Mantle Cell Lymphoma in the Thyroid: A Rare Presentation

Background. While 2% of all extranodal Non-Hodgkin Lymphomas present in the thyroid, there exists insufficient data to describe the incidence of mantle cell lymphoma in the thyroid. A case series of 1400 patients revealed that <1% of thyroid lymphomas may be MCL; hence better understanding of the...

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Main Authors: Uzma Mohammad Siddiqui, Sarika N. Rao, Pallavi Kanwar Galera, Nahida Islam, Mira S. Torres
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Case Reports in Pathology
Online Access:http://dx.doi.org/10.1155/2017/6749801
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author Uzma Mohammad Siddiqui
Sarika N. Rao
Pallavi Kanwar Galera
Nahida Islam
Mira S. Torres
author_facet Uzma Mohammad Siddiqui
Sarika N. Rao
Pallavi Kanwar Galera
Nahida Islam
Mira S. Torres
author_sort Uzma Mohammad Siddiqui
collection DOAJ
description Background. While 2% of all extranodal Non-Hodgkin Lymphomas present in the thyroid, there exists insufficient data to describe the incidence of mantle cell lymphoma in the thyroid. A case series of 1400 patients revealed that <1% of thyroid lymphomas may be MCL; hence better understanding of the disease course is essential. Patient Findings. A 65-year-old female was referred for a multinodular goiter. Multiple fine needle aspirations from the dominant right nodule were consistent with Hashimoto’s thyroiditis and flow cytometry was negative. Due to progressing dysphagia, she underwent total thyroidectomy. Summary. Pathology revealed MCL with mantle zone growth pattern in the right thyroid. Flow cytometry showed monoclonal B cells comprising 9% of total cells. The Ki-67 index was 10%. She was diagnosed as having stage IIE MCL and offered conservative management by medical oncology, given that she had no B symptoms. Conclusion. Though chemotherapy is the treatment of choice in MCL, a subset of patients with low-grade disease may be observed. As in our patient, mantle zone growth pattern and a Ki-67 index < 10% suggest a favorable prognosis. A diagnosis of primary MCL in the thyroid remains rare and staging modalities as well as treatment options continue to evolve.
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spelling doaj-art-a845af9c57f3472ba1cc9e23416d58422025-02-03T00:59:19ZengWileyCase Reports in Pathology2090-67812090-679X2017-01-01201710.1155/2017/67498016749801Mantle Cell Lymphoma in the Thyroid: A Rare PresentationUzma Mohammad Siddiqui0Sarika N. Rao1Pallavi Kanwar Galera2Nahida Islam3Mira S. Torres4Division of Endocrinology, University of Massachusetts Medical School, 55 Lake Avenue N., Worcester, MA 01655, USASection of Endocrinology, MedStar Washington Hospital Center, 110 Irving St NW, Suite 2A-72, Washington, DC 20010, USADepartment of Pathology, University of Massachusetts Medical School, Biotech 3, 1 Innovation Drive, Worcester, MA, USADivision of Hematology and Oncology, University of Massachusetts Medical School, 55 Lake Avenue N., Worcester, MA 01655, USADivision of Endocrinology, University of Massachusetts Medical School, 55 Lake Avenue N., Worcester, MA 01655, USABackground. While 2% of all extranodal Non-Hodgkin Lymphomas present in the thyroid, there exists insufficient data to describe the incidence of mantle cell lymphoma in the thyroid. A case series of 1400 patients revealed that <1% of thyroid lymphomas may be MCL; hence better understanding of the disease course is essential. Patient Findings. A 65-year-old female was referred for a multinodular goiter. Multiple fine needle aspirations from the dominant right nodule were consistent with Hashimoto’s thyroiditis and flow cytometry was negative. Due to progressing dysphagia, she underwent total thyroidectomy. Summary. Pathology revealed MCL with mantle zone growth pattern in the right thyroid. Flow cytometry showed monoclonal B cells comprising 9% of total cells. The Ki-67 index was 10%. She was diagnosed as having stage IIE MCL and offered conservative management by medical oncology, given that she had no B symptoms. Conclusion. Though chemotherapy is the treatment of choice in MCL, a subset of patients with low-grade disease may be observed. As in our patient, mantle zone growth pattern and a Ki-67 index < 10% suggest a favorable prognosis. A diagnosis of primary MCL in the thyroid remains rare and staging modalities as well as treatment options continue to evolve.http://dx.doi.org/10.1155/2017/6749801
spellingShingle Uzma Mohammad Siddiqui
Sarika N. Rao
Pallavi Kanwar Galera
Nahida Islam
Mira S. Torres
Mantle Cell Lymphoma in the Thyroid: A Rare Presentation
Case Reports in Pathology
title Mantle Cell Lymphoma in the Thyroid: A Rare Presentation
title_full Mantle Cell Lymphoma in the Thyroid: A Rare Presentation
title_fullStr Mantle Cell Lymphoma in the Thyroid: A Rare Presentation
title_full_unstemmed Mantle Cell Lymphoma in the Thyroid: A Rare Presentation
title_short Mantle Cell Lymphoma in the Thyroid: A Rare Presentation
title_sort mantle cell lymphoma in the thyroid a rare presentation
url http://dx.doi.org/10.1155/2017/6749801
work_keys_str_mv AT uzmamohammadsiddiqui mantlecelllymphomainthethyroidararepresentation
AT sarikanrao mantlecelllymphomainthethyroidararepresentation
AT pallavikanwargalera mantlecelllymphomainthethyroidararepresentation
AT nahidaislam mantlecelllymphomainthethyroidararepresentation
AT mirastorres mantlecelllymphomainthethyroidararepresentation