Hormone secreting juvenile granulosa cell tumor of the ovary in an infant presenting with massive ascites and precocious pseudopuberty

Autor: Minakshi Bhosale, Jyoti Kudrimoti, Deepak Dangmali

Publikováno v: CHRISMED Journal of Health and Research, Vol 8, Iss 2, Pp 136-138 (2021)

Juvenile granulosa cell tumors (JGCTs), account for 4–5% of GCTs, the rare sex cord stromal tumors. Presentation of JGCTs in infants is even rarer. We present case of a 3-month-old female infant with abdominal distension, feeding intolerance and fe

Externí odkaz: https://doaj.org/article/9f7b1fc2f5674bc2a2e78a7287ea3bbb

True precocious puberty following treatment of a Leydig cell tumour: two case reports and literature review

Autor: Alberto eVerrotti, Laura ePenta, Letizia eZenzeri, Laura eLucchetti, Paolo eGiovenali, Pierpaolo eDe Feo

Publikováno v: Frontiers in Pediatrics, Vol 3 (2015)

Leydig cell testicular tumours are a rare cause of precocious pseudopuberty in boys. Surgery is the main therapy and shows good overall prognosis. The physical signs of precocious puberty are expected to disappear shortly after surgical removal of th

Externí odkaz: https://doaj.org/article/0a571da4e66546b5aa410c9c253f5817

Precocious pseudopuberty due to virilising adrenocortical carcinoma progressing to central precocious puberty after surgery

Autor: Rajesh Khadgawat, Alpesh Goyal, Rakhi Malhotra

Publikováno v: BMJ Case Rep

A 7-year-old boy presented to our department with a 8-month history of progressive phallus enlargement and premature appearance of pubic and axillary hair. Parents also noticed increased irritability and aggressive behaviour in the child during this

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2639331aed35a33645ecf32e9254467
https://europepmc.org/articles/PMC6441251/

PRECOCIOUS PUBERTY DUE TO OVARIAN CYST – CASE REPORT

Autor: Guimarães, T.M., Tavares, M., Oliveira, M.J., Sousa, L., Borges, T.

Publikováno v: NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; Vol 22 No 2 (2013); 92-94
NASCER E CRESCER-BIRTH AND GROWTH MEDICAL JOURNAL; vol. 22 n.º 2 (2013); 92-94
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP

Introdução: Os quistos do ovário são raros na criança pré-púbere, representando os quistos funcionantes 5% dos casos. A manifestação clínica mais comum é o desenvolvimento de puberdade precoce isossexual. Caso clínico: Rapariga de cinco a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d865b451b74df169edde6bfa6c35499
https://revistas.rcaap.pt/nascercrescer/article/view/10767

Rare virilizing granulosa cell tumor in an adolescent

Autor: Gyöngyi Nagy, György Vajda, Dorottya Bús, Mária Buzogány

Publikováno v: Molecular and clinical oncology. 6(1)

Hormone-producing malignancies are rare in children or adolescent patients: Only 0.1% of all ovarian tumors and 4-5% of granulosa cell tumors occur in the sexually non-active ages. Granulosa cell tumors (GCTs) are sex cord-stromal tumors of the ovary

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29c98d6ed9355ec5c8e858b61557cb61
https://pubmed.ncbi.nlm.nih.gov/28123736