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Five cases
Deba P Sarma, MD
Omaha
Case 1
Apocrine hidrocystoma
F 45, mons pubis
Dermal cyst
Cyst wall is lined by apocrine-type epithelium with decapitation secretion
Apocrine hidrocystoma
Clinical:
Solitary cystic dermal lesion in face, eyelids, axilla, pubis,
prepuce.
Pathology:
Unilocular or multilocular dermal cyst.
Lined by double layers of cells: outer layer of flattened
myoepithelial cells and inner columnar cells with
decapitation secretion and dark basal nuclei.
Case 2
Apocrine hidrocystoma
M 80, right eyebrow
Apocrine hidrocystoma
F 84, left temple
Comment
Uncommon, solitary cyst derived from apocrine duct
occurring on the head and neck.
Unilocular or multilocular dermal cyst lined by two layers of
cells: an outer layer of flattened myoepithelial cells and an
inner layer of tall columnar cells with red cytoplasm and
basally placed nuclei.
Decapitation secretion is present. If significant papillary
epithelial projections are seen within the cyst, the lesion is
called an apocrine cystadenoma.
Case 4
Well circumscribed, encapsulated dark dermal tumor, not connected to the epidermis.
Dark dermal nodules resemble lymph node.
Tumor is composed of glandular structures lined by two layers of epithelial cells,
small dark cuboidal cells and large clear cells. Stroma shows lymphocytic
infiltration.
Glandular lumina contain pale eosinophilic material. Note
the small dark cells and large clear cells and lymphocytes.
Note the decapitation secretion by the apocrine type epithelium.
Focally, the apocrine type epithelium shows spectacular granular cell change.
END