Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case

Abstract Epithelioid sarcoma is a rare aggressive soft tissue sarcoma, which can be distal or proximal types. The classic form (distal-type) of epithelioid sarcoma mainly occurs in teenagers and young adults. A rarer form, called large-cell (proximal-type) epithelioid sarcoma, tends to be more aggressive and mainly affects adults. The proximal subtype mostly arises from the proximal pelvis, limbs, and genital tract. We report a case of a 59 -year-old female, presented with a progressively growing mass in the left labia majora. Gynecologic examination revealed a 2 cm mobile and painless mass that was not attached to deep planes. The histological study showed a multinodular tumor was seen comprising sheets of oval to polygonal cells with moderate amount of cytoplasm. Interspersed were larger, rhabdoid cells with abundant eosinophilic cytoplasm and prominent nucleoli. On IHC, the tumor cells showed positivity for EMA and CKAE1/AE3 and do not expressed INI-1 in the nucleus. All tumor cells were negative for S-100 protein and CD34. The histopathological diagnosis was soft tissue of the vulvar region with proximal epithelioid sarcoma. The patient received adjuvant external pelvic radiotherapy and brachytherapy in the vulvar bed. Currently, 3 years after diagnosis, the patient does not present signs of tumor recurrence in her controls. Due to its low incidence, there are no evidence-based diagnostic algorithms or published recommendations for treatment. The prognosis is generally poor. A wide excision with clear margins is imperative with options of post-operative CT/RT in individual cases during a close follow-upbehavior, as seen in our case.

Saved in:
Bibliographic Details
Main Authors: Sarabia-Ochoa,Rosalía, García-de la Torre,Juan Pablo, Amezcua-Recover,Antonio
Format: Digital revista
Language:English
Published: Hospital San Pedro 2024
Online Access:https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S2695-50752024000100004
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S2695-50752024000100004
record_format ojs
spelling oai:scielo:S2695-507520240001000042024-10-28Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological caseSarabia-Ochoa,RosalíaGarcía-de la Torre,Juan PabloAmezcua-Recover,Antonio Vulva Epithelioid sarcoma Proximal epithelioid sarcoma Abstract Epithelioid sarcoma is a rare aggressive soft tissue sarcoma, which can be distal or proximal types. The classic form (distal-type) of epithelioid sarcoma mainly occurs in teenagers and young adults. A rarer form, called large-cell (proximal-type) epithelioid sarcoma, tends to be more aggressive and mainly affects adults. The proximal subtype mostly arises from the proximal pelvis, limbs, and genital tract. We report a case of a 59 -year-old female, presented with a progressively growing mass in the left labia majora. Gynecologic examination revealed a 2 cm mobile and painless mass that was not attached to deep planes. The histological study showed a multinodular tumor was seen comprising sheets of oval to polygonal cells with moderate amount of cytoplasm. Interspersed were larger, rhabdoid cells with abundant eosinophilic cytoplasm and prominent nucleoli. On IHC, the tumor cells showed positivity for EMA and CKAE1/AE3 and do not expressed INI-1 in the nucleus. All tumor cells were negative for S-100 protein and CD34. The histopathological diagnosis was soft tissue of the vulvar region with proximal epithelioid sarcoma. The patient received adjuvant external pelvic radiotherapy and brachytherapy in the vulvar bed. Currently, 3 years after diagnosis, the patient does not present signs of tumor recurrence in her controls. Due to its low incidence, there are no evidence-based diagnostic algorithms or published recommendations for treatment. The prognosis is generally poor. A wide excision with clear margins is imperative with options of post-operative CT/RT in individual cases during a close follow-upbehavior, as seen in our case.Hospital San PedroIberoamerican Journal of Medicine v.6 n.1 20242024-01-01journal articletext/htmlhttps://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S2695-50752024000100004en
institution SCIELO
collection OJS
country España
countrycode ES
component Revista
access En linea
databasecode rev-scielo-es
tag revista
region Europa del Sur
libraryname SciELO
language English
format Digital
author Sarabia-Ochoa,Rosalía
García-de la Torre,Juan Pablo
Amezcua-Recover,Antonio
spellingShingle Sarabia-Ochoa,Rosalía
García-de la Torre,Juan Pablo
Amezcua-Recover,Antonio
Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case
author_facet Sarabia-Ochoa,Rosalía
García-de la Torre,Juan Pablo
Amezcua-Recover,Antonio
author_sort Sarabia-Ochoa,Rosalía
title Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case
title_short Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case
title_full Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case
title_fullStr Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case
title_full_unstemmed Proximal epithelioid sarcoma of the vulva. A rare neoplasm. A clinicopathological case
title_sort proximal epithelioid sarcoma of the vulva. a rare neoplasm. a clinicopathological case
description Abstract Epithelioid sarcoma is a rare aggressive soft tissue sarcoma, which can be distal or proximal types. The classic form (distal-type) of epithelioid sarcoma mainly occurs in teenagers and young adults. A rarer form, called large-cell (proximal-type) epithelioid sarcoma, tends to be more aggressive and mainly affects adults. The proximal subtype mostly arises from the proximal pelvis, limbs, and genital tract. We report a case of a 59 -year-old female, presented with a progressively growing mass in the left labia majora. Gynecologic examination revealed a 2 cm mobile and painless mass that was not attached to deep planes. The histological study showed a multinodular tumor was seen comprising sheets of oval to polygonal cells with moderate amount of cytoplasm. Interspersed were larger, rhabdoid cells with abundant eosinophilic cytoplasm and prominent nucleoli. On IHC, the tumor cells showed positivity for EMA and CKAE1/AE3 and do not expressed INI-1 in the nucleus. All tumor cells were negative for S-100 protein and CD34. The histopathological diagnosis was soft tissue of the vulvar region with proximal epithelioid sarcoma. The patient received adjuvant external pelvic radiotherapy and brachytherapy in the vulvar bed. Currently, 3 years after diagnosis, the patient does not present signs of tumor recurrence in her controls. Due to its low incidence, there are no evidence-based diagnostic algorithms or published recommendations for treatment. The prognosis is generally poor. A wide excision with clear margins is imperative with options of post-operative CT/RT in individual cases during a close follow-upbehavior, as seen in our case.
publisher Hospital San Pedro
publishDate 2024
url https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S2695-50752024000100004
work_keys_str_mv AT sarabiaochoarosalia proximalepithelioidsarcomaofthevulvaarareneoplasmaclinicopathologicalcase
AT garciadelatorrejuanpablo proximalepithelioidsarcomaofthevulvaarareneoplasmaclinicopathologicalcase
AT amezcuarecoverantonio proximalepithelioidsarcomaofthevulvaarareneoplasmaclinicopathologicalcase
_version_ 1816171858557403136