Chakraborty Jayati, Paul Prabir Chandra, Sarkar Ranu, Rao R Nagarjun
Department of Pathology, Bankura Sammilani Medical College, Bankura.
Indian J Pathol Microbiol. 2007 Apr;50(2):315-7.
Primary breast lymphoma is a relatively uncommon neoplasm, majority being of B-cell origin. Mucosa associated lymphoid tissue (MALT) is one of the common types of breast lymphomas. Though cytologic diagnosis of breast lymphoma is an easy procedure and provides guidance for appropriate pre-operative management, it is often impossible to differentiate a low grade lymphoma from reactive proliferation. A similar difficulty was encountered in the present case, a 42 year old female with a breast lump. Fine needle aspiration cytology revealed a mixed lymphoid cell population. Lymphoepithelial lesions were identified histologically, and the majority of the cell population were confirmed as lymphoma cells of B-cell origin on immunohistochemistry. This case highlights the limitations of cytology and the importance of histological examination supported by immunohistochemistry for making a diagnosis of low grade primary breast lymphoma.
原发性乳腺淋巴瘤是一种相对罕见的肿瘤,大多数起源于B细胞。黏膜相关淋巴组织(MALT)淋巴瘤是乳腺淋巴瘤的常见类型之一。虽然乳腺淋巴瘤的细胞学诊断是一个简单的程序,并可为适当的术前管理提供指导,但通常无法将低级别淋巴瘤与反应性增生区分开来。本病例为一名42岁有乳腺肿块的女性,也遇到了类似的困难。细针穿刺细胞学检查显示为混合性淋巴细胞群。组织学上发现了淋巴上皮病变,免疫组化证实大多数细胞群为B细胞起源的淋巴瘤细胞。该病例突出了细胞学的局限性以及免疫组化支持下的组织学检查对诊断低级别原发性乳腺淋巴瘤的重要性。