Basaloid/follicular hyperplasia overlying connective tissue/mesenchymal hamartomas simulating basal cell carcinomas

被引:12
作者
Stashower, ME [1 ]
Smith, K
Corbett, D
Skelton, HG
机构
[1] Natl Naval Med Res Inst, Dept Dermatol, Bethesda, MD USA
[2] Lab Corp Amer, Bethesda, MD USA
关键词
D O I
10.1067/mjd.2001.117727
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Basaloid hyperplasia has been described overlying dermatofibromas as well is in the epidermis overlying nevus sebaceus. Although the morphology of these areas may resemble-that of basal cell carcinoma (BCC), in the majority of cases aggressive behavior of the proliferation is not seen. In fact, the basaloid proliferation often shows follicular differentiation and may be stimulated and maintained by its relationship with the underlying stromal cells. Objective: We wanted to determine whether immunohistochemical staining for antibodies, which may suggest differences in pathogenesis, were different in basaloid hyperplasia overlying connective tissue/mesenchymal hamartomas and BCC. Methods: We report 3 cases of connective tissue/mesenchymal hamartomas with overlying basaloid hyperplasia, in which the areas of the basaloid proliferation showed Follicular differentiation. Immunohistochemical stains included Ber-EP4 PCNA, Ki-67, Bcl-2, p53, SM-Actin, CD31, Factor XIIa, KP-1, and CD34. Results: There was a diffuse positive reaction for Ber-EN in all specimens and there was increased nuclear staining for PCNA and Ki-67. There was focal cytoplasmic staining for Bcl-2 in the areas of basaloid hyperplasia. Immunohistochemical staining for p53 showed only scattered positive cells except in a small focus in the areas of basaloid hyperplasia. The connective tissue component of all lesions showed diffuse staining for CD34 surrounding areas of basaloid hyperplasia in the mesenchymal component as well as in abundant S-100(+) nerves. Conclusion: The areas of basaloid hyperplasia in these hamartomas exhibited an immature phenotype similar to that seen in both BCCs and follicular tumors; however, the patterns of proliferation markers, p53, Bcl-2, and the surrounding stromal cell markers were similar Lo those of benign follicular tumors. Thus the staining pattern for this group of antibodies suggests that areas of basaloid hyperplasia are not BCC.
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页码:886 / 891
页数:6
相关论文
共 12 条
[1]   Immunohistochemical nuclear staining for p53, PCNA, and Ki-67 in different histologic variants of basal cell carcinoma [J].
Barrett, TL ;
Smith, KJ ;
Hodge, JJ ;
Butler, R ;
Hall, FW ;
Skelton, HG .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 37 (03) :430-437
[2]   Follicular basal cell hyperplasia overlying dermatofibroma [J].
Cheng, L ;
Amini, SB ;
Zaim, MT .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (06) :711-718
[3]  
HAERSLEV T, 1995, ACTA DERM-VENEREOL, V75, P187
[4]  
JIMENEZ FJ, 1995, MODERN PATHOL, V8, P854
[5]   CD34 STAINING PATTERN DISTINGUISHES BASAL-CELL CARCINOMA FROM TRICHOEPITHELIOMA [J].
KIRCHMANN, TTT ;
PRIETO, VG ;
SMOLLER, BR .
ARCHIVES OF DERMATOLOGY, 1994, 130 (05) :589-592
[6]  
LANTIS S, 1968, ARCH DERMATOL, V29, P117
[8]   Metallothionein expression in basaloid proliferations overlying dermatofibromas and in basal cell carcinomas [J].
Rossen, K ;
Haerslev, T ;
HouJensen, K ;
Jacobsen, GK .
BRITISH JOURNAL OF DERMATOLOGY, 1997, 136 (01) :30-34
[9]   Immunophenotyping of dermal spindle cell tumors: Diagnostic value of monocyte marker Ki-M1p and histogenetic considerations [J].
Rudolph, P ;
Schubert, B ;
Wacker, HH ;
Parwaresch, R ;
Schubert, C .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 1997, 21 (07) :791-800
[10]   A review of tumor suppressor genes in cutaneous neoplasms with emphasis on cell cycle regulators [J].
Smith, KJ ;
Barrett, TL ;
Smith, WF ;
Skelton, HM .
AMERICAN JOURNAL OF DERMATOPATHOLOGY, 1998, 20 (03) :302-313