2011
DOI: 10.1111/j.1365-2230.2011.04219.x
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Progression of IgA gammopathy to myeloma following infliximab treatment for pyoderma gangrenosum

Abstract: Pyoderma gangrenosum (PG) may be associated with inflammatory disorders and haematological conditions such as monoclonal gammopathy of uncertain significance (MGUS). We report the case of a 53-year old man who had PG and MGUS. After treatment with infliximab for the PG, he developed myeloma. The course of events in this case suggests that infliximab facilitated the progression from MGUS to myeloma.

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Cited by 12 publications
(5 citation statements)
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“…A total of 3212 unique citations were found. 1286 and 1704 citations were excluded by abstract and full‐text read, respectively, yielding 222 articles…”
Section: Resultsmentioning
confidence: 99%
“…A total of 3212 unique citations were found. 1286 and 1704 citations were excluded by abstract and full‐text read, respectively, yielding 222 articles…”
Section: Resultsmentioning
confidence: 99%
“…The severity of MM did not change during adalimumab therapy. Another case presented progression from underlying MGUS to myeloma, following infliximab treatment for pyoderma gangrenosum 19. Therefore, further studies on the relationship between TNF-α blockage and MM progression are required.…”
Section: Discussionmentioning
confidence: 99%
“…However, there is no study reporting the meaning of MM Ig subtype in CD patients. Shareef et al19 reported a case of progression from underlying IgA subtype MGUS to myeloma, following infliximab treatment for pyoderma gangrenosum, and not for CD. However, this case was different from our case, as pre-existing IgA gammopathy progression to myeloma rather than IgA subtype myeloma was caused by infliximab.…”
Section: Discussionmentioning
confidence: 99%
“…Biological agents, like infliximab, show promising efficacy with PG. However, their use should be restricted in patients with monoclonal gammopathy since biological agents may promote flare-up of M-protein [ 165 , 166 ]. Mycophenolate mofetil, cyclophosphamide, danazol, IL-1 inhibitors (anakinra and canakinumab), and azathioprine are options for patients with refractory PG [ 167 169 ].…”
Section: Group IImentioning
confidence: 99%