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Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement

INTRODUCTION AND IMPORTANCE: Cervical localization of uterine tumor resembling an ovarian sex cord tumor is very rare (UTROSCT) and this is the third case reported in the English literature. Given its rarity, the diagnosis is frequently challenging. Our aim was to discuss pathological characteristic...

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Autores principales: Sahraoui, Ghada, Sassi, Farah, Charfi, Lamia, Ltaief, Feriel, Doghri, Raoudha, Mrad, Karima
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382843/
https://www.ncbi.nlm.nih.gov/pubmed/37429207
http://dx.doi.org/10.1016/j.ijscr.2023.108477
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author Sahraoui, Ghada
Sassi, Farah
Charfi, Lamia
Ltaief, Feriel
Doghri, Raoudha
Mrad, Karima
author_facet Sahraoui, Ghada
Sassi, Farah
Charfi, Lamia
Ltaief, Feriel
Doghri, Raoudha
Mrad, Karima
author_sort Sahraoui, Ghada
collection PubMed
description INTRODUCTION AND IMPORTANCE: Cervical localization of uterine tumor resembling an ovarian sex cord tumor is very rare (UTROSCT) and this is the third case reported in the English literature. Given its rarity, the diagnosis is frequently challenging. Our aim was to discuss pathological characteristics and treatment choices of this rare disease happening in a rare location. CASE PRESENTATION: Our case interested a 19-year-old female patient who presented with a lower abdominal pain and irregular menstrual cycles for a duration of two months. Gynecological examination revealed a cervical firm mass. The patient underwent a cervical lumpectomy. Microscopically, the tumor had nested and trabecular/cord patterns. Tumor cells had abundant cytoplasm, ovoid and spindle-shaped nuclei with fine chromatin. Mitoses were < 1/10 HPFs. A delicate vascular network of small capillaries was noted. Immunohistochemical staining showed that tumor cells were positive for Calretinin, AE1/AE3, Desmin, progesteron receptors, SMA and h-caldesmon. Pathological examination concluded to an UTROSCT. CLINICAL DISCUSSION: UTROSC is a rare tumor with only two cases with cervical involvement reported so far. They have an indolent clinical history and thus require a more cautious and less invasive therapeutic decision. The diagnosis remains on the pathological examination. CONCLUSION: This case is original by its location and the age of presentation. Careful follow-up is necessary searching for local recurrence or metastasis.
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spelling pubmed-103828432023-07-30 Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement Sahraoui, Ghada Sassi, Farah Charfi, Lamia Ltaief, Feriel Doghri, Raoudha Mrad, Karima Int J Surg Case Rep Case Report INTRODUCTION AND IMPORTANCE: Cervical localization of uterine tumor resembling an ovarian sex cord tumor is very rare (UTROSCT) and this is the third case reported in the English literature. Given its rarity, the diagnosis is frequently challenging. Our aim was to discuss pathological characteristics and treatment choices of this rare disease happening in a rare location. CASE PRESENTATION: Our case interested a 19-year-old female patient who presented with a lower abdominal pain and irregular menstrual cycles for a duration of two months. Gynecological examination revealed a cervical firm mass. The patient underwent a cervical lumpectomy. Microscopically, the tumor had nested and trabecular/cord patterns. Tumor cells had abundant cytoplasm, ovoid and spindle-shaped nuclei with fine chromatin. Mitoses were < 1/10 HPFs. A delicate vascular network of small capillaries was noted. Immunohistochemical staining showed that tumor cells were positive for Calretinin, AE1/AE3, Desmin, progesteron receptors, SMA and h-caldesmon. Pathological examination concluded to an UTROSCT. CLINICAL DISCUSSION: UTROSC is a rare tumor with only two cases with cervical involvement reported so far. They have an indolent clinical history and thus require a more cautious and less invasive therapeutic decision. The diagnosis remains on the pathological examination. CONCLUSION: This case is original by its location and the age of presentation. Careful follow-up is necessary searching for local recurrence or metastasis. Elsevier 2023-07-07 /pmc/articles/PMC10382843/ /pubmed/37429207 http://dx.doi.org/10.1016/j.ijscr.2023.108477 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Case Report
Sahraoui, Ghada
Sassi, Farah
Charfi, Lamia
Ltaief, Feriel
Doghri, Raoudha
Mrad, Karima
Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement
title Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement
title_full Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement
title_fullStr Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement
title_full_unstemmed Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement
title_short Unusual presentation of uterine tumors resembling ovarian sex cord tumor: A rare case report of cervical involvement
title_sort unusual presentation of uterine tumors resembling ovarian sex cord tumor: a rare case report of cervical involvement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10382843/
https://www.ncbi.nlm.nih.gov/pubmed/37429207
http://dx.doi.org/10.1016/j.ijscr.2023.108477
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