Diagnosis of Path
Quiz Case 25:
Apocrine
hidrocystoma/Cystadenoma:
Adenomatous cystic proliferation of apocrine
glands. Some regard them as retension cysts, others regard some of these
lesions with epithelial proliferation as benign tumours - Apocrine
Cystadenoma.
Clinical presentation:
These may present as uni or multilocular cystic structures
containing clear or brownish fluid. It is suggested that the
pigmentation observed clinically is due to the Tyndall phenomenon.
ImageLink (JHU):

Site:
Located on the head and neck of older patients. Other sites include
trunk and genital region.
Microscopic features:
Cysts are lined by two layers of cells. The inner layer
consists of tall columnar cells with eosinophilic cytoplasm and showing
decapitation secretion. The outer layer consists of myoepithelial cells. The
apocrine cells probably contain lipofuscin granules. These granules are
PAS positive and diastase resistant.
Rarely, the lining epithelium shows papillary proliferation - Papillary apocrine
gland cyst. (D/D:
Hidradenoma papilliferum or
syringocystadenoma papilliferum.)
Immunohistochemistry:
Gross cystic disease fluid protein has been identified.
Apocrine hidrocystomas
grow gradually and usually do not recur after excision.
Image links: (Dr.Weems)
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