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09 March 2025 : Case report  Japan

A 58-Year-Old Man with a History of Autoimmune Thyroiditis Diagnosed with Mucosa-Associated Lymphoid Tissue Lymphoma and Papillary Carcinoma of the Thyroid

Challenging differential diagnosis, Rare disease

Naru Babaya ORCID logo ABCDEF 1*, Sawa Yoshida ORCID logo ABCD 1, Shinsuke Noso ORCID logo D 1, Yoshihisa Hiromine ORCID logo D 1, Yasunori Taketomo ORCID logo D 1, Takayuki Kimura BD 2, Hiroaki Kakutani BD 3, Takao Satou BD 4, Hiroshi Ikegami ORCID logo DE 1, Norikazu Maeda ORCID logo DE 1

DOI: 10.12659/AJCR.946022

Am J Case Rep 2025; 26:e946022

Figure 4. Photomicrographs of the histopathology of mucosa-assisted lymphoid tissue (MALT) lymphoma of the thyroid gland. (A) Hematoxylin and eosin staining (×400). A substantial portion of normal thyroid architecture appears to be replaced by dense, diffuse infiltrates of small, atypical lymphocytes. (B) Immunohistochemical labeling for IRTA1 (×600). Diffusely proliferated small lymphocytes are IRTA1 positive. (C, D) Immunohistochemical labeling for immunoglobulin light chain, kappa (C), and lambda (D) (×600). The ratio of κ-positive cells to λ-positive cells is more than 10-fold, considered an obvious light chain restriction, and can be judged as monoclonal B-cell proliferation. Scale bar: 50 μm.

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923