A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin

Adrenal incidentalomas (AIs) are mostly benign and nonsecretory. Management algorithms lack sensitivity when assessing malignant potential, although functional status is easier to assess. We present a subject whose AI was a retroperitoneal leiomyosarcoma (RL). Case Presentation. A woman on warfarin...

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Main Authors: Ishrat N. Khan, Mohamed A. Adlan, Michael J. Stechman, Lakdasa D. Premawardhana
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Case Reports in Endocrinology
Online Access:http://dx.doi.org/10.1155/2015/830814
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author Ishrat N. Khan
Mohamed A. Adlan
Michael J. Stechman
Lakdasa D. Premawardhana
author_facet Ishrat N. Khan
Mohamed A. Adlan
Michael J. Stechman
Lakdasa D. Premawardhana
author_sort Ishrat N. Khan
collection DOAJ
description Adrenal incidentalomas (AIs) are mostly benign and nonsecretory. Management algorithms lack sensitivity when assessing malignant potential, although functional status is easier to assess. We present a subject whose AI was a retroperitoneal leiomyosarcoma (RL). Case Presentation. A woman on warfarin with SLE and the antiphospholipid syndrome, presented with left loin pain. She was normotensive and clinically normal. Ultrasound scans demonstrated left kidney scarring, but CT scans revealed an AI. MRI scans later confirmed the AI without significant fat and no interval growth. Cortisol after 1 mg dexamethasone, urinary free cortisol and catecholamines, plasma aldosterone renin ratio, and 17-hydroxyprogesterone were within the reference range. Initially, adrenal haemorrhage was diagnosed because of warfarin therapy and the acute presentation. However, she underwent adrenalectomy because of interval growth of the AI. Histology confirmed an RL. The patient received adjuvant radiotherapy. Discussion. Our subject presented with an NSAI. However, we highlight the following: (a) the diagnosis of adrenal haemorrhage in this anticoagulated woman was revised because of interval growth; (b) the tumour, an RL, was relatively small at diagnosis; (c) this subject has survived well over 60 months despite an RL perhaps because of her acute presentation and early diagnosis of a small localised tumour.
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spelling doaj-art-e70f6d372b2b4479a13b820d151d8ee82025-02-03T01:00:10ZengWileyCase Reports in Endocrinology2090-65012090-651X2015-01-01201510.1155/2015/830814830814A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on WarfarinIshrat N. Khan0Mohamed A. Adlan1Michael J. Stechman2Lakdasa D. Premawardhana3Section of Endocrinology, Ysbyty Ystrad Fawr, Ystrad Fawr Way, Hengoed, Caerphilly CF82 7EP, UKSection of Endocrinology, Ysbyty Ystrad Fawr, Ystrad Fawr Way, Hengoed, Caerphilly CF82 7EP, UKDepartment of Endocrine Surgery, University Hospital of Wales, Heath Park, Cardiff CF14 4XN, UKSection of Endocrinology, Ysbyty Ystrad Fawr, Ystrad Fawr Way, Hengoed, Caerphilly CF82 7EP, UKAdrenal incidentalomas (AIs) are mostly benign and nonsecretory. Management algorithms lack sensitivity when assessing malignant potential, although functional status is easier to assess. We present a subject whose AI was a retroperitoneal leiomyosarcoma (RL). Case Presentation. A woman on warfarin with SLE and the antiphospholipid syndrome, presented with left loin pain. She was normotensive and clinically normal. Ultrasound scans demonstrated left kidney scarring, but CT scans revealed an AI. MRI scans later confirmed the AI without significant fat and no interval growth. Cortisol after 1 mg dexamethasone, urinary free cortisol and catecholamines, plasma aldosterone renin ratio, and 17-hydroxyprogesterone were within the reference range. Initially, adrenal haemorrhage was diagnosed because of warfarin therapy and the acute presentation. However, she underwent adrenalectomy because of interval growth of the AI. Histology confirmed an RL. The patient received adjuvant radiotherapy. Discussion. Our subject presented with an NSAI. However, we highlight the following: (a) the diagnosis of adrenal haemorrhage in this anticoagulated woman was revised because of interval growth; (b) the tumour, an RL, was relatively small at diagnosis; (c) this subject has survived well over 60 months despite an RL perhaps because of her acute presentation and early diagnosis of a small localised tumour.http://dx.doi.org/10.1155/2015/830814
spellingShingle Ishrat N. Khan
Mohamed A. Adlan
Michael J. Stechman
Lakdasa D. Premawardhana
A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin
Case Reports in Endocrinology
title A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin
title_full A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin
title_fullStr A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin
title_full_unstemmed A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin
title_short A Retroperitoneal Leiomyosarcoma Presenting as an Adrenal Incidentaloma in a Subject on Warfarin
title_sort retroperitoneal leiomyosarcoma presenting as an adrenal incidentaloma in a subject on warfarin
url http://dx.doi.org/10.1155/2015/830814
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