Department G.F. Ingrassia, Division of Anatomic Pathology, Policlinico-Vittorio Emanuele University Hospital, Catania, Italy.
Pathol Res Pract. 2011 May 15;207(5):322-6. doi: 10.1016/j.prp.2011.01.009. Epub 2011 Mar 2.
Although inflammatory pseudotumor (IPT) and inflammatory myofibroblastic tumor (IMT) may share a common morphology, they are distinct clinico-pathologic entities. Unfortunately, the terms IMT and IPT are still used interchangeably, especially when lesions occur in unusual sites, including breast. All the cases of IMT/IPT involving the breast have raised spontaneously without any apparent prior injury. We herein report the first case of a post-traumatic IPT of the breast parenchyma in a 22-year-old male. Histologically, the lesion was highly cellular and composed of spindle cells arranged in a predominant fascicular pattern. Notably, mono- or multi-nucleated large pleomorphic cells were observed. Inflammatory cells, especially plasma cells and lymphocytes, were closely admixed with the spindle cell proliferation. The overall picture was reminiscent of an "IMT with atypical features", typically seen in lung, abdomen, pelvis, and retroperitoneum of children. Immunohistochemically, the spindle-shaped and large pleomorphic cells were immunoreactive to vimentin, α-smooth muscle actin, and desmin. No immunoreactivity was obtained with ALK-1 protein. The present case contributes to widening the morphological spectrum of IPT of the breast, emphasizing the possibility that a reactive lesion may contain large pleomorphic cells that may represent a potential diagnostic pitfall. Lastly, we suggest that the diagnosis of IMT of the breast should be rendered with caution when dealing with ALK-negative spindle cell lesions in adult patients, and alternative diagnoses, including IPT, should be seriously considered.
虽然炎性假瘤 (IPT) 和炎性肌纤维母细胞瘤 (IMT) 可能具有共同的形态学特征,但它们是不同的临床病理实体。不幸的是,IMT 和 IPT 这两个术语仍在互换使用,尤其是在病变发生于不常见的部位时,包括乳房。所有发生于乳房的 IMT/IPT 病变均自发出现,无明显的先前损伤。我们在此报告首例发生于 22 岁男性乳房实质的创伤后 IPT。组织学上,病变细胞丰富,由排列成主要束状模式的梭形细胞组成。值得注意的是,观察到单核或多核的巨大多形性细胞。炎症细胞,尤其是浆细胞和淋巴细胞,与梭形细胞增生密切混合。整体表现类似于“具有非典型特征的 IMT”,通常见于儿童的肺、腹部、骨盆和腹膜后。免疫组织化学染色显示,梭形和巨大多形性细胞对波形蛋白、α-平滑肌肌动蛋白和结蛋白呈免疫反应性。ALK-1 蛋白无免疫反应性。本病例扩大了乳腺 IPT 的形态学谱,强调了反应性病变可能包含大的多形性细胞,这可能是一个潜在的诊断陷阱。最后,我们建议在处理成人 ALK 阴性梭形细胞病变时,应谨慎诊断乳腺 IMT,并应认真考虑包括 IPT 在内的其他诊断。