Case Report: Two highly unusual adrenal tumors presenting with hypertension: a giant cystic pheochromocytoma with an ipsilateral large renal parapelvic cyst and a giant adrenal myelolipoma.

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Frontiers in Cardiovascular Medicine Pub Date : 2025-03-04 eCollection Date: 2025-01-01 DOI:10.3389/fcvm.2025.1541880
Ali Hakan Konuş, Kader Uğur, Erhan Aygen, Cihat Tektaş, Fatih Durumlu, Muhammet Çalık
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引用次数: 0

Abstract

Background: Giant cystic pheochromocytoma and giant adrenal myelolipoma are two highly uncommon masses. There are difficulties in diagnosis and management of both types of giant (>20 cm) adrenal tumors.

Case 1: A 56-year-old male patient applied with complaints of headache and high blood pressure. A mass was palpated in the left upper quadrant. The average 24-hour ambulatory blood pressure was 146/93 mm Hg. Computed tomography revealed a huge left adrenal cystic mass measuring 22 × 17 cm. A large left renal parapelvic cyst measuring 6 × 5.5 cm was also observed. Urine metanephrine and normetanephrine values were high. The patient was diagnosed with pheochromocytoma. It was decided to remove the adrenal cystic mass and renal parapelvic cyst with open surgery. Severe hypotension occurred during the intraoperative and early postoperative periods, and severe orthostatic dizziness occurred during the in-hospital stay and two months of outpatient follow-up. The patient's urine metanephrine and normetanephrine levels returned to normal. The average 24 h ambulatory blood pressure was 122/69 at six months.

Case 2: A 53-year-old male patient was admitted with complaints of high blood pressure, accompanied by mild headache and dizziness that had been ongoing for several months. A mass was palpated in the right upper quadrant. The average 24 h ambulatory blood pressure was 151/91 mm Hg. Abdominal computed tomography revealed a 24 × 16 × 22 cm solid mass with diffuse fat density originating from the right adrenal gland. Laboratory studies and endocrine investigations were normal. With the diagnosis of adrenal myelolipoma, a mass weighing 4,229 g was surgically removed. The patient was normotensive without medical treatment during the two-year follow-up after the operation.

Conclusion: To our knowledge, our case of giant cystic pheochromocytoma accompanied by ipsilateral large renal parapelvic cyst, which is the first in the literature, reports the management of severe hypotension in the perioperative period and severe orthostatic dizziness in the two-month follow-up. Non-functional adrenal myelolipomas can cause hypertension with mass effect. Our second case is one of the largest adrenal myelolipomas in literature. Although surgical removal of giant masses is difficult, successful surgeries have resulted in resolution of hypertension in our cases at mid-term follow-up.

病例报告:两个非常不寻常的肾上腺肿瘤表现为高血压:一个巨大的囊性嗜铬细胞瘤伴同侧肾盆腔旁大囊肿和一个巨大的肾上腺骨髓脂肪瘤。
背景:巨大囊性嗜铬细胞瘤和巨大肾上腺骨髓瘤是两种非常罕见的肿瘤。两种类型的巨大肾上腺肿瘤(> - 20cm)的诊断和治疗都存在困难。病例1:男性,56岁,主诉头痛、高血压。在左上腹触诊肿块。平均24小时动态血压146/93毫米汞柱。计算机断层扫描显示一个巨大的左肾上腺囊性肿块,大小为22 × 17厘米。左肾盆腔旁大囊肿,大小6 × 5.5 cm。尿中肾上腺素和去甲肾上腺素偏高。患者被诊断为嗜铬细胞瘤。我们决定采用开放手术切除肾上腺囊性肿块和肾盆腔旁囊肿。术中及术后早期出现严重低血压,住院及门诊随访2个月出现严重的直立性头晕。患者尿中肾上腺素和去甲肾上腺素恢复正常。6个月时平均24小时动态血压为122/69。病例2:患者男,53岁,以高血压主诉入院,伴轻度头痛、头晕,已持续数月。右上腹触诊肿块。平均24小时动态血压为151/91 mm Hg。腹部计算机断层扫描显示一个24 × 16 × 22 cm的实性肿块,伴有来自右侧肾上腺的弥漫性脂肪密度。实验室检查和内分泌检查均正常。由于诊断为肾上腺骨髓瘤,手术切除了重达4229 g的肿块。术后随访2年,患者血压正常,未接受药物治疗。结论:据我们所知,本病例为文献首次报道的巨大囊性嗜铬细胞瘤伴同侧肾盆腔旁大囊肿围手术期出现严重低血压,随访2个月出现严重直立性头晕。非功能性肾上腺骨髓瘤可引起高血压伴肿块效应。我们的第二个病例是文献中最大的肾上腺骨髓脂肪瘤之一。虽然手术切除巨大的肿块是困难的,但成功的手术使我们的病例在中期随访中高血压得到了解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.80
自引率
11.10%
发文量
3529
审稿时长
14 weeks
期刊介绍: Frontiers? Which frontiers? Where exactly are the frontiers of cardiovascular medicine? And who should be defining these frontiers? At Frontiers in Cardiovascular Medicine we believe it is worth being curious to foresee and explore beyond the current frontiers. In other words, we would like, through the articles published by our community journal Frontiers in Cardiovascular Medicine, to anticipate the future of cardiovascular medicine, and thus better prevent cardiovascular disorders and improve therapeutic options and outcomes of our patients.
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