[Lymphoma and other rare malignant tumors of the thyroid].

UNLABELLED Primary thyroid lymphomas are rare. Surgery is seldom indicated. The aim of the study is to find out the main characteristics of primary thyroid lymphomas in our patients, indications for surgery and the possibility of treatment. frequency and characteristics of rare thyroid tumors. METHOD Retrospective study of 1044 patient operated for malignant thyroid tumor. RESULTS From 1995 to may 2003. We operated upon 15 patients with primary thyroid lymphomas. 2 men and 13 women mean age of 50.12 years (from 22 to 74 years), also one patient of age 69 with insular thyroid cancer. Reason for surgery was thyroid tumor in all, compressive disturbances in 9, among them 4 with asphyxia. Radical total thyroidectomy was performed in 4 (26.7%), whole in others some residual tumor tissue was could not be removed in spite of thyroidectomy in 3, hemithyroidectomy in 2, tumor debulking in 5 and only open biopsy was performed in one patient. There was no operative mortality. no postoperative hypocalcaemia and no recurrent nerve palsy. Histological type of tumor was Non-Hodgkin lymphoma in 13 patients, Hodgkin disease in 2 female patients of age 22 and 24. Hashimoto thyroiditis was present in 3 patients. After surgery, 13 patients were treated with chemotherapy, one patient died one month after the operation and one patient refused chemotherapy. Follow-up data are available for 9 patients and the mean follow-up period was 20 months (1-48 months). Three patients died after a month, 2 and 3 years after surgery. Six patients are without local relapse. In one patient who refused chemotherapy, a year after thyroid surgery, resection of large intestine was performed because of lymphoma of the colon. CONCLUSION Malignant thyroid lymphomas are rare. They present with rapidly growing thyroid tumor, compression and asphyxia. Surgery is only temporarily effective and it is necessary to start with chemo-radiotherapy as soon as possible. Rare forms of thyroid cancer have to be histologically recognised in order to choose the best way of treatment.

[1]  E. Bergstralh,et al.  Non-Hodgkin's lymphoma of the thyroid: Is more than biopsy necessary? , 1992, World Journal of Surgery.

[2]  A. Belfiore,et al.  Long‐term outcome of patients with insular carcinoma of the thyroid , 2002, Cancer.

[3]  J. Leroy,et al.  Hodgkin's disease masquerading as fibrous thyroiditis: potential role of cytokines in in vivo and in vitro studies , 2002, Clinical endocrinology.

[4]  H. Schultz,et al.  Primary Thyroid Lymphoma: A Retrospective Analysis of Prognostic Factors and Treatment Outcome for Localized Intermediate and High Grade Lymphoma , 2001, American journal of clinical oncology.

[5]  T. Loree,et al.  Clinical Presentation and Treatment of Non-Hodgkin’s Lymphoma of the Thyroid Gland , 2001, Annals of Surgical Oncology.

[6]  P. Parrilla,et al.  Insular carcinoma: an infrequent subtype of thyroid cancer. , 1998, Journal of the American College of Surgeons.

[7]  M. Dharan,et al.  Hodgkin's Disease Presenting as a Solitary Thyroid Nodule , 1995, Clinical nuclear medicine.

[8]  I. Narabayashi,et al.  Clinical aspects of primary thyroid lymphoma: diagnosis and treatment based on our experience of 119 cases. , 1993, Thyroid : official journal of the American Thyroid Association.

[9]  D. Fermont,et al.  Non-Hodgkin's lymphoma of the thyroid. , 1987, Clinical radiology.

[10]  J. Rosai,et al.  Poorly differentiated (“insular”) thyroid carcinoma: A reinterpretation of Langhans' “wuchernde Struma” , 1984, The American journal of surgical pathology.