Cargando…

Fortuitously detected primary ovarian carcinoid tumor: A case report

Carcinoid tumors, derived from the cells of the disseminated neuroendocrine system, are rare, slow-growing neuroendocrine neoplasms that display a relatively indolent disease course. The majority of carcinoids are found within the gastrointestinal tract and bronchopulmonary system. Primary ovarian c...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Hwa Yeon, Pak, Min Gyoung, Park, Jung-Woo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402998/
https://www.ncbi.nlm.nih.gov/pubmed/37543794
http://dx.doi.org/10.1097/MD.0000000000034391
_version_ 1785084965514379264
author Choi, Hwa Yeon
Pak, Min Gyoung
Park, Jung-Woo
author_facet Choi, Hwa Yeon
Pak, Min Gyoung
Park, Jung-Woo
author_sort Choi, Hwa Yeon
collection PubMed
description Carcinoid tumors, derived from the cells of the disseminated neuroendocrine system, are rare, slow-growing neuroendocrine neoplasms that display a relatively indolent disease course. The majority of carcinoids are found within the gastrointestinal tract and bronchopulmonary system. Primary ovarian carcinoids are rare and account for merely 1% of all carcinoid tumors. We describe our experience of a rare case of primary ovarian carcinoid, presenting as chronic constipation, with no other carcinoid symptoms such as flushing, diarrhea, and wheezing. PATIENT CONCERNS: A 51-year-old postmenopausal woman with chronic constipation visited the clinic for routine check-up of her preexisting uterine fibroids. She had undergone hemorrhoidectomy 3 years ago. Physical examination revealed a soft abdomen without direct or rebound tenderness. Transvaginal ultrasonography revealed two subserosal fibroids, which had increased in size compared with previous ultrasonographic findings. A 3 cm hyperechoic mass was also detected in the right ovary. Her blood and urine tests were unremarkable, with no ascites in the pelvic cavity. She had a normal CA-125 level of 5.5 units/mL. DIAGNOSIS, INTERVENTIONS, AND OUTCOMES: The patient underwent a robot-assisted hysterectomy and right salpingo-oophorectomy because of enlarging fibroids and the right ovarian mass. Subsequently, based on the pathological and immunohistochemical findings, she was diagnosed with a primary ovarian carcinoid. The mass consisted of the insular and trabecular types of tumor cells. It was positive for pan-cytokeratin and synaptophysin, and the Ki-67 proliferation index was less than 1%. A follow-up positron emission tomography-computed tomography revealed no distant metastasis. Six months postoperatively, the patient was doing well without any signs of recurrence. LESSONS: Primary ovarian carcinoids without teratoma components are rare. It is crucial to make an accurate diagnosis based on the immunohistochemical staining results. Diagnosis in the early stages of the disease are associated with a favorable prognosis, but regular follow-up is mandatory.
format Online
Article
Text
id pubmed-10402998
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Lippincott Williams & Wilkins
record_format MEDLINE/PubMed
spelling pubmed-104029982023-08-05 Fortuitously detected primary ovarian carcinoid tumor: A case report Choi, Hwa Yeon Pak, Min Gyoung Park, Jung-Woo Medicine (Baltimore) Research Article: Clinical Case Report Carcinoid tumors, derived from the cells of the disseminated neuroendocrine system, are rare, slow-growing neuroendocrine neoplasms that display a relatively indolent disease course. The majority of carcinoids are found within the gastrointestinal tract and bronchopulmonary system. Primary ovarian carcinoids are rare and account for merely 1% of all carcinoid tumors. We describe our experience of a rare case of primary ovarian carcinoid, presenting as chronic constipation, with no other carcinoid symptoms such as flushing, diarrhea, and wheezing. PATIENT CONCERNS: A 51-year-old postmenopausal woman with chronic constipation visited the clinic for routine check-up of her preexisting uterine fibroids. She had undergone hemorrhoidectomy 3 years ago. Physical examination revealed a soft abdomen without direct or rebound tenderness. Transvaginal ultrasonography revealed two subserosal fibroids, which had increased in size compared with previous ultrasonographic findings. A 3 cm hyperechoic mass was also detected in the right ovary. Her blood and urine tests were unremarkable, with no ascites in the pelvic cavity. She had a normal CA-125 level of 5.5 units/mL. DIAGNOSIS, INTERVENTIONS, AND OUTCOMES: The patient underwent a robot-assisted hysterectomy and right salpingo-oophorectomy because of enlarging fibroids and the right ovarian mass. Subsequently, based on the pathological and immunohistochemical findings, she was diagnosed with a primary ovarian carcinoid. The mass consisted of the insular and trabecular types of tumor cells. It was positive for pan-cytokeratin and synaptophysin, and the Ki-67 proliferation index was less than 1%. A follow-up positron emission tomography-computed tomography revealed no distant metastasis. Six months postoperatively, the patient was doing well without any signs of recurrence. LESSONS: Primary ovarian carcinoids without teratoma components are rare. It is crucial to make an accurate diagnosis based on the immunohistochemical staining results. Diagnosis in the early stages of the disease are associated with a favorable prognosis, but regular follow-up is mandatory. Lippincott Williams & Wilkins 2023-08-04 /pmc/articles/PMC10402998/ /pubmed/37543794 http://dx.doi.org/10.1097/MD.0000000000034391 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.
spellingShingle Research Article: Clinical Case Report
Choi, Hwa Yeon
Pak, Min Gyoung
Park, Jung-Woo
Fortuitously detected primary ovarian carcinoid tumor: A case report
title Fortuitously detected primary ovarian carcinoid tumor: A case report
title_full Fortuitously detected primary ovarian carcinoid tumor: A case report
title_fullStr Fortuitously detected primary ovarian carcinoid tumor: A case report
title_full_unstemmed Fortuitously detected primary ovarian carcinoid tumor: A case report
title_short Fortuitously detected primary ovarian carcinoid tumor: A case report
title_sort fortuitously detected primary ovarian carcinoid tumor: a case report
topic Research Article: Clinical Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402998/
https://www.ncbi.nlm.nih.gov/pubmed/37543794
http://dx.doi.org/10.1097/MD.0000000000034391
work_keys_str_mv AT choihwayeon fortuitouslydetectedprimaryovariancarcinoidtumoracasereport
AT pakmingyoung fortuitouslydetectedprimaryovariancarcinoidtumoracasereport
AT parkjungwoo fortuitouslydetectedprimaryovariancarcinoidtumoracasereport