Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38665
Title: Leydig cell hyperplasia in children: Case series and review.
Authors: King S.K.;Marulaiah M.;Mennie N.;Ferguson P.;Heloury Y.;Kimber C.
Institution: (Mennie, Marulaiah, Ferguson, Kimber) Department of Paediatric Surgery, Monash Children's Hospital, Melbourne, Australia (King) Department of Paediatric Surgery, The Royal Children's Hospital, Melbourne, Australia (King) Department of Paediatrics, University of Melbourne, Melbourne, Australia (King, Heloury) Surgical Research, Murdoch Children's Research Institute, Melbourne, Victoria, Australia (Heloury) Department of Urology, The Royal Children's Hospital, Melbourne, Australia
Issue Date: 29-May-2017
Copyright year: 2017
Publisher: Elsevier Ltd
Place of publication: United Kingdom
Publication information: Journal of Pediatric Urology. 13 (2) (pp 158-163), 2017. Date of Publication: April 2017.
Journal: Journal of Pediatric Urology
Abstract: Introduction Leydig cell hyperplasia (LCH) and Leydig cell tumours (LCTs) in children are rare, typically presenting with precocious puberty. Previously, orchidectomy was the routine management; however, more recently, testis-sparing surgery has been performed with good results. We present a series of unusual presentations of LCH, raising new management questions, and a review of the literature regarding LCH and LCT in children. Study design We performed a literature search using Ovid Medline, PubMed, and Google Scholar, producing 456 articles. We reviewed all case reports and series containing paediatric patients, and relevant review articles. Results We report three cases of LCH, two of which were incidental findings. All three cases underwent testis-sparing surgery. In the literature there were seven cases of LCH and 101 cases of LCT in prepubertal children. The most common presentation was with precocious puberty. Three cases of LCH and more than two-thirds of LCTs were managed with orchidectomy and overall only 11% of the cases underwent testes-sparing surgery (24% did not specify operative management). There were no reports of recurrence or malignancy. Discussion Our case series presents three new clinical presentations of LCH that have not previously been reported in the literature: one of incomplete precocious puberty and two with incidental findings on ultrasound in asymptomatic children. Historically, children with the classic presentation of precocious puberty and a testicular lesion have been managed with orchidectomy. Nowadays, many clinicians advocate testes-sparing surgery given there have been no cases of malignancy. In children with no clinical or biochemical signs of precocious puberty, lesions identified on ultrasound can be safely monitored for a period of time. However, if the lesion does not regress, excisional biopsy is recommended to establish the diagnosis, ideally before the onset of puberty. Conclusion Leydig cell hyperplasia and tumours in pre-pubertal children are benign. Testes-sparing surgery with regular follow-up appears to be safe management.Copyright © 2017 Journal of Pediatric Urology Company
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1016/j.jpurol.2016.12.028
ORCID: Mennie, Nicole; ORCID: http://orcid.org/0000-0002-8980-3701
Link to associated publication: Click here for full text options
PubMed URL: 28238607 [http://www.ncbi.nlm.nih.gov/pubmed/?term=28238607]
ISSN: 1477-5131
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/38665
Type: Review
Subjects: lymphadenopathy
male
orchiectomy
precocious puberty
preschool child
priority journal
review
school child
testicular enlargement
testis biopsy
testosterone blood level
androstenedione/ec [Endogenous Compound]
testosterone/ec [Endogenous Compound]
*Leydig cell hyperplasia/et [Etiology]
*Leydig cell hyperplasia/su [Surgery]
pathophysiology
androstenedione blood level
case report
*cell hyperplasia/et [Etiology]
*cell hyperplasia/su [Surgery]
child
clinical examination
clinical feature
follow up
frozen section
hair growth
hematoma
histopathology
human
human tissue
immunohistochemistry
incidental finding
incision
inguinal pain
incidental finding
incision
inguinal pain
lymphadenopathy
male
orchiectomy
pathophysiology
precocious puberty
preschool child
priority journal
Review
school child
clinical examination
testis biopsy
testosterone blood level
child
*cell hyperplasia / *etiology / *surgery
case report
androstenedione blood level
testicular enlargement
clinical feature
follow up
frozen section
hair growth
hematoma
histopathology
human
human tissue
immunohistochemistry
Type of Clinical Study or Trial: Case series or case report
Appears in Collections:Articles

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