2001
DOI: 10.1053/ejso.2000.1067
|View full text |Cite
|
Sign up to set email alerts
|

Metastatic malignant acrospiroma of the hand

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
25
0

Year Published

2004
2004
2017
2017

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 22 publications
(25 citation statements)
references
References 14 publications
0
25
0
Order By: Relevance
“…An uncommon variant is eruptive syringoma, a clinical condition characterised by multiple yellow-brown-coloured, firm papules, with no specific site predilection in young adults. 27 The pathogenesis of eruptive syringoma is controversial, and it has been suggested that it represents a reactive eccrine gland ductal proliferation following cutaneous inflammatory conditions. 28 There is also an increased incidence of eruptive syringoma in patients with Down's syndrome, and, rarely, syringomas can occur in familial form.…”
Section: Syringoma and Syringoid Eccrine Carcinomamentioning
confidence: 99%
“…An uncommon variant is eruptive syringoma, a clinical condition characterised by multiple yellow-brown-coloured, firm papules, with no specific site predilection in young adults. 27 The pathogenesis of eruptive syringoma is controversial, and it has been suggested that it represents a reactive eccrine gland ductal proliferation following cutaneous inflammatory conditions. 28 There is also an increased incidence of eruptive syringoma in patients with Down's syndrome, and, rarely, syringomas can occur in familial form.…”
Section: Syringoma and Syringoid Eccrine Carcinomamentioning
confidence: 99%
“…Although these tumors are rare, they can be locally aggressive and tend to have a poor prognosis 112 . Rates of metastases remain unknown, although a number of case reports describe lung, myocardial, and most commonly lymph node metastases 113–116 . These tumors tend to have a high rate of local recurrence 116,117 …”
mentioning
confidence: 99%
“…The prognosis of hidradenoma is often good but malignant transformation into hidradenosarcoma is possible, this risk is increased after the age of 50 years. The malignant form described by KEASBEY and HADLEY in 1954 [9] has an important local aggressiveness, with lymph node and bone metastases but can also be cutaneous, hepatic and pulmonary metastases to [10]. This malignant form often develops from a benign lesion but a de novo malignant hidradenoma is possible.…”
Section: Discussionmentioning
confidence: 99%