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骨髓性白血病的皮肤受累:皮肤浸润的形态学和免疫表型异质性

Skin involvement in myelogenous leukemia: morphologic and immunophenotypic heterogeneity of skin infiltrates.

作者信息

Kaiserling E, Horny H P, Geerts M L, Schmid U

机构信息

Institute of Pathology, University of Tübingen, Germany.

出版信息

Mod Pathol. 1994 Sep;7(7):771-9.

PMID:7824512
Abstract

A systematic morphological analysis of cutaneous infiltrates in acute myelogenous leukemia and myelodysplastic syndrome revealed that in many cases the infiltrating cells have a different phenotype from those in the bone marrow. This study sought to answer two questions: (a) How wide is the range of cytological features and immunoreactivity of the cutaneous infiltrates and what danger is there of misinterpretation? (b) What are the possible causes of the wide spectrum of differentiation of the cells infiltrating the skin? Skin biopsy specimens from 16 patients with myelogenous leukemia or myelodysplastic syndrome were investigated. The diagnosis was acute myelomonocytic leukemia (M4, according to the French-American-British/FAB system of classification of acute leukemias) in eight cases, acute monocytic leukemia (M5) in four cases, aleukemic leukemia cutis as a recurrence of M2 leukemia after treatment in one case, and myelodysplastic syndrome in three cases, including one case of myelodysplasia with an excess of bone marrow blasts (RAEB-T) and two cases of chronic myelomonocytic leukemia, one of which presented as aleukemic leukemia cutis. Reactivity with the macrophage-associated antibodies anti-CD68, Ki-M1p, and anti-lysozyme was the most consistent. However, the naphthol AS-D chloroacetate esterase reaction and staining with DAKO-M1, Ki-My2p, anti-neutrophil elastase, and anti-CD34 were found to be of little value for identifying the cutaneous infiltrate as myelogenous. Some antibodies (e.g., anti-S100 protein and MB2) even produced staining in a few cases that could have led to a mistaken diagnosis of histiocytic neoplasm or malignant lymphoma.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对急性髓性白血病和骨髓增生异常综合征皮肤浸润的系统形态学分析显示,在许多病例中,浸润细胞的表型与骨髓中的不同。本研究旨在回答两个问题:(a)皮肤浸润的细胞学特征和免疫反应性范围有多广,误诊的风险有多大?(b)浸润皮肤的细胞广泛分化的可能原因是什么?对16例髓性白血病或骨髓增生异常综合征患者的皮肤活检标本进行了研究。诊断为急性粒单核细胞白血病(根据法国-美国-英国/FAB急性白血病分类系统为M4)8例,急性单核细胞白血病(M5)4例,1例M2白血病治疗后复发的无白血病性白血病性皮肤,3例骨髓增生异常综合征,包括1例骨髓原始细胞过多的骨髓增生异常(RAEB-T)和2例慢性粒单核细胞白血病,其中1例表现为无白血病性白血病性皮肤。与巨噬细胞相关抗体抗CD68、Ki-M1p和抗溶菌酶的反应最为一致。然而,发现萘酚AS-D氯乙酸酯酶反应以及用DAKO-M1、Ki-My2p、抗中性粒细胞弹性蛋白酶和抗CD34染色对将皮肤浸润识别为髓性浸润价值不大。一些抗体(如抗S100蛋白和MB2)甚至在少数病例中产生染色,可能导致组织细胞肿瘤或恶性淋巴瘤的误诊。(摘要截选至250词)

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