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Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls

Breast involvement by lymphoma is uncommon and poses challenges in diagnosis. Lymphomas may clinically, radiologically, and morphologically mimic both benign and neoplastic conditions. We describe two cases of lymphoid malignancies predominantly involving the breast, both presenting diagnostic dilem...

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Autores principales: Farkash, Evan A., Ferry, Judith A., Harris, Nancy Lee, Hochberg, Ephraim P., Takvorian, Ronald W., Zuckerman, Dan S., Sohani, Aliyah R.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2798933/
https://www.ncbi.nlm.nih.gov/pubmed/20309431
http://dx.doi.org/10.1007/s12308-009-0043-y
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author Farkash, Evan A.
Ferry, Judith A.
Harris, Nancy Lee
Hochberg, Ephraim P.
Takvorian, Ronald W.
Zuckerman, Dan S.
Sohani, Aliyah R.
author_facet Farkash, Evan A.
Ferry, Judith A.
Harris, Nancy Lee
Hochberg, Ephraim P.
Takvorian, Ronald W.
Zuckerman, Dan S.
Sohani, Aliyah R.
author_sort Farkash, Evan A.
collection PubMed
description Breast involvement by lymphoma is uncommon and poses challenges in diagnosis. Lymphomas may clinically, radiologically, and morphologically mimic both benign and neoplastic conditions. We describe two cases of lymphoid malignancies predominantly involving the breast, both presenting diagnostic dilemmas. The first case, ALK-negative anaplastic large-cell lymphoma involving a seroma associated with a breast implant, is an emerging clinicopathologic entity. Anaplastic large-cell lymphoma has been identified in association with breast implants and seroma formation relatively recently. The second case, hairy cell leukemia involving the breast and ipsilateral axillary sentinel lymph node, is, to our knowledge, the first reported case of hairy cell leukemia involving the breast at the time of diagnosis. While a localized bone lesion was present at time of diagnosis, bone marrow involvement was relatively mild in comparison to that seen in the breast and lymph node. In the first case, lymphoma occurred in a clinical setting where malignancy was unsuspected, highlighting the importance of careful morphologic evaluation of paucicellular samples, as well as awareness of rare clinicopathologic entities, in avoiding a misdiagnosis of a benign inflammatory infiltrate. In the second case, the lymphoid neoplasm exhibited classic morphologic and immunophenotypic features, but presented at an unusual site of involvement. Knowledge of the patient's concurrent diagnosis of hairy cell leukemia involving the bone marrow and bone helped avoid a misdiagnosis of carcinoma rather than lymphoma.
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spelling pubmed-27989332009-12-30 Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls Farkash, Evan A. Ferry, Judith A. Harris, Nancy Lee Hochberg, Ephraim P. Takvorian, Ronald W. Zuckerman, Dan S. Sohani, Aliyah R. J Hematop Case Report Breast involvement by lymphoma is uncommon and poses challenges in diagnosis. Lymphomas may clinically, radiologically, and morphologically mimic both benign and neoplastic conditions. We describe two cases of lymphoid malignancies predominantly involving the breast, both presenting diagnostic dilemmas. The first case, ALK-negative anaplastic large-cell lymphoma involving a seroma associated with a breast implant, is an emerging clinicopathologic entity. Anaplastic large-cell lymphoma has been identified in association with breast implants and seroma formation relatively recently. The second case, hairy cell leukemia involving the breast and ipsilateral axillary sentinel lymph node, is, to our knowledge, the first reported case of hairy cell leukemia involving the breast at the time of diagnosis. While a localized bone lesion was present at time of diagnosis, bone marrow involvement was relatively mild in comparison to that seen in the breast and lymph node. In the first case, lymphoma occurred in a clinical setting where malignancy was unsuspected, highlighting the importance of careful morphologic evaluation of paucicellular samples, as well as awareness of rare clinicopathologic entities, in avoiding a misdiagnosis of a benign inflammatory infiltrate. In the second case, the lymphoid neoplasm exhibited classic morphologic and immunophenotypic features, but presented at an unusual site of involvement. Knowledge of the patient's concurrent diagnosis of hairy cell leukemia involving the bone marrow and bone helped avoid a misdiagnosis of carcinoma rather than lymphoma. Springer-Verlag 2009-08-20 /pmc/articles/PMC2798933/ /pubmed/20309431 http://dx.doi.org/10.1007/s12308-009-0043-y Text en © Springer-Verlag 2009
spellingShingle Case Report
Farkash, Evan A.
Ferry, Judith A.
Harris, Nancy Lee
Hochberg, Ephraim P.
Takvorian, Ronald W.
Zuckerman, Dan S.
Sohani, Aliyah R.
Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
title Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
title_full Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
title_fullStr Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
title_full_unstemmed Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
title_short Rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
title_sort rare lymphoid malignancies of the breast: a report of two cases illustrating potential diagnostic pitfalls
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2798933/
https://www.ncbi.nlm.nih.gov/pubmed/20309431
http://dx.doi.org/10.1007/s12308-009-0043-y
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