2009
DOI: 10.2478/v10042-009-0011-5
|View full text |Cite
|
Sign up to set email alerts
|

Advanced differentiation in trichoepithelioma and basal cell carcinoma investigated by immunohistochemistry against neurofilaments.

Abstract: Basal cell carcinoma (BCC) and trichoepithelioma (TE) are sometimes diagnostic challenges for the pathologist in terms of their differential diagnosis. Although literature is quite rich in information about histologic and immunohistochemical clues to distinguish the differences between both, no single finding must be completely reliable. Moreover, some consider that TE is a better differentiated follicular tumour, while BCC represents a less developed stage in differentiation. For instance, the latter opinion … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
7
0

Year Published

2010
2010
2023
2023

Publication Types

Select...
6
2

Relationship

0
8

Authors

Journals

citations
Cited by 11 publications
(7 citation statements)
references
References 20 publications
0
7
0
Order By: Relevance
“…Immunohistochemistry, if appropriately applied, can offer ancillary diagnostic support beyond that supplied by the evaluation of hematoxylin and eosin‐stained tissue sections. Numerous markers have been applied to this differential diagnostic setting, including bcl‐2, 3–8 Ki‐67, 8,9 proliferating cell nuclear antigen (PCNA), 8 lectins, 5,10,11 transforming growth factor‐beta, 4 stromelysin‐3, 12 p53, 8,9 p21, 9 CD10, 13 CD34, 4–6,14,15 Ber‐EP4 6,16 and neurofilament 17 . To date, cytokeratin‐20 (CK20), which highlights Merkel cells, has crystallized as the most useful marker 18–20 .…”
mentioning
confidence: 99%
See 1 more Smart Citation
“…Immunohistochemistry, if appropriately applied, can offer ancillary diagnostic support beyond that supplied by the evaluation of hematoxylin and eosin‐stained tissue sections. Numerous markers have been applied to this differential diagnostic setting, including bcl‐2, 3–8 Ki‐67, 8,9 proliferating cell nuclear antigen (PCNA), 8 lectins, 5,10,11 transforming growth factor‐beta, 4 stromelysin‐3, 12 p53, 8,9 p21, 9 CD10, 13 CD34, 4–6,14,15 Ber‐EP4 6,16 and neurofilament 17 . To date, cytokeratin‐20 (CK20), which highlights Merkel cells, has crystallized as the most useful marker 18–20 .…”
mentioning
confidence: 99%
“…Numerous markers have been applied to this differential diagnostic setting, including bcl-2, 3 -8 Ki-67, 8,9 proliferating cell nuclear antigen (PCNA), 8 lectins, 5,10,11 transforming growth factor-beta, 4 stromelysin-3, 12 p53, 8,9 p21,9 CD10,13 CD34, 4 -6,14,15 Ber-EP4 6,16 and neurofilament. 17 To date, cytokeratin-20 (CK20), which highlights Merkel cells, has crystallized as the most useful marker. 18 -20 Typically, only trichoepitheliomas but not basal cell carcinomas harbor Merkel cells in their tumor islands, although there are exceptions.…”
mentioning
confidence: 99%
“…This has thus driven an extensive effort to find an immunohistochemical marker of utility in differentiating the two. Immunohistochemical markers tested to date include CD34, 3,7-10 bcl-2, 3,9-12 CD10, 3,13 Ber-EP4, 10,14 androgen receptor (AR), 3,15,16 CK20, 3,16,17 stromelysin-3, 18 p53, 3,19,20 Ki-67, 3,19 p21, 19 transforming growth factor (TGF)-b, 21 lectins, 19,22 neurofilaments, 23 and p75 neurotrophin receptor. 24 None of these, to date, appears to be reliable in confidently differentiating desmoplastic trichoepithelioma from morpheaform/ infiltrative basal cell carcinoma (Table 1).…”
mentioning
confidence: 99%
“…2 MFTs are autosomal dominant affecting chromosome 9p21 with lesser expression and penetrance in a male. 1,6 The lesions of TE are characterized by firm skin-colored papules or nodules 2 to 8 mm in size, mainly concentrated around the nasolabial folds and forehead. The lesions first appear in childhood and may grow larger and increase in number over time.…”
Section: Discussionmentioning
confidence: 99%