Objective: Sclerosing sweat duct carcinoma (SSDC) is a rare, slow-growing,
locally invasive skin tumor of eccrine and pilar origin. It is usually loca
ted on the face, particularly the upper lip, cheek, and forehead. It has be
en infrequently reported on the eyelid, secondarily involved from adjacent
cheek and brow tumors. Only four previous cases have reported primary eyeli
d tumors. The authors present four cases of primary eyelid margin involveme
nt, which show the variability in clinical presentations.
Design: Retrospective case series, The authors present four case studies of
lower eyelid margin tumors diagnosed as SSDC,
Participants/Methods: The history of this recently recognized neoplasm is d
iscussed in relation to the cases presented and the role of the ophthalmolo
gist and pathologist in such cases.
Results: Primary SSDC of the eyelid margin is a reportedly rare entity. Thi
s particular presentation can occur in all age groups; can mimic benign, ac
anthotic, or basal cell-like tumors; and is usually misdiagnosed initially.
This can lead to a delay in definitive treatment for a tumor that classica
lly presents late in its natural history to health professionals. All eight
cases of primary eyelid SSDC now reported in the literature have occurred
in the lower lid.
Conclusion: This rare but aggressive tumor is difficult to diagnose from a
simple biopsy and may be more common than previously believed. Initial or e
arly diagnosis is important because of unusually invasive characteristics.
Recurrence is common and usually leads to extensive tissue loss via direct
invasion or subsequent wide resection, Correct histologic diagnosis at the
time of initial tumor removal will likely aid in achieving complete excisio
n with fewer recurrences.