Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2013:2013:789481.
doi: 10.1155/2013/789481. Epub 2013 Feb 20.

Incidental detection of adrenal myelolipoma: a case report and review of literature

Affiliations

Incidental detection of adrenal myelolipoma: a case report and review of literature

Junaid Nabi et al. Case Rep Urol. 2013.

Abstract

Introduction. Adrenal myelolipoma is a rare tumor that is benign in nature, usually asymptomatic, unilateral, and nonsecreting. It is composed of variable mixture of mature adipose tissue and hematopoietic elements and develops within the adrenal gland. With the widespread use of cross-sectional imaging modalities such as ultrasonography and computed tomography, the incidental detection of these tumors is increasing in frequency. Case Presentation. We report a case of adrenal myelolipoma in a 63-year-old Kashmiri male, who presented with pain in the right upper abdomen. Physical examination was unremarkable. Ultrasound abdomen showed the presence of a hyperechoic mass in the right suprarenal region with undefined margins. Contrast-enhanced computed tomography (CECT) scan of abdomen revealed a well-defined, round lesion in the right suprarenal region with heterogeneous attenuation suggesting the possibility of myelolipoma. The patient was subjected to right adrenalectomy and his postoperative course was uneventful. The histopathological evaluation of the mass confirmed the initial diagnosis of adrenal myelolipoma. Conclusion. Although mostly discovered as an "incidentaloma", the diagnosis of adrenal myelolipoma warrants thorough diagnostic study. Imaging techniques such as ultrasonography and CT scans as well as biochemical studies are useful for indicating the best treatment taking into account the size of the mass and possible hormone production. Surgical resection is advocated through extraperitoneal approach as it minimizes postoperative complications and leads to quicker recovery.

PubMed Disclaimer

Figures

Figure 1
Figure 1
CT appearance of myelolipoma. Contrast-enhanced CT scan of the upper abdomen showing the heterogeneous mass covering upper right retroperitoneal space (arrows) with variable central and peripheral attenuation.
Figure 2
Figure 2
Cut surface of adrenal myelolipoma showing a variegated appearance of dark brown and yellowish areas.
Figure 3
Figure 3
Microscopic appearance of adrenal myelolipoma. Typical histological features of myelolipoma comprising varying proportions of adipose tissue admixed with areas of hematopoietic tissue (H&E stain, ×40).

References

    1. Ersoy E, Ozdoğan M, Demirağ A, et al. Giant adrenal myelolipoma associated with small bowel leiomyosarcoma: a case report. The Turkish Journal of Gastroenterology. 2006;17:126–129. - PubMed
    1. Daneshmand S, Quek ML. Adrenal myelolipoma: diagnosis and management. Journal of Urology. 2006;3:71–74. - PubMed
    1. Brogna A, Scalisi G, Ferrara R, Bucceri AM. Giant secreting adrenal myelolipoma in a man: a case report. Journal of Medical Case Reports. 2011;5, article 298 - PMC - PubMed
    1. Settakorn J, Sirivanichai C, Rangdaeng S, Chaiwun B. Fine-needle aspiration cytology of adrenal myelolipoma: case report and review of the literature. Diagnostic Cytopathology. 1999;21:409–412. - PubMed
    1. Porcaro AB, Novella G, Ficarra V, Cavalleri S, Antoniolli SZ, Curti P. Incidentally discovered adrenal myelolipoma. Report on 3 operated patients and update of the literature. Archivio Italiano di Urologia, Andrologia. 2002;74(3):146–151. - PubMed

LinkOut - more resources