{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T15:28:57Z","timestamp":1787758137763,"version":"build-2784847793"},"reference-count":9,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2022,4]]},"abstract":"<jats:sec>\n                    <jats:title\/>\n                    <jats:p>Juvenile granulosa cell ovarian tumor is a rare cause ofpseudo-precociouspuberty. We report a case of a 6-year-old female with neurofibromatosis type 1 (NF1), associated with pseudo-precocious puberty (PPP). A thorough workup revealed a large multi-cystic right ovarian mass, which turned out to be a juvenile granulosa cell tumor (JGCT). This report documented a rare case of PPP caused by JGCT in a child with NF1. Verbal consent was taken from the family.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/aam.aam_93_20","type":"journal-article","created":{"date-parts":[[2022,7,6]],"date-time":"2022-07-06T00:27:39Z","timestamp":1657067259000},"page":"165-167","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":1,"title":["Ovarian Cell Tumor in a Child with Neurofibromatosis Type 1"],"prefix":"10.4103","volume":"21","author":[{"given":"Lujain Majdi","family":"Qutub","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abdulmoein Eid","family":"Al-Agha","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","reference":[{"key":"R1-12-20240831","doi-asserted-by":"crossref","first-page":"l6597","DOI":"10.1136\/bmj.l6597","article-title":"Precocious puberty","volume":"368","author":"Bradley","year":"2020","journal-title":"BMJ"},{"key":"R2-12-20240831","doi-asserted-by":"crossref","first-page":"2353","DOI":"10.1002\/ajmg.a.38308","article-title":"Growth hormone excess in children with neurofibromatosis Type-1 and optic glioma","volume":"173","author":"Cambiaso","year":"2017","journal-title":"Am J Med Genet A"},{"key":"R3-12-20240831","doi-asserted-by":"crossref","first-page":"87","DOI":"10.1016\/j.urology.2019.02.012","article-title":"A rare case of uterine torsion with juvenile granulosa cell tumor in the pediatric patient","volume":"128","author":"Mohapatra","year":"2019","journal-title":"Urology"},{"key":"R4-12-20240831","doi-asserted-by":"crossref","first-page":"77","DOI":"10.1016\/j.clinimag.2019.03.008","article-title":"Juvenile granulosa cell tumor associated with Maffucci syndrome in pregnancy: A case report","volume":"56","author":"Xu","year":"2019","journal-title":"Clin Imaging"},{"key":"R5-12-20240831","doi-asserted-by":"crossref","first-page":"138","DOI":"10.1016\/j.jpag.2016.09.008","article-title":"Juvenile granulosa cell tumor of the ovary: A clinicopathologic study","volume":"30","author":"Wu","year":"2017","journal-title":"J Pediatr Adolesc Gynecol"},{"key":"R6-12-20240831","doi-asserted-by":"crossref","first-page":"101273","DOI":"10.1016\/j.beem.2019.04.007","article-title":"Peripheral precocious puberty including congenital adrenal hyperplasia: Causes, consequences, management and outcomes","volume":"33","author":"Haddad","year":"2019","journal-title":"Best Pract Res Clin Endocrinol Metab"},{"key":"R7-12-20240831","doi-asserted-by":"crossref","first-page":"62","DOI":"10.1016\/j.bpobgyn.2017.11.004","article-title":"Disorders of puberty","volume":"48","author":"Sultan","year":"2018","journal-title":"Best Pract Res Clin Obstet Gynaecol"},{"key":"R8-12-20240831","doi-asserted-by":"crossref","first-page":"230","DOI":"10.1159\/000438895","article-title":"Treatment of peripheral precocious puberty","volume":"29","author":"Schoelwer","year":"2016","journal-title":"Endocr Dev"},{"key":"R10-12-20240831","doi-asserted-by":"crossref","first-page":"e20190660","DOI":"10.1542\/peds.2019-0660","article-title":"Health supervision for children with neurofibromatosis Type 1","volume":"143","author":"Miller","year":"2019","journal-title":"Pediatrics"}],"container-title":["Annals of African Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.ovid.com\/10.4103\/aam.aam_93_20","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,8,26]],"date-time":"2026-08-26T15:04:41Z","timestamp":1787756681000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.ovid.com\/10.4103\/aam.aam_93_20"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,4]]},"references-count":9,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2022]]}},"URL":"https:\/\/doi.org\/10.4103\/aam.aam_93_20","relation":{},"ISSN":["1596-3519"],"issn-type":[{"value":"1596-3519","type":"print"}],"subject":[],"published":{"date-parts":[[2022,4]]}}}