Table 3.
Vitiligo and/or AA | ||||||||
---|---|---|---|---|---|---|---|---|
Source, Year | Patient Sex/Age, y | Donor Sex | Disease | Transplant Conditioning | Condition | Time to Occurrencea | Distribution | Type of Skin GvHD |
Nagler et al,13 1996 | M/14 | NR | SAA | TLI/Cyc | Vitiligo | 3 mo | Total leukoderma, leukotrichia | cGvHD-Lich |
Aubin et al,7 2000 | M/44 | F | CML | Cyc/Thiotepa/TBI | Vitiligo | 5 mo | Generalized | cGvHD-Lich |
Au et al,6 2001 | M/35 | NR | CML | NR | Vitiligo | 3 y | Generalized, leukotrichia | aGvHD grade 4 |
F/36 | NR | ALL | NR | Vitiligo | 3–5 y | Generalized | aGvHD grade 3 | |
Jacobsohn et al,11 2002 | M/14 | NR | CML | Bu/Ara-C/TBI | Vitiligo | 5 mo | Total leukoderma, leukotrichia | cGvHD-Lich |
Sanli et al,19 2004 | M/26 | NR | AML | Bu/Cyc | AA | 6 mo | Left parietal, vertex, lateral right eyebrow | cGvHD-Lich |
M/19b | NR | CML | Bu/Cyc | Vitiligo and AA | 8 mo | Vitiligo: face, neck, trunk, UE/LE; AA: temporal/occipital | NR | |
M/31 | NR | CML | Bu/Cyc | AA | 3 mo | Eyebrows, forearms | NR | |
Cho et al,9 2005 | M/15 | NR | ALL | Cyc/TBI | Vitiligo | 3 mo | Generalized | aGvHD |
M/30 | F | CML | Cyc/TBI | Vitiligo | 2 y | Generalized | aGvHD | |
M/28 | F | ALL | Cyc/TBI | Vitiligo | 26 mo | Generalized | cGvHD-Scl | |
M/43 | F | MDS | Bu/TBI/Cyc | Vitiligo | 3 mo | Face, UE | cGvHD | |
Williams et al,17 2008 | M/55 | NR | MDS | NR | Vitiligo | 3 y | Total leukoderma, leukotrichia | cGvHD-Epid |
M/66 | NR | MDS | RIC | Vitiligo | 3 y | Generalized | cGvHD | |
Cathcart and Marrell,8 2007 | M/15 | M | FA/AML | Flu/TBI/Cyc/AT G | Vitiligo | 4 y | Hands, arms, neck, trunk, genitalia | aGvHD |
Sanli etal,18 2008 | M/34 | M | CML | Bu/Cyc | Vitiligo | 4 y | Generalized, leukotrichia | cGvHD-Lich |
M/19b | M | CML | Bu/Cyc | Vitiligo and AA | 8 mo | AA: temporal, occipital; Vitiligo: face, neck, trunk, UE/LE | NR | |
M/44 | F | CML | Bu/Cyc | Vitiligo | 7 mo | Face, hair, eyelids, trunk, UE/LE | cGvHD-Fol | |
M/44 | F | CML | Bu/Cyc | Vitiligo | 4 yc | Face, dorsum of hands | cGvHD-Scl | |
F/41 | M | CML | Bu/Flu | Vitiligo | 6 mo | Face | NR | |
Heath et al,10 2009 | F/2 | NR | SCID | Bu/Cyc/ATG | Vitiligo | 4 mo | Chest, arms, legs, face, scalp | aGvHD |
M/5 | NR | X-SCID | Bu/Cyc | Vitiligo | NR | Diffuse depigmentation, scattered leukotrichia | aGvHD | |
Lee etal,12 2009 | M/23 | F | SAA | Cyc | Vitiligo | 2 y | Face, trunk, UE/LE | NR |
Tan et al,16 2011 | F/48 | M | MDS | Cyc/Bu | Vitiligo | 5 yd | Face, trunk, UE/LE | cGvHD-Lich, Scl |
Kamińska et al,20 2012 | M/38 | NR | aApAn | Flu/Alemtuzumab/Mel | AA | 6 mo | Diffuse alopecia | cGvHD |
Oh and Lee,15 2013 | F/36 | NR | ALCL | NR | Vitiligo | 3 wk | UE/LE, trunks | NR |
Nambudiri et al,14 2013 | M/15 | F | X-SCID | None | Vitiligo | 1 mo | Total leukoderma, leukotrichia | cGvHD-Scl |
Abbreviations: AA, alopecia areata; aApAn, acquired aplastic anemia; aGvHD, acute graft-vs-host disease; ALCL, anaplastic large cell lymphoma; ALL, acute lymphoblastic leukemia; AML, acute myelogenous leukemia; Ara-C, cytarabine; ATG, antithymocyte globulin; Bu, busulfan; cGvHD, chronic graft-vs-host disease; CML, chronic myelogenous leukemia; Cyc, cyclophosphamide; Epid, epidermal; FA, Fanconi anemia; Flu, fludarabine; HSCT, hematopoietic stem cell transplantation; LE, lower extremities; Lich, lichenoid; MDS, myelodysplastic syndrome; Mel, melphalan; NR, not reported; RIC, reduced-intensity conditioning; SAA, severe aplastic anemia; SCID, severe combined immunodeficiency; Scl, sclerotic; TBI, total body irradiation; TLI, total lymph node irradiation; UE, upper extremities; X-SCID, x-linked SCID.
Indicates time from allogeneic HSCT to onset of vitiligo or AA.
The case by Sanli et al 2008 may represent the same patient as the 19-year-old patient in Sanli et al 2004.
The donor (sister) of this patient had generalized vitiligo for 10 y. The authors postulate that the development of vitiligo 4 years after transplant was not likely from passive donor transfer.
This patient received 2 allogeneic HSCTs; the time shown refers to time after the second allogeneic HSCT.