一例青春期女孩肾鞘瘤:组织病理学观察与文献复习。

IF 0.6 4区 医学 Q4 PATHOLOGY
Fetal and Pediatric Pathology Pub Date : 2025-09-01 Epub Date: 2025-08-09 DOI:10.1080/15513815.2025.2543743
Keya Basu, Shristi Butta, Ayush Agarwal, Arijit Singha, Shyamalendu Medda, Debansu Sarkar, Uttara Chatterjee
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引用次数: 0

摘要

背景:肾鞘瘤是一种罕见的肾间质肿瘤。它的特点是肾素分泌和伴有低血钾的不可控高血压。病例报告:在这里我们报告一个15岁的女孩谁提出顽固性高血压,肌肉无力和疲劳。诊断检查显示严重的低钾血症,代谢性碱中毒和血浆肾素活性升高,醛固酮水平升高。肾动脉多普勒检查排除肾动脉狭窄,发现左侧肾肿块。行单纯肾切除术,组织病理学和免疫组织化学检查与肾瘤的诊断一致。电镜显示细胞质中肾素结晶,从而证实了诊断。结论:本报告强调了在青少年继发性高血压的鉴别诊断中包括肾膜瘤的重要性。此外,组织病理学和电子显微镜对肾瘤的诊断很重要,因为有几种肾肿瘤具有分泌肾素的活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reninoma in an Adolescent Girl: Histopathological Insights with Review of Literature.

Background: Reninoma is an uncommon mesenchymal tumor of the kidney. It is characterized by renin secretion and uncontrollable hypertension with associated hypokalemia. Case report: Here we report a case in a 15-year-old girl who presented with refractory hypertension, muscle weakness, and fatigue. Diagnostic workup revealed severe hypokalemia, metabolic alkalosis and elevated plasma renin activity with raised aldosterone levels. Renal artery doppler done to exclude renal artery stenosis, revealed a left sided renal mass. Simple nephrectomy was done and histopathological and immunohistochemical examination were consistent with a diagnosis of reninoma. Electron microscopy revealed renin crystals in the cytoplasm, thus confirming the diagnosis. Conclusion: This report underscores the importance of including reninoma in the differential diagnosis of secondary hypertension in an adolescent. Additionally, insights into histopathology and electron microscopy are important for the diagnosis of reninoma as there are several renal tumors that have renin-secreting activity.

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来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
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