Multiple Perianal Epidermal Cysts Found in a Case of Lowe Syndrome: A Case Report and Review of the Literature.
Journal
The American journal of case reports
ISSN: 1941-5923
Titre abrégé: Am J Case Rep
Pays: United States
ID NLM: 101489566
Informations de publication
Date de publication:
24 Mar 2023
24 Mar 2023
Historique:
entrez:
24
3
2023
pubmed:
25
3
2023
medline:
28
3
2023
Statut:
epublish
Résumé
BACKGROUND Lowe syndrome, also known as oculocerebrorenal syndrome, is a rare genetic condition caused by an X-linked mutation of the OCRL1 gene, with an estimated prevalence in the general population of approximately 1 in 500 000. It is a multisystem disorder most commonly affecting the eyes, central nervous system, and kidneys. These commonly manifest as congenital cataracts, intellectual disability, and proximal renal dysfunction (Fanconi-type). Epidermal lesions are an uncommon manifestation of this condition, and the association is not completely understood. CASE REPORT Here we present a case of a 9-year-old boy with Lowe syndrome who presented with multiple cystic masses found in the perianal region. An excision was then performed to remove the masses and found that the lesions were epidermal cysts, which are infrequently found in Lowe syndrome. After excision, the patient recovered uneventfully without complications. CONCLUSIONS While epidermal cysts are an uncommon manifestation that have been documented, our case remains unique given the location and associated symptoms of the lesions. At presentation, the constellation of pain and perianal masses was concerning for a malignant etiology. However, after diagnostic imaging was performed, these lesions were found to be epidermal cysts, an infrequent manifestation of Lowe syndrome. Few previous case reports described cystic lesions in association with Lowe syndrome, and none, to our knowledge, have described multiple symptomatic perianal lesions. This case is important to consider because epidermal cystic lesions can be found with this presentation and should be considered on differential diagnoses for dermatologic findings in Lowe syndrome patients.
Identifiants
pubmed: 36959724
pii: 938248
doi: 10.12659/AJCR.938248
pmc: PMC10042271
doi:
Types de publication
Review
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e938248Références
J Histochem Cytochem. 2000 Feb;48(2):179-90
pubmed: 10639484
Traffic. 2014 May;15(5):471-87
pubmed: 24499450
Pediatr Nephrol. 2016 Dec;31(12):2201-2212
pubmed: 27011217
J Med Case Rep. 2019 Nov 2;13(1):325
pubmed: 31676009
Eur J Ophthalmol. 2020 Sep;30(5):966-973
pubmed: 32340490
Orphanet J Rare Dis. 2006 May 18;1:16
pubmed: 16722554
J Dermatol. 2017 Jan;44(1):105-107
pubmed: 27178641
J Pediatr Genet. 2013 Jun;2(2):53-68
pubmed: 27625841
Korean J Pediatr. 2014 Mar;57(3):140-8
pubmed: 24778696
Open Access Maced J Med Sci. 2018 Jan 10;6(1):28-30
pubmed: 29483974
Pediatr Dermatol. 2004 Jan-Feb;21(1):54-7
pubmed: 14871328
Ann Dermatol. 2010 Nov;22(4):444-6
pubmed: 21165217