An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review

In endometrial cancer (EC), adrenal metastases are rare indicating advanced disease. We report an unusual presentation of EC with solitary adrenal metastases at the time of diagnosis and provide with an updated literature review. A 68-year-old woman was referred with postmenopausal bleeding of sever...

Full description

Saved in:
Bibliographic Details
Main Authors: Maisie Ryan, Alexandros Laios, Darshana Pathak, Michael Weston, Richard Hutson
Format: Article
Language:English
Published: Wiley 2019-01-01
Series:Case Reports in Obstetrics and Gynecology
Online Access:http://dx.doi.org/10.1155/2019/3515869
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832562145481457664
author Maisie Ryan
Alexandros Laios
Darshana Pathak
Michael Weston
Richard Hutson
author_facet Maisie Ryan
Alexandros Laios
Darshana Pathak
Michael Weston
Richard Hutson
author_sort Maisie Ryan
collection DOAJ
description In endometrial cancer (EC), adrenal metastases are rare indicating advanced disease. We report an unusual presentation of EC with solitary adrenal metastases at the time of diagnosis and provide with an updated literature review. A 68-year-old woman was referred with postmenopausal bleeding of several weeks’ duration. Imaging revealed a heterogenous uterine mass and bilateral malignant adnexal masses. Hysteroscopy, endometrial biopsies, and radiological guided biopsies of the adrenal masses confirmed poorly differentiated EC. A PET-CT reported both adrenal metastases being hypermetabolic and suspicious for malignancy. The patient received six neoadjuvant chemotherapy cycles with Carboplatin and Paclitaxel. A repeated CT scan confirmed size reduction for both primary tumour and metastases. The adrenal metastases were no longer PET-avid on repeat PET-CT scan. The patient received a course of hormonal treatment and as per adrenal MDT, she underwent total laparoscopic hysterectomy and bilateral salpingo-oophorectomy followed by bilateral retroperitoneal laparoscopic adrenalectomy two months later. The patient remains asymptomatic on maintenance hydrocortisone 18 months post diagnosis. This is the first report of solitary synchronous adrenal metastases in a patient with EC. Central MDT review is key in providing individualised treatment recommendations of such rare entity.
format Article
id doaj-art-0680a7874e1b46f0aff3c25ed7de59c6
institution Kabale University
issn 2090-6684
2090-6692
language English
publishDate 2019-01-01
publisher Wiley
record_format Article
series Case Reports in Obstetrics and Gynecology
spelling doaj-art-0680a7874e1b46f0aff3c25ed7de59c62025-02-03T01:23:20ZengWileyCase Reports in Obstetrics and Gynecology2090-66842090-66922019-01-01201910.1155/2019/35158693515869An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature ReviewMaisie Ryan0Alexandros Laios1Darshana Pathak2Michael Weston3Richard Hutson4Department of Gynaecologic Oncology, St. James’s University Hospital, Leeds, UKDepartment of Gynaecologic Oncology, St. James’s University Hospital, Leeds, UKDepartment of Cellular Pathology, St. James’s University Hospital, Leeds, UKDapartment of Radiology, St. James’s University Hospital, Leeds, UKDepartment of Gynaecologic Oncology, St. James’s University Hospital, Leeds, UKIn endometrial cancer (EC), adrenal metastases are rare indicating advanced disease. We report an unusual presentation of EC with solitary adrenal metastases at the time of diagnosis and provide with an updated literature review. A 68-year-old woman was referred with postmenopausal bleeding of several weeks’ duration. Imaging revealed a heterogenous uterine mass and bilateral malignant adnexal masses. Hysteroscopy, endometrial biopsies, and radiological guided biopsies of the adrenal masses confirmed poorly differentiated EC. A PET-CT reported both adrenal metastases being hypermetabolic and suspicious for malignancy. The patient received six neoadjuvant chemotherapy cycles with Carboplatin and Paclitaxel. A repeated CT scan confirmed size reduction for both primary tumour and metastases. The adrenal metastases were no longer PET-avid on repeat PET-CT scan. The patient received a course of hormonal treatment and as per adrenal MDT, she underwent total laparoscopic hysterectomy and bilateral salpingo-oophorectomy followed by bilateral retroperitoneal laparoscopic adrenalectomy two months later. The patient remains asymptomatic on maintenance hydrocortisone 18 months post diagnosis. This is the first report of solitary synchronous adrenal metastases in a patient with EC. Central MDT review is key in providing individualised treatment recommendations of such rare entity.http://dx.doi.org/10.1155/2019/3515869
spellingShingle Maisie Ryan
Alexandros Laios
Darshana Pathak
Michael Weston
Richard Hutson
An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review
Case Reports in Obstetrics and Gynecology
title An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review
title_full An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review
title_fullStr An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review
title_full_unstemmed An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review
title_short An Unusual Presentation of Endometrial Cancer with Bilateral Adrenal Metastases at the Time of Presentation and an Updated Descriptive Literature Review
title_sort unusual presentation of endometrial cancer with bilateral adrenal metastases at the time of presentation and an updated descriptive literature review
url http://dx.doi.org/10.1155/2019/3515869
work_keys_str_mv AT maisieryan anunusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT alexandroslaios anunusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT darshanapathak anunusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT michaelweston anunusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT richardhutson anunusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT maisieryan unusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT alexandroslaios unusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT darshanapathak unusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT michaelweston unusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview
AT richardhutson unusualpresentationofendometrialcancerwithbilateraladrenalmetastasesatthetimeofpresentationandanupdateddescriptiveliteraturereview