A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature

Juvenile ovarian granulosa cell tumors (JGCTs) are described infrequently in pediatrics, and their finding in infants is exceptional. We highlight the presenting symptoms, radiologic images, operative management, and histopathologic findings of a 9-month-old female with isosexual pseudo-puberty. An...

Descripción completa

Detalles Bibliográficos
Autores principales: Ahmed, Shayma, Soliman, Ashraf, De Sanctis, Vincenzo, Alyafei, Fawzia, Alaaraj, Nada, Al Maadheed, Maryam, Clelland, Colin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mattioli 1885 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477099/
https://www.ncbi.nlm.nih.gov/pubmed/34487069
http://dx.doi.org/10.23750/abm.v92i4.11572
_version_ 1784575772459008000
author Ahmed, Shayma
Soliman, Ashraf
De Sanctis, Vincenzo
Alyafei, Fawzia
Alaaraj, Nada
Al Maadheed, Maryam
Clelland, Colin
author_facet Ahmed, Shayma
Soliman, Ashraf
De Sanctis, Vincenzo
Alyafei, Fawzia
Alaaraj, Nada
Al Maadheed, Maryam
Clelland, Colin
author_sort Ahmed, Shayma
collection PubMed
description Juvenile ovarian granulosa cell tumors (JGCTs) are described infrequently in pediatrics, and their finding in infants is exceptional. We highlight the presenting symptoms, radiologic images, operative management, and histopathologic findings of a 9-month-old female with isosexual pseudo-puberty. An updated revision of literature in infants below the age of 12 months is also reported. (www.actabiomedica.it)
format Online
Article
Text
id pubmed-8477099
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Mattioli 1885
record_format MEDLINE/PubMed
spelling pubmed-84770992021-10-08 A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature Ahmed, Shayma Soliman, Ashraf De Sanctis, Vincenzo Alyafei, Fawzia Alaaraj, Nada Al Maadheed, Maryam Clelland, Colin Acta Biomed Case Report Juvenile ovarian granulosa cell tumors (JGCTs) are described infrequently in pediatrics, and their finding in infants is exceptional. We highlight the presenting symptoms, radiologic images, operative management, and histopathologic findings of a 9-month-old female with isosexual pseudo-puberty. An updated revision of literature in infants below the age of 12 months is also reported. (www.actabiomedica.it) Mattioli 1885 2021 2021-09-02 /pmc/articles/PMC8477099/ /pubmed/34487069 http://dx.doi.org/10.23750/abm.v92i4.11572 Text en Copyright: © 2021 ACTA BIO MEDICA SOCIETY OF MEDICINE AND NATURAL SCIENCES OF PARMA https://creativecommons.org/licenses/by-nc-sa/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License
spellingShingle Case Report
Ahmed, Shayma
Soliman, Ashraf
De Sanctis, Vincenzo
Alyafei, Fawzia
Alaaraj, Nada
Al Maadheed, Maryam
Clelland, Colin
A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
title A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
title_full A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
title_fullStr A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
title_full_unstemmed A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
title_short A rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
title_sort rare case of ovarian juvenile granulosa cell tumor in an infant with isosexual pseudo puberty and revision of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477099/
https://www.ncbi.nlm.nih.gov/pubmed/34487069
http://dx.doi.org/10.23750/abm.v92i4.11572
work_keys_str_mv AT ahmedshayma ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT solimanashraf ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT desanctisvincenzo ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT alyafeifawzia ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT alaarajnada ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT almaadheedmaryam ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT clellandcolin ararecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT ahmedshayma rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT solimanashraf rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT desanctisvincenzo rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT alyafeifawzia rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT alaarajnada rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT almaadheedmaryam rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature
AT clellandcolin rarecaseofovarianjuvenilegranulosacelltumorinaninfantwithisosexualpseudopubertyandrevisionofliterature

Ejemplares similares