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Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia
Lymphomatoid papulosis (LyP) is a chronic, recurrent benign skin disease characterized by histological features of a CD 30-positive cutaneous T-cell lymphoproliferative disorder. It is rare, with an annual, worldwide incidence of 1.2 - 1.9 per million, and accounts for 16-47% of pediatric cutaneous...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383590/ https://www.ncbi.nlm.nih.gov/pubmed/34434478 http://dx.doi.org/10.14740/jmc3718 |
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author | Oura, Kazumi Sato, Tomonobu Iguchi, Akihiro Toriumi, Naohisa Sarashina, Takeo |
author_facet | Oura, Kazumi Sato, Tomonobu Iguchi, Akihiro Toriumi, Naohisa Sarashina, Takeo |
author_sort | Oura, Kazumi |
collection | PubMed |
description | Lymphomatoid papulosis (LyP) is a chronic, recurrent benign skin disease characterized by histological features of a CD 30-positive cutaneous T-cell lymphoproliferative disorder. It is rare, with an annual, worldwide incidence of 1.2 - 1.9 per million, and accounts for 16-47% of pediatric cutaneous lymphoproliferative disorders. It often occurs on the extremities or the trunk and rarely affects the face or genitals. Its onset may be triggered by irradiation therapy, immunomodulating agents, infection or atopic dermatitis. It has a benign course but is associated with certain hematological malignancies. Mycosis fungoides and primary cutaneous anaplastic large cell lymphoma are the most commonly associated hematological malignancies. The incidence of lymphoma in children with LyP has been reported to be 8.5% at most. Most patients who develop lymphomas do so within 4 years of the LyP onset; therefore, patients with LyP should be carefully followed up. Herein, we report a case in which tumors appeared in the left scrotum and under the left lip during maintenance therapy for precursor B-cell acute lymphoblastic leukemia. We needed to distinguish the tumor from extramedullary recurrence of ALL or de novo other cutaneous lymphoma; however, the histological findings of a tumor biopsy resulted in a diagnosis of LyP. |
format | Online Article Text |
id | pubmed-8383590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-83835902021-08-24 Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia Oura, Kazumi Sato, Tomonobu Iguchi, Akihiro Toriumi, Naohisa Sarashina, Takeo J Med Cases Case Report Lymphomatoid papulosis (LyP) is a chronic, recurrent benign skin disease characterized by histological features of a CD 30-positive cutaneous T-cell lymphoproliferative disorder. It is rare, with an annual, worldwide incidence of 1.2 - 1.9 per million, and accounts for 16-47% of pediatric cutaneous lymphoproliferative disorders. It often occurs on the extremities or the trunk and rarely affects the face or genitals. Its onset may be triggered by irradiation therapy, immunomodulating agents, infection or atopic dermatitis. It has a benign course but is associated with certain hematological malignancies. Mycosis fungoides and primary cutaneous anaplastic large cell lymphoma are the most commonly associated hematological malignancies. The incidence of lymphoma in children with LyP has been reported to be 8.5% at most. Most patients who develop lymphomas do so within 4 years of the LyP onset; therefore, patients with LyP should be carefully followed up. Herein, we report a case in which tumors appeared in the left scrotum and under the left lip during maintenance therapy for precursor B-cell acute lymphoblastic leukemia. We needed to distinguish the tumor from extramedullary recurrence of ALL or de novo other cutaneous lymphoma; however, the histological findings of a tumor biopsy resulted in a diagnosis of LyP. Elmer Press 2021-08 2021-07-03 /pmc/articles/PMC8383590/ /pubmed/34434478 http://dx.doi.org/10.14740/jmc3718 Text en Copyright 2021, Oura et al. https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Oura, Kazumi Sato, Tomonobu Iguchi, Akihiro Toriumi, Naohisa Sarashina, Takeo Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia |
title | Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia |
title_full | Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia |
title_fullStr | Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia |
title_full_unstemmed | Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia |
title_short | Lymphomatoid Papulosis Development in Acute Lymphoblastic Leukemia |
title_sort | lymphomatoid papulosis development in acute lymphoblastic leukemia |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8383590/ https://www.ncbi.nlm.nih.gov/pubmed/34434478 http://dx.doi.org/10.14740/jmc3718 |
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