儿科人群的局灶性结节增生:多中心经验。

IF 1.3 4区 医学 Q3 PATHOLOGY Pediatric and Developmental Pathology Pub Date : 2023-07-01 Epub Date: 2023-04-21 DOI:10.1177/10935266231167489
Iván A González, Donghai Wang, Maria Cristina Pacheco, Xuchen Zhang, Pierre Russo
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引用次数: 0

摘要

背景:局灶性结节性增生(FNH)是一种典型的年轻女性肝脏良性病变。在儿童中,FNH是罕见的,其详细的临床病理特征在很大程度上仍然未知。此外,没有研究将儿童FNH特征与成人FNH特征进行比较。方法:在本研究中,我们分析了47例儿童FNH病例(年龄范围:23岁) 天至18 年),并将其与31例成年患者(年龄范围:20-64岁)的FNH病例进行比较 结果:在儿科病例中,13例(28%)有既往恶性肿瘤史,其中4例接受了放化疗和干细胞移植(SCT)治疗,5例仅接受放化疗,3例接受了化疗和SCT治疗。在儿科病例中,41例(87%)有中心瘢痕,46例(98%)有纤维间隔。儿童和成人FNH在女性患者中更常见。儿科患者的病例也与较大的体型显著相关(P = .047),无营养不良血管(P = .001),无正弦曲线扩张(P = .029)、假腺泡形成(P = .013)和脂肪变性(P = .029)。结论:根据我们的经验,尽管大多数儿童FNH病例显示出成人的典型组织学特征,但仍存在一些显著差异,对这些发现的认识有助于评估这些罕见病例。
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Focal Nodular Hyperplasia in the Pediatric Population: A Multicenter Experience.

Background: Focal nodular hyperplasia (FNH) is a benign liver lesion classically presenting in young females. In children, FNH is rare and its detailed clinicopathologic characteristics remain largely unknown. Furthermore, there are no studies comparing pediatric FNH features to those presenting in adults.

Methods: In this study, we analyzed a total of 47 FNH cases in pediatric patients (age range: 23 days to 18 years) from 3 centers and compared them to a cohort of 31 FNH cases in adult patients (age range: 20-64 years).

Results: Of the pediatric cases, 13 cases (28%) had a history of a prior malignancy of which 4 were treated with chemoradiation and stem cell transplantation (SCT), 5 with chemoradiation alone and 3 with chemotherapy and SCT. In the pediatric cases 41 (87%) had a central scar and 46 (98%) had fibrous septa. Both pediatric and adult FNH were more common in female patients. Cases in pediatric patients were also significantly associated with larger size (P = .047), absence of dystrophic vessels (P = .001), absence of sinusoidal dilatation (P = .029), pseudoacini formation (P = .013), and steatosis (P = .029).

Conclusion: In our experience although most cases of pediatric FNH show the classic histologic features seen in adults, some significant differences exist, and awareness of these findings could aid in the evaluation of these rare cases.

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来源期刊
CiteScore
3.70
自引率
5.30%
发文量
59
审稿时长
6-12 weeks
期刊介绍: The Journal covers the spectrum of disorders of early development (including embryology, placentology, and teratology), gestational and perinatal diseases, and all diseases of childhood. Studies may be in any field of experimental, anatomic, or clinical pathology, including molecular pathology. Case reports are published only if they provide new insights into disease mechanisms or new information.
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