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Syringocystadenocarcinoma papilliferum: a case report.J
Korean Med Sci. 2007 Aug ; 22 (4):762-5.
Syringocystadenocarcinoma papilliferum (SCACP) is a rare form of
adenocarcinoma of the skin. This is the malignant counterpart of
syringocystadenoma papilliferum (SCAP) and usually develops on the
scalp in a long-standing lesion identified clinically as SCAP. We
describe a 65-yr-old Korean man with a nodule on the right supra-pubic
area with a 2-yr duration. Histologically this tumor had a similar
overall configuration as in SCAP, but the tumor was asymmetric and
poorly circumscribed, extending into the deep dermis and showed
cytologic atypia. The tumor cells showed positive reaction to
GCDFP-15, but negative reaction to CEA and HMFG-1. We established the
diagnosis of SCACP in the patient, and a wide excision was performed
to remove the tumor. The patient has been well without relapse or
metastasis for 2 yr.
Syringocystadenoma
papilliferum: report of 8 cases.
Pathologica. 2006 Jun;98(3):178-80.
Syringocystadenoma papilliferum (SCAP) is a rare cutaneous adnexal
neoplasm with variable clinical appearance and characteristic
histology. It arises in about one third of cases within a sebaceous
hamartoma (SH) and in this case, multiple other benign adnexal
neoplasms may be associated with it. We report the clinical and
pathological data of 8 cases of syringocystadenoma papilliferum. The
age at the time of the diagnosis varied from 3 to 48 years with an
average age of 28 years. Three tumors were localized in the scalp, 2
in the trunk, and 3 others of unusual locations: 1 in the eyelid, 1 in
the thigh and 1 in the popliteal fossa. Histopathological examination
revealed 3 SCAP occurring within SH. The SCAP observed in the eyelid
was associated with an apocrine cystadenoma without features of SH.
The four others were not associated with any other lesion. |
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Syringocystadenoma
Papilliferum
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Dermpath-India
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Congenital syringocystadenoma papilliferum.Pediatr
Dermatol. 2008 Jan-Feb;25(1):132-3.
We present a
boy with a congenital, ulcerated nodule on the scalp. At birth, the
lesion was considered to be the result of a traumatic injury, but a
biopsy at the age of 6 months pointed to a diagnosis of
syringocystadenoma papilliferum. We draw attention to the difficulty
of identifying head lesions in young children from clinical signs
alone.
Syringocystadenoma
papilliferum: report of first case on the pinna.
J Laryngol Otol. 2006 Dec;120 (12) :e45. Epub 2006 Nov 14.
Syringocystadenoma papilliferum is a benign adnexal skin tumour,
which, in a third of cases, arises from an organoid nevus on the
head and neck. We report on a 17-year-old man with a
syringocystadenoma papilliferum on his right pinna of three-years
duration. The clinical and histopathological features are described.
Following excision and skin grafting, the patient remains
asymptomatic four years after surgery. This is the first report of a
syringocystadenoma papilliferum on the pinna. |
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August 2009
Skin Tumours
Skin Adnexal (Appendage) Tumours
Benign Sweat Gland Tumours
Hamartomas
Chondroid syringoma
Syringoma
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