Perinephric Myxoid Pseudotumor of Fat: A Series of 29 Cases Demonstrating Inconsistent Associations With Underlying Kidney Disease.

IF 4.2 1区 医学 Q1 PATHOLOGY
Azfar Neyaz, John S A Chrisinger, Dimitrios Korentzelos, Gayathri Devi Jalluri, Rana Naous, Abigail I Wald, Veronica Ulici, Sintawat Wangsiricharoen, Ali Alani, Douglas Rottmann, Carina A Dehner, Josephine K Dermawan, Kyle Perry, Ivy John
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引用次数: 0

Abstract

Perinephric myxoid pseudotumor of fat (PMPTF) is a recently characterized lesion typically associated with non-neoplastic renal disease. Its pathogenesis is thought to result from chronic renal "irritation," either due to mass effect from renal carcinoma or inflammation related to benign renal conditions. Prompted by several cases arising in the absence of underlying renal pathology, we conducted a multi-institutional study of 29 mass-forming cases with detailed clinical, histologic, and molecular characterization. We also reviewed 79 published cases to place our findings in a broader context. Histologic slides were reviewed for morphologic and immunohistochemical features. Clinical and follow-up data were obtained through retrospective chart review. The mean age was 67 years (range: 35 to 82), with a strong male predominance (M:F=13.5:1). The average tumor size was 10.3 cm. Liposarcoma was the most common initial diagnosis (n=20). Twelve patients (42%) had non-neoplastic renal disease, 7 (24%) had both non-neoplastic disease and renal cell carcinoma, one (3%) had renal cell carcinoma only, and 9 (31%) had no renal pathology. Histologically, lesions showed mature fat with scattered bland spindle to stellate cells, chronic inflammation, lymphoid aggregates, myxoid change, fat necrosis, hemosiderin, and prominent vasculature; extramedullary hematopoiesis was rare. All tested 28 cases were negative for MDM2 amplification by FISH. Comprehensive targeted NGS (Oncomine) and whole transcriptome sequencing (n=4) did not reveal any pathogenic alterations. Follow-up (n=28; mean, 20 months) showed stable or no disease in 24 cases; 3 patients died of unrelated causes, and one from postoperative complications. PMPTF is a benign, mass-forming lesion that mimics malignancy, particularly well-differentiated liposarcoma. Its occurrence in patients without identifiable renal pathology suggests alternative etiologies. Lack of genomic alterations supports its non-neoplastic nature. Accurate recognition is critical to prevent overtreatment. PMPTF may represent an early-stage reactive process within a broader spectrum of adipose tissue remodeling that includes renal replacement lipomatosis.

肾周脂肪黏液样假瘤:29例与潜在肾脏疾病不一致的关联
肾周黏液样假性脂肪瘤(PMPTF)是一种新发现的病变,通常与非肿瘤性肾脏疾病相关。其发病机制被认为是由慢性肾脏“刺激”引起的,要么是由于肾癌的肿块效应,要么是与良性肾脏疾病相关的炎症。由于一些病例出现在没有潜在肾脏病理的情况下,我们对29例肿块形成病例进行了多机构研究,并进行了详细的临床、组织学和分子特征分析。我们还回顾了79个已发表的案例,将我们的发现置于更广泛的背景下。检查组织切片的形态学和免疫组织化学特征。通过回顾性图表复习获得临床和随访资料。平均年龄67岁(35 ~ 82岁),男性居多(M:F=13.5:1)。肿瘤平均大小为10.3 cm。脂肪肉瘤是最常见的初始诊断(n=20)。12例(42%)有非肿瘤性肾脏疾病,7例(24%)同时有非肿瘤性肾脏疾病和肾细胞癌,1例(3%)仅有肾细胞癌,9例(31%)无肾脏病理。组织学上,病变表现为成熟脂肪伴散在的淡色梭形到星状细胞,慢性炎症,淋巴样聚集,粘液样改变,脂肪坏死,含铁血黄素,血管突出;髓外造血罕见。28例经FISH检测的MDM2扩增均为阴性。综合靶向NGS (Oncomine)和全转录组测序(n=4)未发现任何致病改变。随访28例,平均20个月,24例病情稳定或无疾病;3例死于无关原因,1例死于术后并发症。PMPTF是一种良性肿块状病变,类似恶性肿瘤,尤其是高分化脂肪肉瘤。它发生在没有明确肾脏病理的患者中,提示有其他病因。缺乏基因组改变支持其非肿瘤性质。准确识别是防止过度治疗的关键。PMPTF可能代表了更广泛的脂肪组织重塑的早期反应过程,包括肾脏替代脂肪瘤病。
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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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