【抗mda5抗体阳性的异基因造血细胞移植后快速进行性间质性肺病经三联免疫抑制治疗成功】。

Yuhei Nakamura, Shunto Kawamura, Shimpei Matsumi, Kazuhisa Matsumoto, Satona Tanaka, Takuto Ishikawa, Akari Matsuoka, Tomohiro Meno, Masakatsu Kawamura, Junko Takeshita, Nozomu Yoshino, Kazuki Yoshimura, Yukiko Misaki, Ayumi Gomyo, Yosuke Okada, Masaharu Tamaki, Machiko Kusuda, Yu Akahoshi, Kazuaki Kameda, Hidenori Wada, Shun-Ichi Kimura, Hideki Nakasone, Shinichi Kako, Hiroshi Date, Yoshinobu Kanda
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He did not have severe graft-versus-host disease, but he developed interstitial pneumonia six months after transplantation when his oral cyclosporine A (CsA) dose was reduced to 10 mg/day. He was given prednisolone (PSL), which temporarily improved his respiratory condition, but he quickly deteriorated when PSL was reduced. Anti-MDA5 antibody was found to be positive after additional testing, and a three-drug combination of intravenous cyclophosphamide+PSL+CsA was initiated for anti-MDA5 antibody positive rapidly progressive interstitial lung disease, which was effective for interstitial pneumonia. He received a successful living-donor lung transplant from his younger brother and sister. 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引用次数: 0

摘要

一名首次完全缓解的34岁KMT2A-MLLT1急性髓系白血病患者在接受了布磺胺/环磷酰胺治疗后,接受了来自hla匹配的姐姐的异体外周血干细胞移植。他没有严重的移植物抗宿主病,但在移植后6个月,当口服环孢素A (CsA)剂量减少到10mg /天时,他出现了间质性肺炎。他被给予强的松龙(PSL),这暂时改善了他的呼吸状况,但当PSL减少时,他迅速恶化。经进一步检测发现抗mda5抗体阳性,开始静脉注射环磷酰胺+PSL+CsA三药联合治疗抗mda5抗体阳性的快速进展性间质性肺病,对间质性肺炎有效。他成功地从弟弟和妹妹那里接受了活体肺移植手术。我们报告一例快速进展的抗mda5抗体阳性间质性肺病患者,在三联治疗和随后的活体供体肺移植后,患者的呼吸状况得到改善。
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[Anti-MDA5 antibody-positive rapidly progressive interstitial lung disease after allogeneic hematopoietic cell transplantation successfully treated with triple immunosuppressive therapy].

A 34-year-old man with KMT2A-MLLT1 acute myeloid leukemia in first complete remission underwent allogeneic peripheral blood stem cell transplantation from his HLA-matched sister after conditioning with busulfan/cyclophosphamide. He did not have severe graft-versus-host disease, but he developed interstitial pneumonia six months after transplantation when his oral cyclosporine A (CsA) dose was reduced to 10 mg/day. He was given prednisolone (PSL), which temporarily improved his respiratory condition, but he quickly deteriorated when PSL was reduced. Anti-MDA5 antibody was found to be positive after additional testing, and a three-drug combination of intravenous cyclophosphamide+PSL+CsA was initiated for anti-MDA5 antibody positive rapidly progressive interstitial lung disease, which was effective for interstitial pneumonia. He received a successful living-donor lung transplant from his younger brother and sister. We present a case of rapidly progressive anti-MDA5 antibody positive interstitial lung disease in which the patient's respiratory condition improved after triple therapy and subsequent living-donor lung transplantation.

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