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伴有自发性出血的生化检查阴性嗜铬细胞瘤

Biochemically Negative Pheochromocytoma With Spontaneous Hemorrhage.

作者信息

Vincent Ashley B, Morales Evelyn J, Shahla Leena

机构信息

University of Arizona College of Medicine, Phoenix, Arizona.

Universidad Central del Caribe, Juanita, Bayamon, Puerto Rico.

出版信息

AACE Endocrinol Diabetes. 2025 May 26;12(2):93-96. doi: 10.1016/j.aed.2025.05.004. eCollection 2025 Jul-Aug.

Abstract

BACKGROUND/OBJECTIVE: Pheochromocytomas are neuroendocrine tumors that arise from adrenomedullary chromaffin cells that produce excess catecholamines. With advancements in imaging modalities, increasing numbers of incidental adrenal masses are discovered with pheochromocytomas making up approximately 4.2% of incidental adrenal masses. The objective of this report is to describe a patient with an unusual presentation of pheochromocytoma that was asymptomatic and lacked classic laboratory findings.

CASE REPORT

We present the case of a 31-year-old female who presented to the emergency department with abdominal pain and was found to have an adrenal mass on computed tomography scan. Biopsy of the mass was attempted multiple times prior to biochemical evaluation. The mass was later discovered to be a biochemically negative pheochromocytoma with spontaneous hemorrhage on histological examination following adrenal resection.

DISCUSSION

Pheochromocytomas are the most commonly reported adrenal mass found to have spontaneous hemorrhage. Between 9% and 32% of pheochromocytomas may be biochemically silent adding to the complexity of making an accurate diagnosis and calls into questions current perioperative management of all adrenal masses. In addition, this case serves as a reminder to complete biochemical evaluation prior to invasive adrenal procedures.

CONCLUSION

This case offers insight into challenges with diagnosis and management of pheochromocytoma with spontaneous hemorrhage, and encourages caution when evaluating adrenal masses due to risk of pheochromocytoma even when biochemically negative.

摘要

背景/目的:嗜铬细胞瘤是起源于肾上腺髓质嗜铬细胞的神经内分泌肿瘤,可产生过量儿茶酚胺。随着影像学技术的进步,发现的肾上腺意外瘤数量不断增加,嗜铬细胞瘤约占肾上腺意外瘤的4.2%。本报告的目的是描述一例表现不寻常的嗜铬细胞瘤患者,该患者无症状且缺乏典型的实验室检查结果。

病例报告

我们报告一例31岁女性患者,因腹痛就诊于急诊科,计算机断层扫描发现肾上腺肿块。在进行生化评估之前,多次尝试对肿块进行活检。该肿块后来被发现是一例生化检查阴性的嗜铬细胞瘤,肾上腺切除术后组织学检查显示有自发性出血。

讨论

嗜铬细胞瘤是最常报告的可发生自发性出血的肾上腺肿块。9%至32%的嗜铬细胞瘤可能在生化检查中无异常表现,这增加了准确诊断的复杂性,并对当前所有肾上腺肿块的围手术期管理提出了质疑。此外,该病例提醒我们在进行侵入性肾上腺手术之前要完成生化评估。

结论

本病例揭示了嗜铬细胞瘤合并自发性出血在诊断和治疗方面的挑战,并提醒我们在评估肾上腺肿块时要谨慎,因为即使生化检查阴性也存在嗜铬细胞瘤的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbab/12332488/511fddd7b10c/gr1.jpg

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