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. 2019 Feb 4;26:244–247. doi: 10.1016/j.rmcr.2019.02.001

Table 1.

Summary of reported PPFE cases after bone marrow transplantation.

Source Patients Age Sex Underlying disease Manifestation after BMT (years) Histological findings
Present case 1 30 M ALL 16 PPFE, BO, cellular and fibrotic NSIP
Thusen, 2011 [5] 4 13 F AA 2.8 subpleural fibrosis, BO, mild patchy inflammation
23 M AML 12 subpleural and paraseptal fibroelastosis, BO
32 M ALL 16 subpleural fibroelastosis, BO, pneumothorax
55 F AML 2 PPFE, BO, widespread pulmonary fibrosis
Fujikura, 2014 [7] 1 31 F ALL 9 PPFE, BO
Takeuchi, 2015 [6] 20 27.5 (8–57) 11 M
9 F
AML (12)
MDS (2)
ALL (1)
Primary macroglobulinemia (1)
SCID (1)
Aplastic anemia (1)
Chediak-Higashi syndrome (1)
Neuroblastoma (1)
1.2 (0.4–3.8) BO (20)
PPFE (15)
NSIP fibrotic (9)
NSIP cellular (6)
Mariani, 2016 [4] 2 33 M AML 13 PPFE was diagnosed by HRCT
61 F AML 5
Matsui, 2016 [11] 1 40 M HL 2.7 PPFE, diffuse interstitial fibrosis
Ishii, 2016 [8] 5 44 F MDS (RA) 3.3 PPFE, fibrotic lesions, no significant inflammatory cell infiltration
27 M MDS (RA) 1.1
38 M CML 9.1
28 M ALL 6.4
50 M AA 8.8
Cha, 2017 [9] 2 54 M AML 2 PPFE, diffuse lymphocytic infiltration
16 M AML n/a PPFE, BO, patchy lymphocytic infiltration
Okimoto, 2018 [10] 1 45 F MDS 5 PPFE

AA, aplastic anemia.

ALL, acute lymphoblastic leukemia.

AML, acute myeloid leukemia.

BO, bronchiolitis obliterans

BMT, bone marrow transplantation.

CML, chronic myeloid leukemia.

HL, Hodgkin lymphoma.

HRCT, high resolution computed tomography.

MDS, myelodysplastic syndrome.

NSIP, non-specific interstitial pneumonia.

RA, refractory anemia.

SCID, severe combined immunodeficiency.