Kelvin Candiago, E. Manuputty, Syamsu Hudaya, Yulius Fajar Martanu, Budiawan Atmadja, A. Harahap, Yosephine G Susufi, Yustinus Hartanto, Ajeng Indah Pramesti
{"title":"Laparoscopic Approach in Large Rare Adrenal Ganglioneuroma","authors":"Kelvin Candiago, E. Manuputty, Syamsu Hudaya, Yulius Fajar Martanu, Budiawan Atmadja, A. Harahap, Yosephine G Susufi, Yustinus Hartanto, Ajeng Indah Pramesti","doi":"10.33371/ijoc.v16i3.889","DOIUrl":null,"url":null,"abstract":"Introduction: Adrenal ganglioneuroma is an extremely rare and benign tumor comprising Schwann cells and ganglion cells. Adrenal ganglioneuroma is usually hormonally silent and tends to be discovered incidentally on imaging tests. Here, we present a case of a 39-year-old man with adrenal ganglioneuroma who underwent laparoscopic left adrenalectomy.Case Presentation: a 39-year-old man was admitted to our department with left flank pain after he recovered from Covid-19. He had no symptoms of nausea, vomiting, headache, diarrhea, palpitation, or chest distress, and there was no lack of appetite or weight loss. He denied any medical conditions, such as hyperaldosteronism, hypercortisolism, and hypertension. On further examination with contrast-enhanced CT identified a hypo-isodense mass in the left adrenal gland, measuring 4.8 x 4.4 x 5.0 cm, and spotty dense calcification in the middle of the mass. All functional laboratory evolution showed negative including urinalysis and serum electrolyte. Because the non-functioning suprarenal tumor was presumed to be benign, a laparoscopic approach was planned for definitive extirpation of the left adrenal gland. CT triple-phase whole abdomen was done before the procedure which showed contrast-enhanced identified an isodense mass with 43 HU in the left adrenal gland, measuring 4.8 x 4.4 x 5.0 cm with absolute washout of 49.3% and relative washout of 30.7%. Laparoscopic left adrenalectomy was performed. The patient underwent successful laparoscopic extirpation of the left adrenal gland. The postoperative pathology revealed a 7.0 x 6.0 x 3.0 cm encapsulated tumor with a firm texture. Microscopically, the tumor showed a mixture of mature ganglion cells and fascicles of Schwann cells. Adrenocortical cells were found near the capsule.Conclusions: Even though there have been some guidelines for the diagnosis of Adrenal ganglioneuroma, pre-operative misdiagnoses are still frequent. We recommend that complete operative resection should be considered once malignancy cannot be excluded by pre-operative evaluation. Laparoscopic adrenalectomy is a reasonable option at least for tumors < or = 4.5 cm. Adrenal ganglioneuroma can be successfully excised laparoscopically with an appropriate and experienced surgeon.","PeriodicalId":13489,"journal":{"name":"Indonesian Journal of Cancer","volume":"31 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indonesian Journal of Cancer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.33371/ijoc.v16i3.889","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Adrenal ganglioneuroma is an extremely rare and benign tumor comprising Schwann cells and ganglion cells. Adrenal ganglioneuroma is usually hormonally silent and tends to be discovered incidentally on imaging tests. Here, we present a case of a 39-year-old man with adrenal ganglioneuroma who underwent laparoscopic left adrenalectomy.Case Presentation: a 39-year-old man was admitted to our department with left flank pain after he recovered from Covid-19. He had no symptoms of nausea, vomiting, headache, diarrhea, palpitation, or chest distress, and there was no lack of appetite or weight loss. He denied any medical conditions, such as hyperaldosteronism, hypercortisolism, and hypertension. On further examination with contrast-enhanced CT identified a hypo-isodense mass in the left adrenal gland, measuring 4.8 x 4.4 x 5.0 cm, and spotty dense calcification in the middle of the mass. All functional laboratory evolution showed negative including urinalysis and serum electrolyte. Because the non-functioning suprarenal tumor was presumed to be benign, a laparoscopic approach was planned for definitive extirpation of the left adrenal gland. CT triple-phase whole abdomen was done before the procedure which showed contrast-enhanced identified an isodense mass with 43 HU in the left adrenal gland, measuring 4.8 x 4.4 x 5.0 cm with absolute washout of 49.3% and relative washout of 30.7%. Laparoscopic left adrenalectomy was performed. The patient underwent successful laparoscopic extirpation of the left adrenal gland. The postoperative pathology revealed a 7.0 x 6.0 x 3.0 cm encapsulated tumor with a firm texture. Microscopically, the tumor showed a mixture of mature ganglion cells and fascicles of Schwann cells. Adrenocortical cells were found near the capsule.Conclusions: Even though there have been some guidelines for the diagnosis of Adrenal ganglioneuroma, pre-operative misdiagnoses are still frequent. We recommend that complete operative resection should be considered once malignancy cannot be excluded by pre-operative evaluation. Laparoscopic adrenalectomy is a reasonable option at least for tumors < or = 4.5 cm. Adrenal ganglioneuroma can be successfully excised laparoscopically with an appropriate and experienced surgeon.
简介:肾上腺神经节神经瘤是一种由雪旺细胞和神经节细胞组成的极为罕见的良性肿瘤。肾上腺神经节神经瘤通常无激素表现,往往在影像学检查中偶然发现。在此,我们报告一个39岁男性肾上腺神经节神经瘤的病例,他接受了腹腔镜左肾上腺切除术。病例介绍:一名39岁男性,新冠肺炎康复后因左侧疼痛入院。他没有恶心、呕吐、头痛、腹泻、心悸或胸闷的症状,也没有食欲不振或体重减轻。他否认有任何疾病,如醛固酮增多症、高皮质醇血症和高血压。进一步CT增强检查发现左侧肾上腺低等密度肿块,尺寸为4.8 x 4.4 x 5.0 cm,肿块中部有点状致密钙化。所有功能实验室检测结果均为阴性,包括尿液和血清电解质。由于无功能的肾上肿瘤被认为是良性的,因此计划采用腹腔镜方法切除左侧肾上腺。术前行全腹CT三期增强扫描,左侧肾上腺见43 HU等致密肿块,尺寸4.8 x 4.4 x 5.0 cm,绝对洗脱率49.3%,相对洗脱率30.7%。行腹腔镜左肾上腺切除术。病人接受了成功的腹腔镜左肾上腺摘除手术。术后病理显示一个7.0 x 6.0 x 3.0 cm的包膜肿瘤,质地坚硬。显微镜下,肿瘤显示成熟神经节细胞和雪旺细胞束的混合物。被膜附近可见肾上腺皮质细胞。结论:尽管有一些肾上腺神经节神经瘤的诊断指南,但术前误诊仍然很常见。我们建议,一旦术前评估不能排除恶性肿瘤,应考虑完全手术切除。至少对于小于或= 4.5 cm的肿瘤,腹腔镜肾上腺切除术是一个合理的选择。肾上腺神经节神经瘤可以成功切除腹腔镜与适当的和有经验的外科医生。