A case of Hodgkin's disease and non-Hodgkin lymphomas, occurred in different anatomical sites at simultaneous onset.

A. Masunaga, M. Matsuda, H. Hashimoto, M. Narabayashi, K. Maeda, Y. Imai, H. Ikeda, T. Shindo, Katsurou Takahashi
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Abstract

Discordant malignant lyphoma composed of Hodgkin's disease (HD) and non-Hodgkin lymphoma (NHD) which occurred in a 38 years-old Japanese male is reported. He suffered from slight fever (38°C), general fatigue since December 25 in 1985. Thereafter, axiller and inguinal lymph nodes swelling was noticed. Because of systemic lymph node swelling with anemia, he was hospitalized in Nagai City Hospital 2 weeks later. Cervical, axillar and inguinal lymph nodes were excised. He was received chemotherapy (Adr, End. Prd. L-Asp). 6 months after, he was transfered to Yamagata Prefectural Central Hospital. In spite of chemotherapy, he died of a clinically suspicious perforation of alimentary tract in January 1986. Autopsy was not permitted. Resected cervical and inguinal nodes revealed scattered mononucleated Hodgkin's (H) cells and multinucleated Reed-Sternberg (RS) cells with intermingled lymphocytes, eosinophils and plasma cells, so they were diagnosed as HD, mixed cellularity (MC) type. Axillar node showed a diffuse proliferation of small and large mononucleated cells with prominent nucleoli, without diagnostic H cells and/or RS cells, and diagnosed as NHL, diffuse, mixed. Immunohistochemically, some of H cells and RS cells in cervical and inguinal nodes were positive for B1, MB1 and polyclonal cIgs (IgG, A, κ/IgG, A κ, λ). On the other hand, tumor cells in axillar node showed monoclonal cIg (IgG, κ). In the nodes of HD, there were small number of medium sized cells, which had a nucleus with prominent nucleolus and dispersed chromatin and were positive for B cell markers (B1, MB1) and polyclonal cIgs (IgG, A, κ/IgG, κ λ). LeuM1 was not detected in H cells, RS cells and diffuse lymphoma cells. This case was suggestive that some sort of HD was of lymphocyte origin and has some possibilities to develop a simultaneous progression to diffuse lymphoma.
何杰金氏病和非何杰金氏淋巴瘤的病例,发生在不同的解剖部位同时发病。
本文报道一例38岁日本男性合并何杰金氏病(HD)和非何杰金氏淋巴瘤(NHD)的不协调恶性淋巴瘤。1985年12月25日起,有轻度发热(38℃),全身乏力。术后腋窝及腹股沟淋巴结肿大。由于全身淋巴结肿胀伴贫血,他于2周后在永井市医院住院。切除颈部、腋窝及腹股沟淋巴结。他接受了化疗(Adr, End)。珠江三角洲。L-Asp)。6个月后,他被转移到山形县中心医院。尽管接受了化疗,他还是于1986年1月死于临床上可疑的消化道穿孔。尸体解剖是不允许的。切除宫颈及腹股沟淋巴结可见分散的单核霍奇金(H)细胞和多核里德-斯特伯格(RS)细胞,淋巴细胞、嗜酸性粒细胞和浆细胞混杂,诊断为HD,混合细胞型(MC)。腋窝结表现为小、大单核细胞弥漫性增生,核仁突出,无诊断性H细胞和/或RS细胞,诊断为NHL,弥漫性,混合性。免疫组化结果显示,宫颈和腹股沟淋巴结部分H细胞和RS细胞B1、MB1和多克隆IgG (IgG、A、κ/IgG、A κ、λ)阳性。另一方面,腋窝淋巴结肿瘤细胞表达单克隆IgG, κ。HD淋巴结中有少量中等大小细胞,细胞核核仁突出,染色质分散,B细胞标记物(B1、MB1)和多克隆IgG (IgG、a、κ/IgG、κ λ)阳性。H细胞、RS细胞和弥漫性淋巴瘤细胞均未检测到LeuM1。这个病例提示某种HD是淋巴细胞起源的,并且有可能同时发展为弥漫性淋巴瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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