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Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin

BACKGROUND: Cutaneous B-cell lymphomas represent about 25% of all cutaneous lymphomas. Peripheral diffuse large B-cell lymphoma of the leg type is the most aggressive subtype seen mainly in elderly patients. Treatment is not standardised. CASE REPORT: An 87-year-old female patient was presented in M...

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Autores principales: Wollina, Uwe, Schmidt, Nadine, Schönlebe, Jacqueline, Vojvodic, Aleksandra, Hansel, Gesina, Koch, André, Lotti, Torello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Republic of Macedonia 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910811/
https://www.ncbi.nlm.nih.gov/pubmed/31850110
http://dx.doi.org/10.3889/oamjms.2019.565
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author Wollina, Uwe
Schmidt, Nadine
Schönlebe, Jacqueline
Vojvodic, Aleksandra
Hansel, Gesina
Koch, André
Lotti, Torello
author_facet Wollina, Uwe
Schmidt, Nadine
Schönlebe, Jacqueline
Vojvodic, Aleksandra
Hansel, Gesina
Koch, André
Lotti, Torello
author_sort Wollina, Uwe
collection PubMed
description BACKGROUND: Cutaneous B-cell lymphomas represent about 25% of all cutaneous lymphomas. Peripheral diffuse large B-cell lymphoma of the leg type is the most aggressive subtype seen mainly in elderly patients. Treatment is not standardised. CASE REPORT: An 87-year-old female patient was presented in May 2018 because of the development of painless subcutaneous nodules on the legs since late 2017. On examination, we observed up to 5 cm large erythematous nodules on the legs and a smaller plaque in the left submammary fold. The histology of a skin demonstrated tumour infiltrate that was separated from the overlying epidermis by a grenz zone. It consisted of densely packed, blastoid lymphocytic cells with numerous, and some atypical mitoses. The cells were positive for CD20, CD79A and CD5. Almost 100% of the cells were labelled with Ki67. The diagnosis of a diffuse large B-cell lymphoma (PCLBCL-LT) of the leg was confirmed. Histologic analysis of a bone marrow biopsy demonstrated a hypercellular bone marrow without malignant lymphatic infiltrates. Diagnostic ultrasound of cervical nodes and computerised tomography (CT) scans (native and with contrast medium) of head, neck and trunk excluded an extracutaneous manifestation of the PCLBCL-LT. Treatment with rituximab plus bendamustibe was initiated, but tumour progress was noted after the second course. Suggested palliative therapy with radiation and rituximab was refused. The patient died 7 months after diagnosis. CONCLUSIONS: Although some trials suggested a beneficial effect of immuno-chemotherapy, the prognosis of (PCLBCL-LT) remains poor. Standardised treatment is missing due to the relative rarity of this malignancy.
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spelling pubmed-69108112019-12-17 Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin Wollina, Uwe Schmidt, Nadine Schönlebe, Jacqueline Vojvodic, Aleksandra Hansel, Gesina Koch, André Lotti, Torello Open Access Maced J Med Sci Case Report BACKGROUND: Cutaneous B-cell lymphomas represent about 25% of all cutaneous lymphomas. Peripheral diffuse large B-cell lymphoma of the leg type is the most aggressive subtype seen mainly in elderly patients. Treatment is not standardised. CASE REPORT: An 87-year-old female patient was presented in May 2018 because of the development of painless subcutaneous nodules on the legs since late 2017. On examination, we observed up to 5 cm large erythematous nodules on the legs and a smaller plaque in the left submammary fold. The histology of a skin demonstrated tumour infiltrate that was separated from the overlying epidermis by a grenz zone. It consisted of densely packed, blastoid lymphocytic cells with numerous, and some atypical mitoses. The cells were positive for CD20, CD79A and CD5. Almost 100% of the cells were labelled with Ki67. The diagnosis of a diffuse large B-cell lymphoma (PCLBCL-LT) of the leg was confirmed. Histologic analysis of a bone marrow biopsy demonstrated a hypercellular bone marrow without malignant lymphatic infiltrates. Diagnostic ultrasound of cervical nodes and computerised tomography (CT) scans (native and with contrast medium) of head, neck and trunk excluded an extracutaneous manifestation of the PCLBCL-LT. Treatment with rituximab plus bendamustibe was initiated, but tumour progress was noted after the second course. Suggested palliative therapy with radiation and rituximab was refused. The patient died 7 months after diagnosis. CONCLUSIONS: Although some trials suggested a beneficial effect of immuno-chemotherapy, the prognosis of (PCLBCL-LT) remains poor. Standardised treatment is missing due to the relative rarity of this malignancy. Republic of Macedonia 2019-06-30 /pmc/articles/PMC6910811/ /pubmed/31850110 http://dx.doi.org/10.3889/oamjms.2019.565 Text en Copyright: © 2019 Uwe Wollina, Nadine Schmidt, Jacqueline Schönlebe, Aleksandra Vojvodic, Gesina Hansel, André Koch, Torello Lotti. http://creativecommons.org/licenses/CC BY-NC/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0)
spellingShingle Case Report
Wollina, Uwe
Schmidt, Nadine
Schönlebe, Jacqueline
Vojvodic, Aleksandra
Hansel, Gesina
Koch, André
Lotti, Torello
Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin
title Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin
title_full Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin
title_fullStr Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin
title_full_unstemmed Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin
title_short Large B - Cell Lymphoma of the Leg – Unfavourable Course with Rituximab/Bendamustin
title_sort large b - cell lymphoma of the leg – unfavourable course with rituximab/bendamustin
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6910811/
https://www.ncbi.nlm.nih.gov/pubmed/31850110
http://dx.doi.org/10.3889/oamjms.2019.565
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