Fatal occurrence of acquired haemophilia A in a patient with pemphigus vulgaris
R. Maglie L. Quintarelli I. Lastrucci S. Senatore F. Montefusco N. Pimpinelli E. Antiga
First published: 10 June 2019 https://doi.org/10.1111/ced.14022
This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1111/ced.14022
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Abstract
Autoimmune blistering dermatoses (AIBD) and acquired haemophilia A (AHA) are autoimmune conditions that may rarely co‐exist. Recently, Wernham et al. described an interesting case of recalcitrant pemphigus foliaceus complicated by AHA, emphasising the importance of the early detection of AHA because of its life‐threatening behaviour 1. Indeed, we would like to share our experience on a fatal occurrence of AHA in a patient with a well‐controlled pemphigus vulgaris (PV).
R. Maglie L. Quintarelli I. Lastrucci S. Senatore F. Montefusco N. Pimpinelli E. Antiga
First published: 10 June 2019 https://doi.org/10.1111/ced.14022
This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1111/ced.14022
ePDFPDFTOOLS SHARE
Abstract
Autoimmune blistering dermatoses (AIBD) and acquired haemophilia A (AHA) are autoimmune conditions that may rarely co‐exist. Recently, Wernham et al. described an interesting case of recalcitrant pemphigus foliaceus complicated by AHA, emphasising the importance of the early detection of AHA because of its life‐threatening behaviour 1. Indeed, we would like to share our experience on a fatal occurrence of AHA in a patient with a well‐controlled pemphigus vulgaris (PV).
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