Breast implant-associated anaplastic large cell lymphoma: two distinct clinicopathological variants with different outcomes.
Abstract
[BACKGROUND] ALK-negative anaplastic large cell lymphoma associated with breast implant (i-ALCL) has been recently recognized as a distinct entity. Among 43 830 lymphomas registered in the French Lymphopath network since 2010, 300 breast lymphomas comprising 25 peripheral T-cell lymphomas (PTCL) were reviewed. Among PTCL, ALK-negative ALCL was the most frequent and all of them were associated with breast implants.
[PATIENTS AND METHODS] Since 2010, all i-ALCL cases were collected from different institutions through Lymphopath. Immuno-morphologic features, molecular data and clinical outcome of 19 i-ALCLs have been retrospectively analyzed.
[RESULTS] The median age of the patients was 61 years and the median length between breast implant and i-ALCL was 9 years. Most implants were silicone-filled and textured. Implant removal was performed in 17 out of 19 patients with additional treatment based on mostly CHOP or CHOP-like chemotherapy regimens (n = 10/19) or irradiation (n = 1/19). CHOP alone or ABVD following radiation without implant removal have been given in two patients. The two clinical presentations, i.e. effusion and less frequently tumor mass correlated with distinct histopathologic features: in situ i-ALCL (anaplastic cell proliferation confined to the fibrous capsule) and infiltrative i-ALCL (pleomorphic cells massively infiltrating adjacent tissue with eosinophils and sometimes Reed-Sternberg-like cells mimicking Hodgkin lymphoma). Malignant cells were CD30-positive, showed a variable staining for EMA and were ALK negative. Most cases had a cytotoxic T-cell immunophenotype with variable T-cell antigen loss and pSTAT3 nuclear expression. T-cell receptor genes were clonally rearranged in 13 out of 13 tested cases. After 18 months of median follow-up, the 2-year overall survival for in situ and infiltrative i-ALCL was 100% and 52.5%, respectively.
[CONCLUSIONS] In situ i-ALCLs have an indolent clinical course and generally remain free of disease after implant removal. However, infiltrative i-ALCLs could have a more aggressive clinical course that might require additional therapy to implant removal.
[PATIENTS AND METHODS] Since 2010, all i-ALCL cases were collected from different institutions through Lymphopath. Immuno-morphologic features, molecular data and clinical outcome of 19 i-ALCLs have been retrospectively analyzed.
[RESULTS] The median age of the patients was 61 years and the median length between breast implant and i-ALCL was 9 years. Most implants were silicone-filled and textured. Implant removal was performed in 17 out of 19 patients with additional treatment based on mostly CHOP or CHOP-like chemotherapy regimens (n = 10/19) or irradiation (n = 1/19). CHOP alone or ABVD following radiation without implant removal have been given in two patients. The two clinical presentations, i.e. effusion and less frequently tumor mass correlated with distinct histopathologic features: in situ i-ALCL (anaplastic cell proliferation confined to the fibrous capsule) and infiltrative i-ALCL (pleomorphic cells massively infiltrating adjacent tissue with eosinophils and sometimes Reed-Sternberg-like cells mimicking Hodgkin lymphoma). Malignant cells were CD30-positive, showed a variable staining for EMA and were ALK negative. Most cases had a cytotoxic T-cell immunophenotype with variable T-cell antigen loss and pSTAT3 nuclear expression. T-cell receptor genes were clonally rearranged in 13 out of 13 tested cases. After 18 months of median follow-up, the 2-year overall survival for in situ and infiltrative i-ALCL was 100% and 52.5%, respectively.
[CONCLUSIONS] In situ i-ALCLs have an indolent clinical course and generally remain free of disease after implant removal. However, infiltrative i-ALCLs could have a more aggressive clinical course that might require additional therapy to implant removal.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 해부 | breast
|
유방 | dict | 5 | |
| 합병증 | anaplastic large cell lymphoma
|
보형물연관 역형성대세포림프종 | dict | 2 | |
| 해부 | anaplastic cell
|
scispacy | 1 | ||
| 해부 | tissue
|
scispacy | 1 | ||
| 해부 | eosinophils
|
scispacy | 1 | ||
| 해부 | Reed-Sternberg-like cells
|
scispacy | 1 | ||
| 해부 | Malignant cells
|
scispacy | 1 | ||
| 약물 | CHOP-like
|
scispacy | 1 | ||
| 약물 | ABVD
|
C0050380
bleomycin/dacarbazine/doxorubicin/vinblastine protocol
|
scispacy | 1 | |
| 약물 | T-cell antigen loss
|
scispacy | 1 | ||
| 약물 | [BACKGROUND] ALK-negative anaplastic large cell lymphoma
|
scispacy | 1 | ||
| 약물 | CHOP
|
scispacy | 1 | ||
| 약물 | [CONCLUSIONS] In
|
scispacy | 1 | ||
| 질환 | Breast implant-associated anaplastic large cell lymphoma
|
C4528210
Breast implant-associated anaplastic large-cell lymphoma
|
scispacy | 1 | |
| 질환 | ALK-negative anaplastic
|
scispacy | 1 | ||
| 질환 | breast implant
|
C0178391
breast implant procedure
|
scispacy | 1 | |
| 질환 | lymphomas
|
C0024299
Lymphoma
|
scispacy | 1 | |
| 질환 | breast lymphomas
|
C1704251
Breast Lymphoma
|
scispacy | 1 | |
| 질환 | peripheral T-cell lymphomas
|
C0079774
Peripheral T-Cell Lymphoma
|
scispacy | 1 | |
| 질환 | PTCL
→ peripheral T-cell lymphomas
|
C0079774
Peripheral T-Cell Lymphoma
|
scispacy | 1 | |
| 질환 | ALK-negative ALCL
|
scispacy | 1 | ||
| 질환 | effusion
|
C0013687
effusion
|
scispacy | 1 | |
| 질환 | tumor
|
C0027651
Neoplasms
|
scispacy | 1 | |
| 질환 | anaplastic
|
C0205618
Undifferentiated
|
scispacy | 1 | |
| 질환 | fibrous
|
C0439709
Fibrous
|
scispacy | 1 | |
| 질환 | Hodgkin lymphoma
|
C0019829
Hodgkin Disease
|
scispacy | 1 | |
| 질환 | CD30-positive
|
scispacy | 1 | ||
| 질환 | fibrous capsule
|
scispacy | 1 | ||
| 질환 | infiltrative i-ALCL (pleomorphic cells
|
scispacy | 1 | ||
| 기타 | patients
|
scispacy | 1 | ||
| 기타 | EMA
|
scispacy | 1 | ||
| 기타 | ALK
|
scispacy | 1 | ||
| 기타 | T-cell antigen
|
scispacy | 1 | ||
| 기타 | pSTAT3 nuclear
|
scispacy | 1 | ||
| 기타 | T-cell receptor
|
scispacy | 1 |
MeSH Terms
Adult; Aged; Aged, 80 and over; Anaplastic Lymphoma Kinase; Breast Implants; Female; Hodgkin Disease; Humans; Immunophenotyping; Ki-1 Antigen; Lymphoma, Large-Cell, Anaplastic; Lymphoma, T-Cell, Peripheral; Middle Aged; Receptor Protein-Tyrosine Kinases; Receptors, Antigen, T-Cell; Retrospective Studies; STAT3 Transcription Factor; Silicones; T-Lymphocytes, Cytotoxic
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