{"title":"Giant symptomatic myelolipoma of the right adrenal gland: a case report.","authors":"Roberto Dell'Avanzato, Fabio Castaldi, Cristiano Giovannini, Edoardo Mercadante, Paolo Cianciulli, Massimo Carlini","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Adrenal myelolipoma is an uncommon tumour of the adrenal gland, usually unilateral, frequently associated with hypertension and obesity, with a benign biological behaviour and without hormonal activity, first described in 1905. The neoplasm consists of adipose tissue and myelopoietic cells of the bone marrow. These tumours have a very slow but continued growth and their volume and weight vary significantly from small lesions of a few grams to huge masses weighing up to several kilograms. If symptoms occur, surgery should be performed without delay, especially for large myelolipomas that are at high risk of spontaneous rupture with haemorrhage and life-threatening shock. In this report a case of a 43-year-old male with a 22 x 18 x 9 cm giant myelolipoma, weighing 3500 g and originating from the right adrenal gland is described. The large mass dislocating and compressing the inferior vena cava, was removed surgically. The early postoperative course and the late outcome were favourable without recurrence after 30 months. The different aetiological hypotheses of this rare neoplasm and its clinical features, diagnosis and treatment are discussed.</p>","PeriodicalId":75700,"journal":{"name":"Chirurgia italiana","volume":"61 2","pages":"231-6"},"PeriodicalIF":0.0000,"publicationDate":"2009-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chirurgia italiana","FirstCategoryId":"1085","ListUrlMain":"","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
Adrenal myelolipoma is an uncommon tumour of the adrenal gland, usually unilateral, frequently associated with hypertension and obesity, with a benign biological behaviour and without hormonal activity, first described in 1905. The neoplasm consists of adipose tissue and myelopoietic cells of the bone marrow. These tumours have a very slow but continued growth and their volume and weight vary significantly from small lesions of a few grams to huge masses weighing up to several kilograms. If symptoms occur, surgery should be performed without delay, especially for large myelolipomas that are at high risk of spontaneous rupture with haemorrhage and life-threatening shock. In this report a case of a 43-year-old male with a 22 x 18 x 9 cm giant myelolipoma, weighing 3500 g and originating from the right adrenal gland is described. The large mass dislocating and compressing the inferior vena cava, was removed surgically. The early postoperative course and the late outcome were favourable without recurrence after 30 months. The different aetiological hypotheses of this rare neoplasm and its clinical features, diagnosis and treatment are discussed.
肾上腺骨髓瘤是一种罕见的肾上腺肿瘤,通常为单侧,常与高血压和肥胖相关,具有良性生物学行为,无激素活性,于1905年首次被描述。肿瘤由脂肪组织和骨髓的骨髓生成细胞组成。这些肿瘤生长缓慢但持续,其体积和重量变化很大,小到几克,大到几公斤。如果出现症状,应立即进行手术治疗,特别是对于有自发性破裂并出血和危及生命的休克高风险的大骨髓瘤。在这个报告中,我们描述了一个43岁男性,患有22 x 18 x 9厘米的巨大骨髓脂肪瘤,重3500克,起源于右肾上腺。大肿块脱位和压迫下腔静脉,手术切除。术后早期和晚期预后良好,30个月后无复发。本文讨论了这种罕见肿瘤的不同病因假说及其临床特征、诊断和治疗。