Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature

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 ima...

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Main Authors: Junaid Nabi, Danish Rafiq, Fatema N. Authoy, Ghulam Nabi Sofi
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:Case Reports in Urology
Online Access:http://dx.doi.org/10.1155/2013/789481
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author Junaid Nabi
Danish Rafiq
Fatema N. Authoy
Ghulam Nabi Sofi
author_facet Junaid Nabi
Danish Rafiq
Fatema N. Authoy
Ghulam Nabi Sofi
author_sort Junaid Nabi
collection DOAJ
description 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.
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spelling doaj-art-bf552c7462264bb1b2f1a2dc116ebbbb2025-02-03T05:46:10ZengWileyCase Reports in Urology2090-696X2090-69782013-01-01201310.1155/2013/789481789481Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of LiteratureJunaid Nabi0Danish Rafiq1Fatema N. Authoy2Ghulam Nabi Sofi3Department of Surgery, Shaheed Suhrawardy Medical College and Hospital, Dhaka 1207, BangladeshDepartment of Pathology, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, IndiaDepartment of Surgery, Shaheed Suhrawardy Medical College and Hospital, Dhaka 1207, BangladeshDepartment of Pathology, Sher-I-Kashmir Institute of Medical Sciences, Srinagar, Jammu and Kashmir, IndiaIntroduction. 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.http://dx.doi.org/10.1155/2013/789481
spellingShingle Junaid Nabi
Danish Rafiq
Fatema N. Authoy
Ghulam Nabi Sofi
Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature
Case Reports in Urology
title Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature
title_full Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature
title_fullStr Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature
title_full_unstemmed Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature
title_short Incidental Detection of Adrenal Myelolipoma: A Case Report and Review of Literature
title_sort incidental detection of adrenal myelolipoma a case report and review of literature
url http://dx.doi.org/10.1155/2013/789481
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AT fatemanauthoy incidentaldetectionofadrenalmyelolipomaacasereportandreviewofliterature
AT ghulamnabisofi incidentaldetectionofadrenalmyelolipomaacasereportandreviewofliterature