Large and Extensive Multilocular Peritoneal Inclusion Cysts Lack Genomic Alterations and Follow an Indolent Clinical Course Despite Rare Recurrences.

IF 4.5 1区 医学 Q1 PATHOLOGY
American Journal of Surgical Pathology Pub Date : 2024-09-01 Epub Date: 2024-05-30 DOI:10.1097/PAS.0000000000002249
Kyle M Devins, Esther Baranov, Yin P Hung, Brendan C Dickson, Esther Oliva, Vikram Deshpande
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引用次数: 0

Abstract

Peritoneal inclusion cysts (PICs) are unilocular or multilocular cystic lesions lined by bland mesothelial cells. While most are small and localized, rare examples may be large or multifocal with diffuse peritoneal involvement, causing clinical and even pathologic concern for malignancy. We examined 20 PIC, including 8 large solitary and 12 multifocal lesions. Solitary PIC were found in 7 female and 1 male patients ranging from 19 to 55 (median: 37) years. Expanded collagenous (n=2) or edematous (n=1) areas were occasionally seen in the septae, and 1 had microscopic foci of myxoid stroma. Four had hobnail cells, and 1 had minor areas of papillary mesothelial hyperplasia. Multifocal PICs occurred in 9 female and 3 male patients ranging from 26 to 80 (median: 53) years. Three showed extensive associated fibrosis with entrapment of preexisting adipose tissue, 2 had areas resembling granulation tissue, and 3 had scattered foci of myxoid stroma. Hobnail cells were present in 9, papillary mesothelial hyperplasia in 2, entrapped single cells in 1, and 2 had areas resembling adenomatoid tumors. Two of the multifocal PICs had limited local recurrences at 18 and 21 months. No patients died of disease. Clonal alterations were not identified in any of the tested PICs (mutational and fusion analysis in 5, chromosomal microarray in 1). Despite limited local recurrences, we demonstrate that even large and multifocal PICs may lack identifiable genomic alterations and are associated with benign outcomes.

大而广的多发性腹膜包涵囊肿缺乏基因组变异,尽管罕见复发,但临床症状不明显。
腹膜包涵体囊肿(PIC)是由平滑肌间皮细胞衬里的单眼或多眼囊性病变。虽然大多数囊肿较小,且为局部病变,但罕见的囊肿可能较大或多灶,并累及弥漫性腹膜,从而引起临床甚至病理上对恶性肿瘤的担忧。我们检查了 20 例 PIC,包括 8 例大的单发病灶和 12 例多灶病灶。单发性 PIC 发现于 7 名女性和 1 名男性患者,年龄从 19 岁到 55 岁(中位数:37 岁)不等。隔膜中偶尔可见胶原扩张区(2 例)或水肿区(1 例),1 例显微镜下可见肌样基质灶。4 例出现梭形细胞,1 例出现轻微的乳头状间皮增生。多灶性 PICs 发生在 9 名女性和 3 名男性患者身上,患者年龄从 26 岁到 80 岁(中位数:53 岁)不等。其中 3 例表现为广泛的伴纤维化,并夹杂原有的脂肪组织,2 例有类似肉芽组织的区域,3 例有散在的类肌基质灶。9个病灶中存在梭形细胞,2个病灶中存在乳头状间皮增生,1个病灶中存在夹杂的单细胞,2个病灶中存在类似腺瘤的区域。其中两个多灶性 PIC 在 18 个月和 21 个月时出现局部局限性复发。没有患者死于疾病。在所有受检的 PIC 中均未发现克隆性改变(5 例进行了突变和融合分析,1 例进行了染色体芯片分析)。尽管局部复发率有限,但我们证明,即使是大的多灶性 PIC 也可能缺乏可识别的基因组改变,并与良性结果相关。
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来源期刊
CiteScore
10.30
自引率
5.40%
发文量
295
审稿时长
1 months
期刊介绍: The American Journal of Surgical Pathology has achieved worldwide recognition for its outstanding coverage of the state of the art in human surgical pathology. In each monthly issue, experts present original articles, review articles, detailed case reports, and special features, enhanced by superb illustrations. Coverage encompasses technical methods, diagnostic aids, and frozen-section diagnosis, in addition to detailed pathologic studies of a wide range of disease entities. Official Journal of The Arthur Purdy Stout Society of Surgical Pathologists and The Gastrointestinal Pathology Society.
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