Eruptive syringoma

Pruzan, D. L.

doi:10.1001/archderm.125.8.1119

Cited by 17 publications

(22 citation statements)

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“…In 19 cases the diagnosis of syringoma was a histological finding. This fact had already been observed in Pruzan's series, 30 including the prepubertal cases of eruptive syringomas in the differential diagnosis of papular dermatosis in children. From our studies we can conclude that the condition is as frequent in the prepubertal as in the postpubertal age, and it must be considered in the differential diagnosis of papular dermatosis at any age.…”

Section: Discussionsupporting

confidence: 56%

Eruptive syringoma: 27 new cases and review of the literature

Soler-Carrillo

Estrach

Mascaró

2001

Acad Dermatol Venereol

117

118

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Section: Discussionsupporting

confidence: 56%

Eruptive syringoma: 27 new cases and review of the literature

Soler-Carrillo

Estrach

Mascaró

2001

Acad Dermatol Venereol

117

118

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“…[1234] Recently, lower acrosyringium origin or the transitional portion between the acrosyringium and dermal duct have been also suggested as origins. [56] Syringoma typically appears around puberty and the women are most commonly affected.…”

Section: Discussionmentioning

confidence: 99%

“…[234] In a study by Patrizi et al ., 19 cases of 29 cases were eruptive which is more frequent in comparison to our series (19 from 34 cases). [1] Occasionally, however, generalized eruptive syringoma develops in a more widespread distribution.…”

Section: Discussionmentioning

confidence: 99%

“…Clinically, they appear as multiple, small, firm, skin-colored or slightly yellow soft papules, 1-3 mm in diameter, symmetrically distributed and usually asymptomatic. [1234] Eruptive syringoma is a rare variant that typically develops on the face, anterior surfaces of the neck, chest, abdomen, upper extremities and genitalia. Most studies emphasize that the diagnosis of syringoma, particularly eruptive syringoma, usually was not suspected clinically and the definitive diagnosis is made by histological examination.…”

Section: Introductionmentioning

confidence: 99%

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Cutaneous syringoma: A clinicopathologic study of 34 new cases and review of the literature

Ghanadan

Khosravi

2013

Indian J Dermatol

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Background:Syringoma is a benign adnexal tumor derived from intraepidermal eccrine duct.Aim:The aim of the study is to report the experience concerning syringoma by reviewing the clinical and histopathologic features of a series of 34 histologically diagnosed syringoma patients observed over a period of six years.Materials and Methods:Thirty-four patients were sorted into two groups, localized and generalized syringoma, according to the Friedman and Butler classification. Different histopathologic findings were recorded in specially designed questionnaires for further analysis.Results:Ninety-seven percent of the patients were females with the mean age of 27.6 years. The mean duration of the lesions before the presentations was six years. The diagnosis of syringoma was only considered in 23 patients (67.6%) and was the initial diagnosis in only 13 (38.2%) patients. All histological findings were seen more common in our cases. in comparison to the documented cases in the literature. Clear cell change of epithelial eccrine cells was 85.2% and there was no difference in the histopathological findings in the two groups. Our patients with generalized syringoma (GS) had a considerable lower age of onset than the ones with localized syringoma (LS) (P = 0.027).Conclusion:Our patients with generalized syringoma were younger than the ones with localized syringoma. Distribution of the generalized syringoma was mainly in the chest and neck followed by the forearms whereas localized syringoma was mostly confined to the face, axilla and genitalia. There were also some conditions associated with our cases including sarcoidosis, calcinosis cutis and basal cell carcinoma.

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“…They occur pre dominantly in women and may develop at any age, with a peak incidence between the third and fourth decades, although they are not rare in children [3], The most frequent clin ical variant is the one located on the infraocu lar areas in healthy people, but other clinical variants have been reported, as well as famil ial cases or associated with Down's syndrome [2][3][4].…”

Section: Discussionmentioning

confidence: 99%