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. 2018 Aug 8;58(3):107–121. doi: 10.3960/jslrt.18011

Table 5. Previous reports of HAM-mimicking myelitis after allo-HSCT and HAM after organ transplantation.

Year HAM Recipient
after OTP
Development of HAM Age, sex Transplantation Recipient
HTLV-1
Donor
HTLV-1
Recipient
HTLV-1
after organ
transplantation
HTLV-1
DNA
Neopterin Immune
suppression
Donor cells Therapy Outcome
Kawamata et al. 2014 HAM-
mimicking
myelitis
- 20 months 63, F BMT + - - - 8 CSP CD4+
CXCR3+
CCR4+
mPSL Imp
Present case 2017 Atypical
HAM
- 5 months 46, F BMT + - - 10.8 copies/
1000 cells)
95 FK+sMTx
→CSP
CD4+
CXCR3+
partially
CCR4+
mPSL Imp
Nagamine et al. 2014 HAM + 2 months 38, F RTP - + + 15/1000(PB) 51 FK/MMF CD4+:54% IFNα Imp
Ramanan et al. 2014 HAM + 5 months 56, M RTP - + + n.d. n.d. FK/MMF
PSL
n.d. PSL
AZT
Imp
Inose et al. 2010 HAM + 10 months 51, M RTP - n.e. + 7.4% n.d. CY/PSL n.d. IFNα Imp
Kuroki et al. 2007 HAM n.e. 17 months 40, M RTP n.e. n.e. n.e. 0.83% n.d. CY/MMF/PSL n.d. PSL Imp
Toro C et al.
Zarranz
Imirizaidu JJ et al.
2003 HAM + 24 months 54, F RTP - + + 12.44%
(164.4/1000)
n.d. CY n.d. PSL PD
Toro C et al.
Zarranz
Imirizaidu JJ et al.
2003 HAM + 20 months 57, M RTP - + + 16.44%
(124.4/1000)
n.d. CY n.d. PSL PD
Nakamura N et al. 2001 HAM + < 1 year 48, M RTP n.e. n.e. + n.d. 121 n.d. n.d. PE Imp
Shintani et al. 2001 HAM + 7 years 56, M RTP n.e. n.e. + n.d. n.d. n.d. n.d. PSL n.d.
Nakatsuji Y et al. 2010 HAM + 4 years 50, M RTP - n.e. + n.d. n.d. CY/MMF/PSL n.d. n.d. n.d.
Kuroda Y et al. 1992 HAM + 11 months 32, M RTP n.e. + + n.d. n.d. CY/MZR
PSL.AZA
n.d. PSL Imp
Soyama A 2008 HAM + 20 months 58, M Liver TRP + + + 180/1000 n.d. TAC/PSL n.d. IFNα
ribavium
unchange
Toro C et al.
Zarranz
Imirizaidu JJ et al.
2003 HAM + 18 months 44, F Liver TRP - + + + n.d. TAC n.d. PSL
IFNα
SD
Ozen S et al. 2001 HAM + 5 months 41, M Heart TRP - - + n.d. n.d. n.d. n.d. PSL Imp

In the present and previous reports of HAM-mimicking myelitis or atypical HAM after allo-HSCT and of HAM after organ transplantation (renal, liver, or heart transplantation), two cases were after allo-HSCT, and 13 cases were after organ transplantation, including 10 cases after renal transplantation, two cases after liver transplantation, and one case after heart transplantation. The majority of cases were donor-derived HAM. The presence of anti-HTLV-1 antibodies, and rapid development and progression of HAM were characteristic of HAM after organ transplantation. In one case after allo-HSCT, HAM-mimicking myelitis developed in the absence of anti–HTLV-1 antibodies and the presence of HTLV-1 proviral DNA, with rapid development and progression of the symptoms. In our case after allo-HSCT, atypical HAM developed in the absence of anti–HTLV-1 antibodies and presence of HTLV-1 proviral DNA, with rapid development and progression of the symptoms.