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Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report
Patient: Female, 51 Final Diagnosis: Breast implant associated anaplastic large cell lymphoma Symptoms: Breast swelling Medication: — Clinical Procedure: Surgery Specialty: Oncology OBJECTIVE: Rare disease BACKGROUND: Anaplastic large cell lymphomas (ALCL) are a rare type of primary breast lymphoma....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460956/ https://www.ncbi.nlm.nih.gov/pubmed/28559535 http://dx.doi.org/10.12659/AJCR.903161 |
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author | Evren, Sevan Khoury, Thaer Neppalli, Vishalla Cappuccino, Helen Hernandez-Ilizaliturri, Francisco J. Kumar, Prasanna |
author_facet | Evren, Sevan Khoury, Thaer Neppalli, Vishalla Cappuccino, Helen Hernandez-Ilizaliturri, Francisco J. Kumar, Prasanna |
author_sort | Evren, Sevan |
collection | PubMed |
description | Patient: Female, 51 Final Diagnosis: Breast implant associated anaplastic large cell lymphoma Symptoms: Breast swelling Medication: — Clinical Procedure: Surgery Specialty: Oncology OBJECTIVE: Rare disease BACKGROUND: Anaplastic large cell lymphomas (ALCL) are a rare type of primary breast lymphoma. The association between breast implants and ALCL was first described in 1997 and since then 34–173 cases have been presented. The annual incidence of breast implant-associated ALCL (BI-ALCL) is 0.1–0.3 per 100 000 women who undergo breast reconstruction, and cases are often underreported due to the rarity of these tumors. BI-ALCL arises from the inflammatory T cells surrounding the fibrous capsule, and most tumors are in situ. CASE REPORT: Here, we present the case of a 51-year-old woman with ALCL following bilateral silicone breast implants. The patient presented with breast enlargement and tenderness 9 years following reconstructive surgery. Imagining studies showed fluid collection surrounding the affected breast implant. Staging studies and histocytopathology examination confirmed the presence BI-ALCL without capsular invasion or metastasis. Complete surgical excision was performed. The patient continues to be in complete remission. CONCLUSIONS: Due to the rarity of these tumors, establishing the diagnosis of BI-ALCL can be challenging and requires a multidisciplinary approach. Clinicians should be aware of the relationship between breast implants and BI-ALCL. |
format | Online Article Text |
id | pubmed-5460956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54609562017-06-14 Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report Evren, Sevan Khoury, Thaer Neppalli, Vishalla Cappuccino, Helen Hernandez-Ilizaliturri, Francisco J. Kumar, Prasanna Am J Case Rep Articles Patient: Female, 51 Final Diagnosis: Breast implant associated anaplastic large cell lymphoma Symptoms: Breast swelling Medication: — Clinical Procedure: Surgery Specialty: Oncology OBJECTIVE: Rare disease BACKGROUND: Anaplastic large cell lymphomas (ALCL) are a rare type of primary breast lymphoma. The association between breast implants and ALCL was first described in 1997 and since then 34–173 cases have been presented. The annual incidence of breast implant-associated ALCL (BI-ALCL) is 0.1–0.3 per 100 000 women who undergo breast reconstruction, and cases are often underreported due to the rarity of these tumors. BI-ALCL arises from the inflammatory T cells surrounding the fibrous capsule, and most tumors are in situ. CASE REPORT: Here, we present the case of a 51-year-old woman with ALCL following bilateral silicone breast implants. The patient presented with breast enlargement and tenderness 9 years following reconstructive surgery. Imagining studies showed fluid collection surrounding the affected breast implant. Staging studies and histocytopathology examination confirmed the presence BI-ALCL without capsular invasion or metastasis. Complete surgical excision was performed. The patient continues to be in complete remission. CONCLUSIONS: Due to the rarity of these tumors, establishing the diagnosis of BI-ALCL can be challenging and requires a multidisciplinary approach. Clinicians should be aware of the relationship between breast implants and BI-ALCL. International Scientific Literature, Inc. 2017-05-31 /pmc/articles/PMC5460956/ /pubmed/28559535 http://dx.doi.org/10.12659/AJCR.903161 Text en © Am J Case Rep, 2017 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Articles Evren, Sevan Khoury, Thaer Neppalli, Vishalla Cappuccino, Helen Hernandez-Ilizaliturri, Francisco J. Kumar, Prasanna Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report |
title | Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report |
title_full | Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report |
title_fullStr | Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report |
title_full_unstemmed | Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report |
title_short | Breast Implant-Associated Anaplastic Large Cell Lymphoma (ALCL): A Case Report |
title_sort | breast implant-associated anaplastic large cell lymphoma (alcl): a case report |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5460956/ https://www.ncbi.nlm.nih.gov/pubmed/28559535 http://dx.doi.org/10.12659/AJCR.903161 |
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