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肾上腺外嗜铬细胞瘤伴严重血尿及排尿后头痛，一种罕见膀胱肿瘤实体的病例报告

Extraadrenal pheochromocytoma presenting with severe hematuria and postmicturition cephalgia, a case report of a rare bladder tumor entity.

作者信息

Sonderer Julian, Krull Ina, Schmid Hans-Peter, Müllhaupt Gautier

机构信息

Department of Urology, Institute for Medicine, University St.Gallen, Rorschacher Strasse 95, 9000, St.Gallen, Switzerland.

Department of Endocrinology, Institute for Medicine, University St.Gallen, Rorschacher Strasse 95, 9000, St.Gallen, Switzerland.

出版信息

Urol Case Rep. 2022 Jul 18;44:102170. doi: 10.1016/j.eucr.2022.102170. eCollection 2022 Sep.

DOI:10.1016/j.eucr.2022.102170
PMID:35935119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9350861/
Abstract

Paraganglioma (PGL) of the urinary bladder are a very rare tumor entity. Treatment of a PGL requires a multidisciplinary approach. We report on a case of a malignant pheochromocytoma (PHEO) of the bladder in a male adult due to a succinate dehydrogenase B (SDHB) subunit gene mutation where a partial cystectomy was perfomed after preoperative alpha blocking.

摘要

膀胱副神经节瘤（PGL）是一种非常罕见的肿瘤类型。PGL的治疗需要多学科方法。我们报告一例成年男性因琥珀酸脱氢酶B（SDHB）亚基基因突变导致的膀胱恶性嗜铬细胞瘤（PHEO）病例，该患者在术前进行α受体阻滞剂治疗后接受了部分膀胱切除术。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7b/9350861/07d2ebd5c5f1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7b/9350861/b1c01caf2675/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7b/9350861/07d2ebd5c5f1/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7b/9350861/b1c01caf2675/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc7b/9350861/07d2ebd5c5f1/gr2.jpg

相似文献

1
Extraadrenal pheochromocytoma presenting with severe hematuria and postmicturition cephalgia, a case report of a rare bladder tumor entity.肾上腺外嗜铬细胞瘤伴严重血尿及排尿后头痛，一种罕见膀胱肿瘤实体的病例报告
Urol Case Rep. 2022 Jul 18;44:102170. doi: 10.1016/j.eucr.2022.102170. eCollection 2022 Sep.
2
SDHB-related pheochromocytoma and paraganglioma penetrance and genotype-phenotype correlations.与琥珀酸脱氢酶亚基B相关的嗜铬细胞瘤和副神经节瘤的外显率及基因型-表型相关性
J Cancer Res Clin Oncol. 2017 Aug;143(8):1421-1435. doi: 10.1007/s00432-017-2397-3. Epub 2017 Apr 3.
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Increased expression of Nrf2 and elevated glucose uptake in pheochromocytoma and paraganglioma with SDHB gene mutation.SDHB 基因突变所致嗜铬细胞瘤和副神经节瘤中 Nrf2 的表达增加和葡萄糖摄取增加。
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引用本文的文献

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AME Case Rep. 2024 Sep 5;8:113. doi: 10.21037/acr-24-50. eCollection 2024.
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[Paraganglioma of the urinary bladder-a rare, but relevant differential diagnosis].[膀胱副神经节瘤——一种罕见但需鉴别的相关诊断]
Urologie. 2024 Feb;63(2):168-170. doi: 10.1007/s00120-023-02221-2. Epub 2023 Oct 24.
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Resection of Retroperitoneal Extra-Adrenal Pheochromocytoma: A Case Report.腹膜后肾上腺外嗜铬细胞瘤切除术：一例报告

本文引用的文献

1
Pheochromocytoma of the urinary bladder: a systematic review of the contemporary literature.膀胱嗜铬细胞瘤：当代文献的系统综述
BMC Urol. 2013 Apr 29;13:22. doi: 10.1186/1471-2490-13-22.
2
The succinate dehydrogenase genetic testing in a large prospective series of patients with paragangliomas.在一系列大量前瞻性嗜铬细胞瘤患者中进行琥珀酸脱氢酶基因检测。
J Clin Endocrinol Metab. 2009 Aug;94(8):2817-27. doi: 10.1210/jc.2008-2504. Epub 2009 May 19.
3
Pheochromocytoma of the urinary bladder.膀胱嗜铬细胞瘤
Cureus. 2023 Aug 9;15(8):e43185. doi: 10.7759/cureus.43185. eCollection 2023 Aug.
N Engl J Med. 1953 Jul 2;249(1):25-6. doi: 10.1056/NEJM195307022490106.
4
Understanding catecholamine metabolism as a guide to the biochemical diagnosis of pheochromocytoma.将儿茶酚胺代谢作为嗜铬细胞瘤生化诊断的指导依据。
Rev Endocr Metab Disord. 2001 Aug;2(3):297-311. doi: 10.1023/a:1011572617314.
5
Occurrence of pheochromocytoma in Rochester, Minnesota, 1950 through 1979.1950年至1979年明尼苏达州罗切斯特市嗜铬细胞瘤的发病情况。
Mayo Clin Proc. 1983 Dec;58(12):802-4.