纤维化组织细胞型肝假瘤:一种抗生素反应性肿瘤。

Kshitij S Arora, Mark A Anderson, Azfar Neyaz, Osman Yilmaz, Amaya Pankaj, Cristina R Ferrone, Yoh Zen, Jonathan England, Vikram Deshpande
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引用次数: 3

摘要

炎性假瘤是一个术语,用于指定炎症丰富的肿瘤病变。在排除特定实体(如igg4相关疾病和先前包含在该实体中的其他肿瘤实体)后,大多数肝假肿瘤表现出突出的纤维组织细胞炎症反应,并且先前被归类为肝假肿瘤的纤维组织细胞变异型(FHVHPT)。本研究的目的是检查该实体的临床,放射学,组织学和病因学方面。在排除肿瘤疾病后,我们在2009年至2019年期间从3家机构确定了30例FHVHPT患者。我们提取了人口统计学和临床数据、肝功能测试、培养结果和放射学信息。苏木精和伊红染色玻片的炎症模式及其细胞组成进行了审查。所有病例均行免疫组化检测IgG4和IgG。30例以FHVHPT为特征的病变的平均年龄为56岁(范围:23至79岁)。19例为孤立性病变;11个是倍数。病灶平均大小为3.8 cm(范围:1 ~ 7.5 cm)。在影像学上,肿瘤进程或转移是主要的诊断考虑(n= 15.50%)。最常见的症状是腹痛(n=14/30);8例患者出现与感染过程相符的症状,包括发烧。炎性浸润以淋巴细胞和浆细胞为主,多数病例以组织细胞浸润为主(22/30)。中性粒细胞12例,微脓肿8例。14/30例呈故事状纤维化;闭塞性静脉炎未确诊。在评估的9个病例中,培养鉴定出4个微生物。平均IgG4计数为每HPF 9.3个(范围:0 - 51),26例活检中有9例(35%)显示每HPF >10个IgG4阳性浆细胞。IgG4与IgG的平均比值为8%(范围:8%至46%)。4例行肝切除术。使用广谱抗生素(n=14),病变消退或缩小。8例患者未接受特异性治疗,6例病变自行消退,2例保持稳定或缩小。值得注意的是,这些患者均未出现肝脏复发的迹象。FHVHPT是一种类似肝肿瘤的肿瘤性病变,其组织学特征是纤维组织细胞浸润。在大多数患者中,FHVHPT代表肝脓肿的组织阶段,可以通过抗生素治疗成功管理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fibrohistiocytic Variant of Hepatic Pseudotumor: An Antibiotic Responsive Tumefactive Lesion.

Inflammatory pseudotumor is a term used to designate inflammation-rich tumefactive lesions. Following the exclusion of specific entities such as IgG4-related disease and other neoplastic entities previously included in this entity, the majority of hepatic pseudotumors show a prominent fibrohistiocytic inflammatory reaction and have been previously categorized as fibrohistiocytic variant of hepatic pseudotumor (FHVHPT). The goal of this study was to examine the clinical, radiologic, histologic, and etiologic aspects of this entity. After excluding neoplastic diseases, we identified 30 patients with FHVHPT from 3 institutions between 2009 and 2019. We extracted demographic and clinical data, liver function tests as well as culture results and radiologic information. Hematoxylin and eosin-stained slides were reviewed for pattern of inflammation as well as its cellular composition. Immunohistochemistry for IgG4 and IgG was performed in all cases. The mean age of the 30 lesions characterized as FHVHPT was 56 years (range: 23 to 79 y). Nineteen patients showed solitary lesions; 11 were multiple. The mean size of the lesion was 3.8 cm (range: 1 to 7.5 cm). On imaging, a neoplastic process or metastasis was the leading diagnostic consideration (n=15, 50%). The most common symptom was abdominal pain (n=14/30); 8 patients presented with symptoms compatible with an infectious process, including fever. The inflammatory infiltrate was dominated by lymphocytes and plasma cells, and in most cases, a prominent histiocytic infiltrate (22/30). Neutrophils were identified in 12 cases, with microabscess noted in 8. Storiform pattern of fibrosis was seen in 14/30 cases; obliterative phlebitis was not identified. Culture identified a microorganism in 4 of 9 cases evaluated. The mean IgG4 count was 9.3 per HPF (range: 0 to 51) with 9 of the 26 (35%) biopsies showing >10 IgG4 positive plasma cells per HPF. The mean IgG4 to IgG ratio was 8% (range: 8% to 46%). A hepatectomy was performed in 4 cases. On broad spectrum antibiotics (n=14) the lesions either resolved or decreased in size. Eight patients did not receive specific therapy, nevertheless, the lesion(s) resolved spontaneously in 6 cases, remained stable or decreased in size in 2 cases. Notably, none of these patients showed evidence of a hepatic recurrence. FHVHPT, a tumefactive lesion that mimics hepatic neoplasia, is histologically characterized by a fibrohistiocytic infiltrate. In the majority of patients FHVHPT represents the organizing phase of hepatic abscess and can be successfully managed with antibiotic therapy.

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