| Literature DB >> 26619833 |
Minoru Kojima1, Akitada Ichinose2,3, Masayoshi Souri4,5, Tsukasa Osaki4,5, Hidetsugu Kawai1, Jun Amaki1, Hiroki Numata1, Mitsuki Miyamoto1, Daisuke Ogiya1, Kosuke Tsuboi6, Yoshiaki Ogawa1, Soji Ozawa7, Kiyoshi Ando1.
Abstract
Autoimmune hemorrhaphilia due to anti-factor XIII (FXIII) antibodies (AH13) is a life-threatening disease associated with high risk of surgical bleeding. Since AH13 occurs mainly in the elderly, patients of AH13 tend to be complicated with other life-threatening diseases that may require surgical procedures. During our nation-wide survey on AH13, supported by the Japanese Ministry of Health, Labor, and Welfare, patients with unexplained bleeding were examined for FXIII-related parameters and anti-FXIII autoantibodies. A 64-year-old man had previously been tentatively diagnosed with AH13 and received immunosuppressive therapies, as FXIII inhibitor was detected by functional cross-mixing studies. About 2 years later, he was definitively diagnosed with AH13, because our immuno-chromatographic test and enzyme-linked immuno-sorbent assay detected FXIII-bound anti-FXIII-A subunit autoantibodies. Since routine endoscopic examination revealed suspected esophageal carcinoma, a preparatory FXIII pharmacokinetic (PK) analysis was performed by infusing FXIII concentrates prior to biopsy. Consequently, biopsy of this lesion was done without bleeding complications. One month later, a second PK study was carried out before surgery, and esophageal bypass surgery was completed successfully under FXIII replacement therapy. Our experience with this case suggests that operations can be performed safely and with confidence even in patients with such life-threatening hemorrhagic diseases.Entities:
Keywords: Anti-FXIII/13 antibodies; Autoimmune/acquired hemorrhaphilia; Factor XIII concentrates; Immunosuppressive therapy; Pharmacokinetic study
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Year: 2015 PMID: 26619833 DOI: 10.1007/s12185-015-1917-7
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490