Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Division of Pathology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Am J Case Rep. 2024 Sep 7;25:e943875. doi: 10.12659/AJCR.943875.
BACKGROUND Pheochromocytomas, rare tumors arising from the adrenal medulla, can present with highly variable symptoms; therefore, pheochromocytomas frequently remain undiagnosed, leaving the potential for physiological complications. Acutely, these complications include pheochromocytoma crisis, in which high levels of catecholamines are released and cause a life-threatening hypertensive emergency. Over time, undiagnosed pheochromocytomas can lead to cardiovascular damage and end-organ disease related to chronic exposure to elevated blood pressure. CASE REPORT We share a case of pheochromocytoma in a 45-year-old woman who presented with gastrointestinal symptoms of intractable nausea, vomiting, and abdominal pain. Imaging revealed an adrenal mass that had radiographic features that were most consistent with myelolipoma. Before exposing the patient to anesthesia and endoscopy for further diagnostic workup of her gastrointestinal symptoms, which can trigger a catecholamine surge in individuals with a pheochromocytoma, further biochemical testing was performed. Testing of plasma and urine confirmed pheochromocytoma, and surgical resection was performed for definitive treatment. Ultimately, the patient had resolution of her symptoms following the removal of the tumor. CONCLUSIONS The resolution of symptoms following surgical resection suggests that symptoms may have been related to the mass effect of the tumor or as an atypical manifestation of increased catecholamine levels. Additionally, by screening for pheochromocytoma, the patient was able to avoid potential complications that can result from common gastroenterological diagnostic procedures. This case report highlights the potential benefit for screening for pheochromocytoma when faced with symptoms that may be non-specific or related to mass effect upon surrounding organs.
嗜铬细胞瘤,一种源自肾上腺髓质的罕见肿瘤,其症状表现具有高度可变性;因此,嗜铬细胞瘤经常未被诊断出来,从而存在潜在的生理并发症。急性情况下,这些并发症包括嗜铬细胞瘤危象,其中大量儿茶酚胺被释放并导致危及生命的高血压急症。随着时间的推移,未被诊断的嗜铬细胞瘤会导致心血管损伤和与慢性暴露于升高的血压相关的终末器官疾病。
我们分享了一例 45 岁女性嗜铬细胞瘤病例,她以难治性恶心、呕吐和腹痛等胃肠道症状就诊。影像学检查显示存在肾上腺肿块,其影像学特征最符合骨髓脂肪瘤。在为进一步诊断胃肠道症状(可能会引发嗜铬细胞瘤患者儿茶酚胺激增)对患者进行麻醉和内镜检查之前,进一步进行了生化检测。血浆和尿液检测证实了嗜铬细胞瘤的存在,并进行了手术切除以进行明确治疗。最终,肿瘤切除后,患者的症状得到了缓解。
手术切除后症状的缓解表明,这些症状可能与肿瘤的占位效应有关,或者是由于儿茶酚胺水平升高的非典型表现。此外,通过筛查嗜铬细胞瘤,患者能够避免常见的胃肠诊断程序可能导致的潜在并发症。该病例报告强调了在面对可能是非特异性或与周围器官占位效应相关的症状时,筛查嗜铬细胞瘤的潜在益处。