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Table 1 Summary of the clinicopathologic features of T-cell lymphoproliferative disorder following autologous hematopoietic stem cell transplantation

From: T-cell lymphoma with a granulomatous lesion of the lungs after autologous hematopoietic stem cell transplantation for Epstein–Barr virus-positive diffuse large B-cell lymphoma: a unique rare case of metachronous B-cell and T-cell lymphoma

 

Age at onset of first neoplasm

Histological diagnosis of first neoplasm

Therapy before AutoHSCT

Histological diagnosis of T-cell LPD

Histological findings

EBV (ISH or PCR)

Areas of T-cell LPD

Time of T-cell LPD onset after HSCT

Outcome

Reference

1

48 years

HL

(1) Doxorubicin-based chemotherapy

(2) High-dose cytosine arabinoside

(3) Conditioning regimen that included cyclophosphamide, etoposide, and ranimustine

T-cell PTLD

(Lymph node) Lymphoid hyperplasia with mild sinus histiocytosis, as well as proliferation of epithelioid cells.

Positive

Mesenteric lymph nodes

2 years and

6 months

Fatal

[12]

2

61 years

AITL

(1) Four cycles of CHOP

(2) High-dose etoposide

(3) Two cycles of CHOP

(4) Ranimustine, cyclophosphamide, etoposide, and carboplatin

T-LGL

(Blood) Pronounced lymphocytosis of large-sized lymphoid cells with round to indented nuclei, coarse chromatin, and azurophilic cytoplasmic granules.

Negative

Bone marrow

1 month

Survival

[13]

3

62 years

FL

(1) Eight cycles of CHOP

(2) Two cycles of MINE

(3) Etoposide

(4) Ranimustine, carboplatin, etoposide, and cyclophosphamide

AITL

(Lymph node) Diffuse infiltration of medium to large-sized lymphoid cells with predominant proliferation of small blood vessels.

Positive

Cervical and supraclavicular lymph nodes

4 months

Resolved

[14]

4

49 years

AITL

(1) Five cycles of CHOP

(2) Salvage chemotherapy: ESHAP

(3) MCVAC

T-cell PTLD

(Autopsy) Lymphoid cells in the bone marrow, portal area of the liver, lymph nodes and lungs.

The hypocellularity in the marrow with the proliferation of macrophages and marked hemophagocytosis.

Macrophages in the marrow, liver, lymph nodes, and lungs.

Positive

Bone marrow, liver, lungs, lymph nodes

3 months

Fatal

[15]

5

47 years

DLBCL

High-dose radiotherapy and chemotherapy

Enteropathy type T-cell lymphoma

(Jejunum) An atypical destructive lymphoid infiltration with intraepithelial lymphocytes in the superficial mucosa and in the glands.

Negative

Jejunum, duodenum,

mesenteric lymph nodes

6 years and

3 months

Resolved

[16]

6

53 years

MM

(1) Three cycles of VAD

(2) High-dose melphalan: Prednisolone and cyclosporin A for erythroderma

AITL

(Lymph node) Nodular infiltration of atypical lymphocytes with large nucleoli.

Positive

Brain, axillary and inguinal lymph nodes

10 months

Resolved

[17]

Our case

53 years

DLBCL

(1) Six cycle of R-CHOP

(2) Three cycles of R-ACES

PTCL-NOS

(Lung) Diffuse infiltration of small to medium-sized lymphocytes with multiple granulomas.

Positive

Supraclavicular, mediastinal, hilar, paraaortic, mesenteric lymph nodes, lungs

4 years

Fatal

 
  1. HL Hodgkin lymphoma, AITL angioimmunoblastic T-cell lymphoma, FL follicular lymphoma, DLBCL diffuse large B-cell lymphoma, MM multiple myeloma, PTCL-NOS peripheral T-cell lymphoma, not otherwise specified, T-LGL T-cell large granular lymphocytic leukemia, R-CHOP rituximab, cyclophosphamide, doxorubicin, and vincristine, MINE mesna, ifosfamide, mitoxantrone, and etoposide, ESHAP etoposide, cytarabine, cisplatin, and methylprednisolone, MCVAC ranimustine, cytarabine, etoposide, and cyclophosphamide, VAD vincristine, doxorubicin, and dexamethasone, CVP cyclophosphamide, prednisolone, and vincristine, AutoHASCT autologous hematopoietic stem cell transplantation, R-ACES rituximab, high-dose Ara C, carboplatin, etoposide, and steroids