肝实质中的原发性卡斯特曼病:病例报告和文献综述

iRadiology Pub Date : 2024-04-15 DOI:10.1002/ird3.74
Hanjun Zhang, Mingyue Song, Mingzhan Du, Zhuxue Zhang, Weiguo Zhang
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A maximum standardized uptake value (SUV<sub>max</sub>) of 3.270 and a delayed SUV<sub>max</sub> of 4.887 were recorded on <sup>18</sup>F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) scans (Figure 2a–d). The plasma cell variant of Castleman's disease was confirmed pathologically after left hemihepatectomy. Immunohistochemical analysis showed lymphoid hyperplasia, positive immunostaining for CD markers, and a Ki-67 index of 40% (Figure 2e,f). No recurrence has been noted on annual computed tomography scans after the 6-month follow-up.</p><p>Castleman's disease, also known as angiofollicular lymph node hyperplasia and giant lymph node hyperplasia [<span>1</span>], rarely arises in the hepatic parenchyma. Clinically, Castleman's disease can be divided into unicentric (UCD) and multicentric (MCD). 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摘要

一名 65 岁的妇女在一次常规体检中通过超声波检查发现肝脏 IV 段实质内有一个占位性病变。她没有病毒性肝炎或任何传染病病史,肿瘤标志物和常规血液生化指标正常。钆醋酸增强磁共振成像显示病灶轮廓清晰,T1加权像显示均匀低密度,T2加权像显示高密度伴晕征(图1a,b)。弥散加权成像显示均匀的弥散受限(图1c、d),动态对比增强成像显示动脉期高密度,肝胆期无Gd-EOB-DTPA摄取(图1e-g)。18F-氟脱氧葡萄糖正电子发射断层扫描/计算机断层扫描(FDG-PET/CT)显示最大标准化摄取值(SUVmax)为3.270,延迟SUVmax为4.887(图2a-d)。左半肝切除术后病理证实为浆细胞变异型卡斯特曼病。免疫组化分析显示淋巴细胞增生,CD标记免疫染色阳性,Ki-67指数为40%(图2e,f)。卡斯特曼病又称血管滤泡性淋巴结增生和巨淋巴结增生[1],很少发生在肝实质。临床上,卡斯特曼病可分为单中心型(UCD)和多中心型(MCD)。根据世界卫生组织第五版血液淋巴肿瘤分类,UCD 和特发性 MCD 被归类为以 B 细胞为主的肿瘤样病变[2, 3]。由于缺乏特异性的影像学特征,肝UCD的诊断仍然很困难。在我们的病例中,考虑到T2加权图像上存在光环征,有必要排除血管内皮瘤的可能性。然而,我们的患者并不具备血管内皮瘤的特征,如 "囊回缩 "征[5]。在动态增强磁共振成像中,该病灶的冠状强化可与肝细胞癌(HCC)相混淆。值得注意的是,我们病例中出现的日冕样强化和晕轮征也可能出现在肝细胞腺瘤中。然而,该病灶在相位外成像中未显示环状征或信号消失,也未摄取肝细胞特异性造影剂[7]。此外,我们病例中的病变在肝胆期显示出低信号,这排除了局灶性结节增生的可能[8, 9]。我们病例中的病变在弥散加权成像中显示出明显的高密度,其表观弥散系数值为 0.850 × 10-3,这通常表明是淋巴瘤或 HCC 等细胞丰富的病变[10-12]。我们病例中的病灶在 18F-FDG PET/CT 上显示中度代谢,SUVmax 为 3.270,这可能预示着恶性肿瘤,但也不能排除结核瘤或肉芽肿等炎症或肉芽肿性疾病。[13]虽然卡斯特曼病患者 PET/CT 的这一阳性发现尚未得到阐明,但其中一个解释可能是 UCD 的细胞增殖率高于正常肝细胞,但慢于恶性肿瘤细胞。UCD 病变中的 FDG 摄取现象已有文献报道[14-17]。总之,肝实质 UCD 极其罕见,且无特异性特征,这给放射科医生的术前诊断带来了挑战。然而,磁共振成像上的某些成像特征,如晕征、弥散受限、冠状动脉样强化以及18F-FDG PET/CT上的适度代谢可能有助于UCD与其他肝病的鉴别,这可能有助于临床上对患者的护理。宋明月参与了研究的构思和设计,张竹雪对手稿进行了建设性的修改;杜明展参与了数据的收集和整理;张卫国全程参与并指导了研究,二人共享通讯作者身份。所有作者都对之前的手稿版本发表了意见,并批准了最终版本。作者声明没有利益冲突。
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Primary Castleman's disease in the hepatic parenchyma: A case report and literature review

