Department of Pathology, Vanderbilt University Medical Center, Nashville, TN 37232-2561, USA.
Mod Pathol. 2011 Apr;24(4):606-12. doi: 10.1038/modpathol.2010.226. Epub 2011 Feb 4.
Inflammatory myofibroblastic tumor is a rare mesenchymal neoplasm that harbors an anaplastic lymphoma kinase (ALK) gene rearrangement in the majority of cases. It is composed of fibroblastic-myofibroblastic cells with a characteristic inflammatory infiltrate that consists predominantly of plasma cells. In contrast, IgG4-related sclerosing disease is a recently described multisystem disorder with a histological appearance similar to inflammatory myofibroblastic tumor. The plasma cell infiltrate is characteristic in IgG4-related sclerosing disease and has been studied as a tool to render this diagnosis. Histologically, the two disorders overlap, although there are significant clinical differences. This study analyzes the histological appearance of 36 inflammatory myofibroblastic tumors, compares them with IgG4-related sclerosing disease, and assesses the plasma cell profile using immunohistochemistry to determine the range and proportion of IgG4 plasma cells. The majority of patients were children and young adults, mainly with solitary masses and no clinical manifestations of IgG4-related sclerosing disease. ALK-1 positivity was present in 23 cases (64%). None showed obliterative phlebitis or prominent lymphoid aggregates. Of 36 inflammatory myofibroblastic tumors, 15 cases showed an IgG4/IgG ratio ≥0.10, a cutoff described in the literature as supportive of IgG4-related sclerosing disease and up to 33 IgG4-positive plasma cells per high-power field indicating a mild-to-moderate increase as compared with IgG4-related sclerosing disease. Currently, the diagnostic recognition of inflammatory myofibroblastic tumor is based on clinicopathological features and diagnostic adjuncts, such as ALK-1 reactivity and genetic tests. Although inflammatory myofibroblastic tumor and IgG4-related sclerosing disease are distinct entities, a subset of inflammatory myofibroblastic tumors exhibit an IgG4/IgG ratio that is within the range for IgG4-related sclerosing disease. Therefore, the ratio alone cannot be used as a reliable discriminator between these two entities and other clinical and pathologic features must always be taken into account.
炎性肌纤维母细胞瘤是一种罕见的间叶性肿瘤,大多数病例存在间变性淋巴瘤激酶(ALK)基因重排。它由成纤维细胞-肌纤维母细胞组成,特征性炎症浸润主要由浆细胞组成。相比之下,IgG4 相关硬化性疾病是一种最近描述的多系统疾病,其组织学表现类似于炎性肌纤维母细胞瘤。浆细胞浸润是 IgG4 相关硬化性疾病的特征,并已被研究作为诊断该病的一种工具。从组织学上看,这两种疾病有重叠,但也有显著的临床差异。本研究分析了 36 例炎性肌纤维母细胞瘤的组织学表现,将其与 IgG4 相关硬化性疾病进行比较,并通过免疫组织化学评估浆细胞的表型,以确定 IgG4 浆细胞的范围和比例。大多数患者为儿童和青年,主要表现为单发肿块,无 IgG4 相关硬化性疾病的临床表现。23 例(64%)ALK-1 阳性。无一例出现闭塞性静脉炎或明显的淋巴样聚集。36 例炎性肌纤维母细胞瘤中,15 例 IgG4/IgG 比值≥0.10,该比值是文献中支持 IgG4 相关硬化性疾病的截断值,与 IgG4 相关硬化性疾病相比,高倍镜下每有 33 个 IgG4 阳性浆细胞表明存在轻度至中度增加。目前,炎性肌纤维母细胞瘤的诊断识别基于临床病理特征和辅助诊断方法,如 ALK-1 反应性和基因检测。虽然炎性肌纤维母细胞瘤和 IgG4 相关硬化性疾病是不同的实体,但有一部分炎性肌纤维母细胞瘤的 IgG4/IgG 比值在 IgG4 相关硬化性疾病的范围内。因此,仅比值不能作为这两种实体之间的可靠鉴别指标,还必须始终考虑其他临床和病理特征。