April 2014
Volume 55, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2014
Giant Orbital Hydrocystoma in Children: Report of Three Cases
Author Affiliations & Notes
  • Mehrdad Malihi
    The Institute of Ophthalmology and Visual Sciences, New Jersey Medical School, Newark, NJ
  • Roger Turbin
    The Institute of Ophthalmology and Visual Sciences, New Jersey Medical School, Newark, NJ
  • Neena Mirani
    Department of Pathology, New Jersey Medical School, Newark, NJ
  • Paul D Langer
    The Institute of Ophthalmology and Visual Sciences, New Jersey Medical School, Newark, NJ
  • Footnotes
    Commercial Relationships Mehrdad Malihi, None; Roger Turbin, None; Neena Mirani, None; Paul Langer, None
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science April 2014, Vol.55, 5429. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Mehrdad Malihi, Roger Turbin, Neena Mirani, Paul D Langer; Giant Orbital Hydrocystoma in Children: Report of Three Cases. Invest. Ophthalmol. Vis. Sci. 2014;55(13):5429.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract
 
Purpose
 

Hydrocystoma (also known as sudoriferous cyst) is a benign cystic proliferation of a sweat gland found commonly on the eyelid skin of adults; we report three cases of giant orbital hydrocystoma in children, expanding the clinical and pathological spectrum of this entity.

 
Methods
 

Interventional case series.

 
Results
 

Case 1: An 8 year-old-boy presented with a 1 year history of painless progressive right proptosis. Computed tomographic and magnetic resonance imaging (MRI) revealed a well-defined, intraorbital, extraconal cystic lesion in the lateral orbit posterior to the globe causing bony erosion (Fig 1). Pathologic examination following total resection via lateral orbitotomy reveals a cystic lesion with a clear cavity lined by a smooth surface of a double layer of cuboidal cells, consistent with eccrine hydrocystoma. Case 2: A 13-year-old girl who had suffered blunt orbital trauma one year earlier developed a soft, mobile, non-tender subconjunctival mass in the temporal part of the right upper eyelid. MRI revealed a large well-defined cystic lesion in the right anterior orbit, which was later dissected from beneath the conjunctiva. Pathologic examination reveals a cystic cavity with papillary projections lined by two layers of cuboidal epithelial cells, with the innermost cells displaying eosinophilic cytoplasm and apical “snouting” (decapitation), characteristic of an apocrine hydrocystoma (Fig 2). Case 3: A two-month-old infant was noted to have a non-tender subconjunctival orbital growth visible in the medial left palpebral aperture. Surgical excision revealed a cystic lesion with a smooth internal surface. Microscopic evaluation revealed characteristics similar to case 1 and consistent with eccrine hydrocystoma.

 
Conclusions
 

Periocular hydrocystoma, which typically presents on the eyelid skin in adults, only rarely occur beneath the skin or conjunctiva: only 8 such lesions have previously been reported, 4 of them in the pediatric population. Presumably, the deeper location of these common skin lesions results either from embryonic rests or from traumatic implantation of glandular epithelium. All 4 previously reported pediatric cases were congenital and of apocrine subtype.Two of the cases in our series were of eccrine subtype, and one was traumatic in origin, expanding the clinical and pathological spectrum of this entity. Clinicians should be aware that an orbital cystic lesion in a child may represent a giant hydrocystoma.

   
Keywords: 631 orbit • 638 pathology: human  
×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×