A 65-year-old woman was found to have a space-occupying lesion in the parenchyma of hepatic segment IV by ultrasonography during a routine medical checkup. She had no history of viral hepatitis or any infectious diseases, and her tumor markers and routine blood and biochemical indices were normal. Gadoxetic acid-enhanced magnetic resonance imaging revealed a well-defined lesion that showed homogeneous hypointensity on T1-weighted images and hyperintensity with a halo sign on T2-weighted images (Figure 1a,b). Diffusion-weighted imaging showed homogeneous restricted diffusion (Figure 1c,d), and dynamic contrast-enhanced imaging showed hyperintensity in the arterial phase with no Gd-EOB-DTPA uptake in the hepatobiliary phase (Figure 1e–g). A maximum standardized uptake value (SUVmax) of 3.270 and a delayed SUVmax of 4.887 were recorded on 18F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) scans (Figure 2a–d). The plasma cell variant of Castleman's disease was confirmed pathologically after left hemihepatectomy. Immunohistochemical analysis showed lymphoid hyperplasia, positive immunostaining for CD markers, and a Ki-67 index of 40% (Figure 2e,f). No recurrence has been noted on annual computed tomography scans after the 6-month follow-up.

Castleman's disease, also known as angiofollicular lymph node hyperplasia and giant lymph node hyperplasia [1], rarely arises in the hepatic parenchyma. Clinically, Castleman's disease can be divided into unicentric (UCD) and multicentric (MCD). UCD and idiopathic MCD are classified into tumor-like lesions with B-cell predominance according to the fifth edition of the World Health Organization classification of haematolymphoid tumors [2, 3].

UCD usually presents as a localized lesion without any obvious symptoms [4]. Diagnosis of hepatic UCD remains difficult because of a lack of specific imaging features. In our case, it was necessary to rule out the possibility of hemangioendothelioma in view of the presence of a halo sign on T2-weighted images. However, our patient had none of the hallmarks of hemangioendothelioma, such as the “capsular retraction” sign [5]. On dynamic enhanced magnetic resonance imaging, the corona-like enhancement of this lesion can be confused with hepatocellular carcinoma (HCC). Nevertheless, the lesion lacked a capsule and the classical “wash in and wash out” dynamic enhancement pattern typical of HCC [6].

Of note, the corona-like enhancement and the halo sign seen in our case may also be seen in hepatocellular adenoma. However, the lesion did not show the atoll sign or signal drop out on out-of-phase imaging or uptake of a hepatocyte-specific contrast agent [7]. Furthermore, the lesion in our case showed a low signal in the hepatobiliary phase, which rules out focal nodular hyperplasia [8, 9].

The lesion in our case showed remarkable hyperintensity on diffusion-weighted imaging and had an Apparent Diffusion Coefficient value of 0.850 × 10−3, which generally indicates a cell-rich lesion like lymphoma or HCC [10-12]. More cases need to be collected to address this relatively specific feature in the diagnosis of UCD.

The lesion in our case showed moderate metabolism on 18F-FDG PET/CT with an SUVmax of 3.270, which may indicate malignancy, although inflammatory or granulomatous disease such as tuberculoma or granuloma cannot be ruled out. [13] Although this positive finding on PET/CT in a patient with Castleman's disease has yet to be elucidated, one of the explanations may be that the cell proliferation rate is higher for UCD than for normal hepatocytes but slower than for malignant tumor cells. The phenomenon of FDG uptake in UCD lesions has been reported in literature [14-17]. Metastasis could be excluded in our patient because of the lack of marked glucose uptake at other sites, including lymph nodes.

In conclusion, UCD in the hepatic parenchyma is extremely rare and has no specific features, which makes preoperative diagnosis challenging for radiologists. However, certain imaging characteristics on magnetic resonance imaging, such as the halo sign, restricted diffusion, and corona-like enhancement as well as moderate metabolism on 18F-FDG PET/CT may facilitate the differentiation of UCD from other hepatic conditions, which may be helpful for patient care in the clinical setting.

Hanjun Zhang analyzed the data and prepared the first draft of the manuscript. Mingyue Song participated in the conception and design of the study, Zhuxue Zhang constructively revised the manuscript; Mingzhan Du participated in data collection and organization; Weiguo Zhang participated in and supervised the study throughout, and they share corresponding authorship. All authors commented on previous versions of the manuscript and approved the final version.

The authors declare no conflicts of interest.

Not applicable.

Not applicable.

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