Laky D, Rădulescu D
Victor Babes Institute, Surgery Department of the Cantacuzino Hospital, Bucharest, Romania.
Rom J Morphol Embryol. 1994 Jan-Jun;40(1-2):55-7.
The case of a 35-years-old patient with a progressive and densely developed subcutaneous tumour comprising the whole right cervical and subcutaneous region is presented. The tumour was painless of pale brown and light red colour, with no adherence on the epidermis and subjacent muscles. The patient has no pathological symptoms. After the histopathological examination we found the dermal infiltration with small, round or oval hyperchromatic cells and the histoenzymological investigation revealed intense positive markers CLA and MB2 pleading for their leukocytic nature while L26 reaction attested the B-cell nature of these lymphocytes and the diagnosis of polymorphous centroblastic malignant lymphoma (K type Working Classification).
本文报告了一例35岁患者,其右侧颈部及皮下区域出现一个进行性生长且致密的皮下肿瘤。该肿瘤无痛,呈浅棕色和浅红色,与表皮及下方肌肉无粘连。患者无病理症状。组织病理学检查发现真皮内有小的圆形或椭圆形深染细胞浸润,组织酶学研究显示CLA和MB2标记强烈阳性,提示其具有白细胞性质,而L26反应证实这些淋巴细胞为B细胞性质,诊断为多形性中心母细胞性恶性淋巴瘤(工作分类K型)。