Primary retroperitoneal mullerian adenocarcinoma

Mullerian tumors are extremely rare malignancies in the retroperitoneum. We report a case of a 46-year old woman who presented with an eight year history of lower abdominal mass. Ultrasonography (US) and computed tomography (CT) demonstrated a 15×10 cm cystic mass in the left lower retroperitoneum....

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Main Authors: Ayman Elnemr, Yutaka Yonemura, Masaya Shinbo, Eisei Nishino
Format: Article
Language:English
Published: SAGE Publishing 2010-03-01
Series:Rare Tumors
Online Access:https://doi.org/10.4081/rt.2010.e6
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spelling doaj-ca5260f645164ce6a28c53d2b8522fe12020-11-25T03:35:51ZengSAGE PublishingRare Tumors2036-36132010-03-01210.4081/rt.2010.e6Primary retroperitoneal mullerian adenocarcinomaAyman Elnemr0Yutaka Yonemura1Masaya Shinbo2Eisei Nishino3Department of Surgery, Faculty of Medicine, Tanta University, EgyptNPO Organization to Support Peritoneal Surface Malignancy Treatment, Japan;NPO Organization to Support Peritoneal Surface Malignancy Treatment, Japan;Department of Pathology, Kishiwada Tokushukai Hospital, Kishiwada, Osaka, Japan;Mullerian tumors are extremely rare malignancies in the retroperitoneum. We report a case of a 46-year old woman who presented with an eight year history of lower abdominal mass. Ultrasonography (US) and computed tomography (CT) demonstrated a 15×10 cm cystic mass in the left lower retroperitoneum. As serial percutaneous needle aspiration cytology was negative for malignancy, she was observed for seven years. Eleven months ago, the mass was excised. The histopathology was reported as mucinous adenocarcinoma of the retroperitoneum. Six cycles of intraperitoneal (IP) chemotherapy was administered during the last six months after diagnosis of recurrence by aspiration cytology and high serum tumor markers (CEA, CA19-9). A few days ago, positron emission tomographic (PET) scanning showed evidence of local recurrence and single vertebral metastasis, so she was admitted again for systemic chemotherapy. Meticulous revision of additional sections of the tumor revealed papillary, serous, mucinous, and endometrioid subtypes of the mullerian adenocarcinoma. To our knowledge, there has been no similar case described in the literature.https://doi.org/10.4081/rt.2010.e6
collection DOAJ
language English
format Article
sources DOAJ
author Ayman Elnemr
Yutaka Yonemura
Masaya Shinbo
Eisei Nishino
spellingShingle Ayman Elnemr
Yutaka Yonemura
Masaya Shinbo
Eisei Nishino
Primary retroperitoneal mullerian adenocarcinoma
Rare Tumors
author_facet Ayman Elnemr
Yutaka Yonemura
Masaya Shinbo
Eisei Nishino
author_sort Ayman Elnemr
title Primary retroperitoneal mullerian adenocarcinoma
title_short Primary retroperitoneal mullerian adenocarcinoma
title_full Primary retroperitoneal mullerian adenocarcinoma
title_fullStr Primary retroperitoneal mullerian adenocarcinoma
title_full_unstemmed Primary retroperitoneal mullerian adenocarcinoma
title_sort primary retroperitoneal mullerian adenocarcinoma
publisher SAGE Publishing
series Rare Tumors
issn 2036-3613
publishDate 2010-03-01
description Mullerian tumors are extremely rare malignancies in the retroperitoneum. We report a case of a 46-year old woman who presented with an eight year history of lower abdominal mass. Ultrasonography (US) and computed tomography (CT) demonstrated a 15×10 cm cystic mass in the left lower retroperitoneum. As serial percutaneous needle aspiration cytology was negative for malignancy, she was observed for seven years. Eleven months ago, the mass was excised. The histopathology was reported as mucinous adenocarcinoma of the retroperitoneum. Six cycles of intraperitoneal (IP) chemotherapy was administered during the last six months after diagnosis of recurrence by aspiration cytology and high serum tumor markers (CEA, CA19-9). A few days ago, positron emission tomographic (PET) scanning showed evidence of local recurrence and single vertebral metastasis, so she was admitted again for systemic chemotherapy. Meticulous revision of additional sections of the tumor revealed papillary, serous, mucinous, and endometrioid subtypes of the mullerian adenocarcinoma. To our knowledge, there has been no similar case described in the literature.
url https://doi.org/10.4081/rt.2010.e6
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AT yutakayonemura primaryretroperitonealmullerianadenocarcinoma
AT masayashinbo primaryretroperitonealmullerianadenocarcinoma
AT eiseinishino primaryretroperitonealmullerianadenocarcinoma
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