TY - JOUR T1 - <span hwp:id="article-title-1" class="article-title"/><span hwp:id="article-title-2" class="sub-article-title">Coexistent Wegener’s Granulomatosis and Goodpasture’s Disease: What Is the Mechanism?</span><span hwp:id="article-title-8" class="sub-article-title">Dr. Humphrey-Murto and Dr. Mulpuru reply</span> JF - The Journal of Rheumatology JO - J Rheumatol SP - 2085 LP - 2085 DO - 10.3899/jrheum.101213.C1 VL - 38 IS - 9 AU - JAE IL SHIN AU - SUSAN HUMPHREY-MURTO AU - SE JIN PARK AU - JI HONG KIM AU - SUNITA MULPURU Y1 - 2011/09/01 UR - http://www.jrheum.org/content/38/9/2085.abstract N2 - Shin JI, Park SJ, Kim JH. Coexistent Wegener’s granulomatosis and Goodpasture’s disease: What is the mechanism? J Rheumatol 2011;38:1521. In the July 2011 issue, a reply was not published for the Letter to the Editor titled “Coexistent Wegener’s Granulomatosis and Goodpasture’s Disease: What Is the Mechanism?”; the letter and reply are given in full below. We regret the error. Coexistent Wegener’s Granulomatosis and Goodpasture’s Disease: What Is the Mechanism? To the Editor: We read with interest the article by Mulpuru, et al1. They described a 50-year-old woman who developed Goodpasture’s disease one month after the diagnosis of Wegener’s granulomatosis1. As one of the possible mechanisms, they described that antineutrophil cytoplasmic antibody … Address correspondence to Dr. Mulpuru; E-mail: sunitamulpuru{at}hotmail.com ER -