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Correspondence

γ/δ T-Cell Lymphoma of the Thyroid Gland

N Engl J Med 1997; 336:1391-1392May 8, 1997

Article

To the Editor:

Lymphomas of the thyroid are almost exclusively of B-cell origin.1 We report a case of thyroid lymphoma with a γ/δ T-cell phenotype.

A 59-year-old Japanese woman was seen because of marked goiter. Chronic thyroiditis had been diagnosed one year before admission. Neither peripheral lymphadenopathy nor a rash was detected. Laboratory values were normal except for an elevated serum level of thyroglobulin. Serum antibodies against human T-cell lymphotropic virus type I and human immunodeficiency virus were not found. A few small bilateral lymph nodes were detected deep in the cervical region. Open biopsy of the thyroid tumor revealed diffuse replacement by atypical large lymphoid cells (Figure 1AFigure 1Histologic Findings in a Patient with a Thyroid Tumor. and Figure 1B). Reactive lymphoid follicles with hypocellular germinal centers were found in and around the neoplastic area. The phenotype of lymphoma cells was CD3+CD4-CD8-CD19-CD20-CD56-. These cells reacted with a monoclonal antibody against T-cell receptor δ but not with a monoclonal antibody against T-cell receptor β. DNA analysis of the thyroid mass revealed a clonal rearrangement of the T-cell receptor δ-chain gene.

The patient was given a diagnosis of γ/δ T-cell lymphoma (clinical stage IIA) and was treated with five courses of combination therapy with cyclophosphamide, doxorubicin, vincristine, and prednisone and three courses of therapy with carboplatin, etoposide, ifosfamide, and dexamethasone, followed by 40 Gy of local irradiation. The size of the goiter was reduced by half, and no uptake of gallium was detected on scanning. Twenty-two months after diagnosis, the patient remains well, with no evidence of recurrence.

Thyroid B-cell lymphomas occur predominantly in elderly women. They are associated with chronic thyroiditis and have a relatively good prognosis.1,2 This type of lymphoma is thought to be a mucosa-associated lymphoma derived from lymphoid tissue.2 In our patient, the clinical and histopathological features closely resembled those of the usual thyroid B-cell lymphoma.

Peripheral γ/δ T-cell lymphoma has been reported in a limited number of anatomical sites, such as hepatosplenic, cutaneous, and nasopharyngeal regions.3,4 Our patient did not present with any of these features, but with diffuse enlargement of the thyroid gland. Although “hepatosplenic γ/δ T-cell lymphoma” is included as a provisional entity in a recently proposed revised European–American classification of lymphoid neoplasms5 and is well recognized, not all the characteristics of γ/δ T-cell lymphoma are known. Our case report demonstrates that γ/δ T-cell lymphomas can involve unusual extranodal sites.

Motoko Yamaguchi, M.D.
Toshiyuki Ohno, M.D., Ph.D.
Kenkichi Kita, M.D., Ph.D.
Mie University School of Medicine, Tsu 514, Japan

5 References
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    Noriko Motoi, Yasunori Ozawa. (2005) Malignant T-cell lymphoma of the thyroid gland associated with Hashimoto's thyroiditis. Pathology International 55:7, 425-430
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    Mariano P. Scolnik, Rubn A. Burgos, Anala Paz, Mariela Weinreiter, Mara del Carmen Ardaiz, Patricia Bare, Mara Carolina Bayo Hanza, Marcela A. de Dios Soler, Marina Ins Narbaitz, Mara Fernanda Palacios, Adhelma Sasot, Ana Huberman, Mara Marta de E de Bracco. (2000) Nonhepatosplenic ?? T-cell lymphoma with initial testicular compromise. American Journal of Hematology 65:3, 260-262
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    Gregory A. Derringer, Lester D. R. Thompson, R. Allen Frommelt, Karen E. Bijwaard, Clara S. Heffess, Susan L. Abbondanzo. (2000) Malignant Lymphoma of the Thyroid Gland. The American Journal of Surgical Pathology 24:5, 623-639
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