Adas Mine, Koc Bora, Adas Gokhan, Ozulker Filiz, Aydin Tamer
Department of Surgery, Okmeydani Training and Research Hospital, 34200 Şişli, İstanbul, Turkey.
J Med Case Rep. 2014 Apr 29;8:131. doi: 10.1186/1752-1947-8-131.
Ganglioneuromas are rare benign tumors arising from the neural crest tissue and are most commonly located in the posterior mediastinum and retroperitoneum; they are rarely found in the adrenal gland. This tumor is usually asymptomatic and in the majority of cases is detected incidentally. Although the characteristics of adrenal ganglioneuroma on computerized tomography and magnetic resonance imaging have been well described, the exact diagnosis is difficult. Histopathological examination is currently the mainstay of diagnosis. Ganglioneuromas have a very good prognosis with surgical removal. We report the case of a male patient with an incidentally identified adrenal ganglioneuroma with high standardized uptake values in a positron emission tomography scan.
An 18-year-old Turkish male patient with no previous comorbidities was admitted to our hospital with lower-quadrant pain. He had no significant past medical or surgical history. A physical examination did not reveal any signs and the results of routine laboratory tests were all within the normal ranges. Our patient underwent computed tomography of his abdomen, which showed a relatively homogenous left adrenal tumor measuring 5.2 × 4.3 × 7.1cm. On a positron emission tomography scan, the left adrenal gland disclosed a standardized uptake value of 4.1. Our patient underwent an exploratory laparotomy with left adrenalectomy without any related complications.
Ganglioneuroma may sometimes be similar to other adrenal malignancies. Careful evaluation with endocrine tests and imaging procedures is necessary to provide an accurate diagnosis. Definitive diagnosis can be made by histological examination. The prognosis is very good with surgical removal.
神经节神经瘤是一种罕见的起源于神经嵴组织的良性肿瘤,最常见于后纵隔和腹膜后;肾上腺中很少见。这种肿瘤通常无症状,大多数情况下是偶然发现的。虽然肾上腺神经节神经瘤在计算机断层扫描和磁共振成像上的特征已有详细描述,但准确诊断仍很困难。组织病理学检查是目前诊断的主要依据。手术切除后神经节神经瘤的预后非常好。我们报告一例男性患者,偶然发现肾上腺神经节神经瘤,在正电子发射断层扫描中标准化摄取值较高。
一名18岁无既往合并症的土耳其男性患者因下腹部疼痛入院。他既往无重大病史或手术史。体格检查未发现任何体征,常规实验室检查结果均在正常范围内。患者接受了腹部计算机断层扫描,显示左肾上腺有一个相对均匀的肿瘤,大小为5.2×4.3×7.1cm。在正电子发射断层扫描中,左肾上腺的标准化摄取值为4.1。患者接受了剖腹探查术及左肾上腺切除术,未出现任何相关并发症。
神经节神经瘤有时可能与其他肾上腺恶性肿瘤相似。需要通过内分泌检查和影像学检查进行仔细评估以做出准确诊断。最终诊断可通过组织学检查确定。手术切除后预后非常好。