Giant adrenal myelolipoma is a rare, benign, sizable, mesenchymal tumor. Preoperative differential diagnosis from retroperitoneal liposarcoma may be challenging. A 66-year-old female patient was admitted because of a sizable tumor at the right retroperitoneal space, incidentally discovered during abdominal ultrasonography for screening purpose. Preoperative imaging studies were indicative for the diagnosis of a giant adrenal myelolipoma (11.7 × 12.9 cm in size); however, a retroperitoneal liposarcoma could not be excluded. We decided to proceed with tumor's surgical removal by using laparoscopic transperitoneal approach and three-dimensional high-definition camera. Intraoperatively, the tumor did not infiltrate surrounding tissues and was surrounded by a thin capsule under which there were sparse, orange-colored spots that resembled adrenal cortex. This finding reinforced the initial and most possible diagnosis of adrenal myelolipoma and we easily enucleated the mass. Postoperative course was uneventful, and the patient demonstrated no recurrence on imaging six months postoperatively. Histology confirmed the diagnosis of giant adrenal myelolipoma, measuring 16.5 x 15 x 6.5 cm.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001128PMC
http://dx.doi.org/10.7759/cureus.6582DOI Listing

Publication Analysis

Top Keywords

adrenal myelolipoma
20
giant adrenal
16
diagnosis giant
12
differential diagnosis
8
retroperitoneal liposarcoma
8
adrenal
6
myelolipoma
5
diagnosis
5
macroscopic appearance
4
giant
4

Similar Publications

Introduction: Adrenal myelolipomas are uncommon benign adrenal tumors, which mostly occur unilaterally. We describe a rare case of giant bilateral adrenal myelolipoma mistaken for retroperitoneal liposarcoma.

Case Presentation: A 49-year-old man developed fever, left flank pain, and a large mass in his left abdomen.

View Article and Find Full Text PDF

Objective: Isolated adrenal myelolipoma (IAM) is an uncommon, nonfunctioning tumour of the adrenal gland, primarily composed of adipose tissue and hematopoietic trilinear cells. The etiopathogenesis and clinical relevance of this neoplasm remain poorly understood. However, similar myelolipomatous alterations can also occur within adrenocortical adenomas.

View Article and Find Full Text PDF

Laparoscopic resection of giant adrenal myelolipoma: A case report with review of literature.

Radiol Case Rep

November 2024

Smart Health Tower, Madam Mitterrand Street, Sulaymaniyah, Kurdistan, Iraq.

Giant adrenal myelolipoma (AML) may cause severe symptoms. In contrast to the previous reports, laparoscopy may play a pivotal role in the management of giant AML. This report aims to discuss a case of giant AML managed successfully by laparoscopy.

View Article and Find Full Text PDF
Article Synopsis
  • Pheochromocytomas are rare adrenal tumors that can cause various symptoms, potentially leading to misdiagnosis and serious complications, such as hypertensive crises and cardiovascular damage from chronic high blood pressure.
  • A case of a 45-year-old woman with gastrointestinal symptoms was found to be related to a pheochromocytoma, confirmed through biochemical testing before undergoing any procedures that could provoke dangerous surges of catecholamines.
  • The patient's symptoms resolved after surgical removal of the tumor, illustrating the importance of screening for pheochromocytoma in individuals presenting with non-specific symptoms that might impact surrounding organs.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!