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移植物抗宿主病——11例经活检证实病例的临床与病理分析

Graft-versus-host disease--clinical and pathological analysis of 11 biopsy proven cases.

作者信息

Kim K M, Han K J, Kang C S, Shim S I

机构信息

Catholic University Medical College, Department of Clinical Pathology.

出版信息

J Korean Med Sci. 1994 Oct;9(5):382-7. doi: 10.3346/jkms.1994.9.5.382.

Abstract

Graft-versus-host disease (GVHD) is a life threatening complication that may occur following allogenic bone marrow transplantation (BMT) in the patients with aplastic anemia, leukemia or genetic immunodeficiency. It has been known that GVHD occurs approximately 70% of recipients of BMT in western countries but no definite incidence has been reported in Korea. In our St. Mary's Hospital, GVHD occurs in about 30% of BMT recipients. Histopathologically the acute phase skin shows diffuse lymphocytic infiltrates in the upper dermis with extensive exocytosis. Scattered throughout the epidermis are many degenerated keratinocytes, which are often associated with one or more satellite lymphocytes (satellite cell necrosis). In the chronic phase, acanthosis, eosinophilic keratinocytes resembling colloid bodies and mononuclear cell infiltrates in the upper dermis are noted. We reviewed 5 cases of acute GVHD and 6 cases of chronic GVHD. All patients received allogenic BMT from Jan. 1, 1992 to July 1, 1993. Ten patients were male and one was female. The mean age was 34 (20-70). The pathologic diagnosis was 3 cases of CML, 2 of ALL, 2 of AML (FAB M2), 2 of aplastic anemia, 1 of CLL and 1 of AML (FAB M5). The interval from BMT to GVHD varied from 14 days to 4 years (median 220 days). The skin and GI tract were involved in all eleven cases. Ten cases were histologically proven by skin biopsies, and two cases by salivary gland and colonic biopsies, respectively. The histological findings of the skin, salivary gland and colonic biopsieds were described. Immunohistochemical stain of the skin was done using CD4, CD8, HLA DR and Leu 7 antibodies.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

移植物抗宿主病(GVHD)是一种危及生命的并发症,可发生于再生障碍性贫血、白血病或遗传性免疫缺陷患者接受异基因骨髓移植(BMT)之后。已知在西方国家,约70%的BMT受者会发生GVHD,但韩国尚未报道确切的发病率。在我们的圣玛丽医院,约30%的BMT受者会发生GVHD。组织病理学上,急性期皮肤表现为真皮上部弥漫性淋巴细胞浸润伴广泛的细胞外渗。整个表皮散在许多变性的角质形成细胞,常伴有一个或多个卫星淋巴细胞(卫星细胞坏死)。慢性期可见棘皮症、类似胶样小体的嗜酸性角质形成细胞以及真皮上部的单核细胞浸润。我们回顾了5例急性GVHD和6例慢性GVHD病例。所有患者在1992年1月1日至1993年7月1日期间接受了异基因BMT。10例为男性,1例为女性。平均年龄为34岁(20 - 70岁)。病理诊断为3例慢性粒细胞白血病、2例急性淋巴细胞白血病、2例急性髓细胞白血病(FAB M2)、2例再生障碍性贫血、1例慢性淋巴细胞白血病和1例急性髓细胞白血病(FAB M5)。从BMT到GVHD的间隔时间从14天到4年不等(中位值220天)。11例均累及皮肤和胃肠道。10例经皮肤活检组织学确诊,2例分别经唾液腺和结肠活检确诊。描述了皮肤、唾液腺和结肠活检的组织学发现。使用CD4、CD8、HLA DR和Leu 7抗体对皮肤进行了免疫组织化学染色。(摘要截取自250字)

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