biopsy of these new lesions showed an intracorneal vesicle, without epidermal necrosis, with inflammatory cell infiltration. IVIG-induced, vesiculobullous eruptions are discussed, along with their possible pathogenesis. With the increasing use of IVIG for treatment of bullous dermatoses, recognition of this rare adverse effect is important for prompt differential diagnosis.
SN - 1175-0561
UR - https://www.unboundmedicine.com/medline/citation/19658448/Intravenous_immunoglobulin_induced_non_eczematous_vesiculobullous_eruptions_in_Stevens_Johnson_syndrome_
L2 - https://dx.doi.org/10.2165/11310610-000000000-00000
DB - PRIME
DP - Unbound Medicine
ER -